Plant Genetics and Gene StudyView this Special Issue
Review Article | Open Access
Nikolai Borisjuk, Olena Kishchenko, Serik Eliby, Carly Schramm, Peter Anderson, Satyvaldy Jatayev, Akhylbek Kurishbayev, Yuri Shavrukov, "Genetic Modification for Wheat Improvement: From Transgenesis to Genome Editing", BioMed Research International, vol. 2019, Article ID 6216304, 18 pages, 2019. https://doi.org/10.1155/2019/6216304
Genetic Modification for Wheat Improvement: From Transgenesis to Genome Editing
To feed the growing human population, global wheat yields should increase to approximately 5 tonnes per ha from the current 3.3 tonnes by 2050. To reach this goal, existing breeding practices must be complemented with new techniques built upon recent gains from wheat genome sequencing, and the accumulated knowledge of genetic determinants underlying the agricultural traits responsible for crop yield and quality. In this review we primarily focus on the tools and techniques available for accessing gene functions which lead to clear phenotypes in wheat. We provide a view of the development of wheat transformation techniques from a historical perspective, and summarize how techniques have been adapted to obtain gain-of-function phenotypes by gene overexpression, loss-of-function phenotypes by expressing antisense RNAs (RNA interference or RNAi), and most recently the manipulation of gene structure and expression using site-specific nucleases, such as CRISPR/Cas9, for genome editing. The review summarizes recent successes in the application of wheat genetic manipulation to increase yield, improve nutritional and health-promoting qualities in wheat, and enhance the crop’s resistance to various biotic and abiotic stresses.
Cereals are a key component of human diets, providing a significant proportion of the protein and calories consumed worldwide. While rice and maize dominate global cereal production, wheat is another vital crop consumed by humans, contributing to approximately 20% of our energy needs (calories) and 25% of our dietary protein. The Green Revolution of the 1970s achieved enormous yield gains via the introduction of disease resistant semidwarf high yielding wheat varieties developed by Dr. N.E.Borlaug and colleagues. Since that time, however, global wheat production has stagnated, and current trends show that yields will not be sufficient to meet growing market demands.
According to the United Nations’ Food and Agriculture Organization (FAO), over 756 million tonnes of wheat grain was harvested from over 220 million ha of arable land in 2016/2017 (www.fao.org/faostat). Despite this, wheat lags behind other major cereals such as maize and rice, both in terms of yield, and the application of genomic tools for its improvement . While the average worldwide yield grew almost 3-fold during the Green Revolution, driven by the expansion of irrigation, intensive use of fertilisers and advanced breeding ; the current average global wheat yield of ~3 tonnes per hectare is far below the crop’s potential . In order to feed the population of 9 billion people predicted for 2050, wheat yield should grow by over 60% while still maintaining and/or improving its nutritional characteristics [3, 4]. To achieve this goal without increasing the area of cultivated land, which is simply not available, emphasis must be concentrated on key traits related to plant productivity and adaptation to environmental challenges. A deficit in this key staple crop could present a serious threat to global food security, so improved molecular-based breeding and genetic engineering techniques are necessary to break through the current yield ceiling.
Existing modern breeding efforts now need to be complemented with advanced crop functional genomics, which can provide insights into the functioning of wheat genetic determinants. The available tools for wheat genetic modification provide the experimental means to functionally characterize genetic determinants by suppressing or enhancing gene activities. This knowledge can then be used for targeted improvements tailored to the specific needs of the diverse and changing environments in which wheat is grown across the world. This offers the potential to tackle yield gaps wherever they exist, for a variety of causes, enabling this global crop to finally reach its full potential.
2. Progress in Wheat Genetic Transformation
Bread wheat (Triticum aestivum L.), the most widespread of all wheat species, is an annual herb belonging to the family Gramineae or Poaceae. Wheat was domesticated around 8,000 years ago  and has since undergone hybridization and genome duplication events to generate its hexaploid genome (2n = 6x = 42, AABBDD), which is more than five times larger than the human genome. It was previously estimated that the genome of common wheat contained over 128,000 genes , with over 80% of the genome consisting of repetitive sequences of DNA . However, more recent estimates suggested a total of 107,891 high-confidence genes with over 85% repetitive DNA sequences, representing a threefold redundancy due to its hexaploid genome .
Genetic transformation, the fundamental tool of genetic engineering, allows the introduction and expression of various genes of interest in the cells of living organisms, bypassing, when desirable, the barriers of sexual incompatibility that exist in nature. Despite the considerable efforts of the international research community, development of wheat genetic engineering lags behind that of the other key agricultural crops like rice and maize. This may be attributed to the genetic characteristics of wheat, including its very large (17,000 Mbp) and highly redundant complex genome, as well as the relative recalcitrance of most varieties to in vitro culture and regeneration (reviewed recently in ).
The first successful genetic transformation of common wheat was conducted at Florida University, USA , using biolistics and financed by a research grant from Monsanto. Scientists from Monsanto were also the first to report the generation of transgenic wheat using Agrobacterium-mediated transformation .
2.1. Wheat Transformation Methods
Presently, biolistics and Agrobacterium-mediated transformation using immature embryos as explants remain the main methods for genetic engineering of wheat. Each method has its own advantages and drawbacks (Table 1). The main advantages of Agrobacterium transformation are the relatively high ratio of single copy gene inserts and relative simplicity of the transformation procedure. In contrast, biolistics offer benefits in their capacity to transform organelles and deliver RNA, proteins, nanoparticles, dyes, and complexes into cells. Utilization of linear Minimal Expression Cassettes (MECs) in biolistic transformation enables the production of plants carrying much simpler patterns of transgene integration compared to plasmid bombardment, with a higher proportion of single copy inserts [36–38].
In addition, biolistic delivery of MEC simplifies the simultaneous cotransformation of several genes and, in contrast to Agrobacterium, does not introduce vector backbone DNA or repetitive border sequences flanking the T-DNA into the transformed plant cells. In experiments with the wheat cv. ЕМ12, transformation with MECs instead of plasmids improved transformation frequency (TF) almost threefold from 0.4% tо 1.1% . A simplified method for DNA/gold coating was described by Ismagul et al.  for the high-throughput biolistic production of single copy transgenic wheat utilizing diluted MECs. This method involves the application of PM solution (42% PEG 2000 and 560 mM MgCl2) instead of the spermidine and CaCl2 used in the standard Bio-Rad procedure.
Biolistics allow for the transfer into wheat of relatively large DNA fragments. Partier et al.  conducted successful biolistic transformation of wheat with a 53 Кb linear cassette which contained a 44 Kb fragment of an Arabidopsis gene flanked by selection and reporter genes. The intact cassette was detected in Т1 and Т2 generation plants. The main disadvantages of both Agrobacterium and biolistic transformation methods in wheat are genotype dependency, and the requirement for lengthy periods of aseptic tissue culture.
2.2. Wheat Transformation Frequencies
Until recently, the TF for most tested genotypes of common wheat remained quite low at a level mostly below 5% . Many research groups use model wheat varieties such as Bobwhite SH98-26 and Fielder in their experiments due to their amenability to transformation via published protocols [8, 9]. The cultivar Bobwhite SH98-26 was among 129 sister lines made from crosses of cultivars Aurora//Kalyan/Bluebird 3/Woodpecker at CIMMYT, and selected for its high TF of over 70% by biolistic transformation . Such high transformation efficiency is yet to be reproduced by other researchers, and although the reason for this remains unclear, it is possible that not all of the finer details of the transformation protocol could be described in the report. The success rate of this high TF may be explained by the particular hybrid genotype used, or simply the advanced skills and experience of the technicians at CIMMYT. Since publishing , A. Pellegrineschi has been employed by two big Biotech companies, Pioneer Hi Breed and Du Pont, which indirectly confirms that he has developed a reliable wheat transformation protocol that allowed him to produce the published results. The authors of the review are therefore not sceptical; however the high TF presented in  must be reproduced by other researchers in future if this protocol is to be widely adopted. The cultivar Fielder, which is the model variety in Agrobacterium transformation, was preselected by the researchers of the Japan Tobacco Company, where the detailed protocol “PureWheat” was developed  that allows TFs of 40–90%. In this protocol, positive selection through the application of phosphomannose isomerase (PMI), which converts mannose-6-phosphate into fructose-6-phosphate, was found to facilitate a relatively high TF (20%) in biolistic transformation of the spring wheat line UC703 .
2.3. Agrobacterium-Mediated Transformation
In recent years several groups have reported efficient Agrobacterium transformation of a number of wheat cultivars [8, 42–44]. Hensel et al.  developed a protocol to transform the model genotype Bobwhite SH98-26 with TFs up to 15%. In the experiments of Richardson et al.  using the PureWheat technology with the cv. Fielder, selection on 5-10 mg/l of phosphinothricin resulted in a TF of 41.0%. Without selective pressure, the TF was only around 2.3%. Similar results were obtained for Chinese commercial cultivars of wheat by Wang et al. , who demonstrated TF of 37.7% for cv. СВ037, 22.7% for cv. Kenong 199, and 45.3% for the model cv. Fielder. It was shown by Ishida et al.  that centrifugation of immature embryos before infection with Agrobacterium was one of the critical requirements for successful transformation, while heat shock, contrary to findings in other cereals, was not efficient. At present, Agrobacterium strains EHA101, EHA105 , AGL0, AGL1 [43, 45], GV3101 , C58C1 [47, 48], and LBA4404  are the most popular in wheat transformation.
Transformation using mature wheat embryos is currently characterized by relatively low TFs. Wang et al.  transformed longitudinally cut mature embryos and observed TFs of 0.06%, 0.67%, and 0.89% for the cultivars Bobwhite, Yumai 66, and Lunxuan 208, respectively. Aadel et al.  found that, with the application of 200 μМ acetosyringone, the TFs for the genotypes Rajae and Amal were 0.66% and 1.00%. The protocol of Medvecka and Harwood , using Bobwhite SH98-56, allows production of transformants at a TF of 2.2%. More information and a simplified protocol can be found in .
In contrast to in vitro methods, the in planta approach has the potential to overcome the problem of high genotype dependency seen with the existing transformation methods. There have been several publications on the in planta production of transgenic wheat, most involving the direct injection of Agrobacterium. Supartana et al.  reported agrobacterial transformation of wheat cv. Shiranekomugi using seeds soaked overnight in water. Transformation was achieved by double piercing the area where a shoot would later emerge with a needle dipped into Agrobacterium inoculum. This method used the Agrobacterium strains LBA4404 and an M-21 mutant strain, and no tissue culture steps were used at any stage. The plants obtained were analysed for antibiotic resistance, and by PCR, Southern hybridization and plasmid rescue to confirm their transgenic status. Zhao et al.  produced Agrobacterium-mediated transgenic wheat by adding inoculum to an incision made at the base of wheat seedlings. Their tissue culture-free method was reportedly successful in transferring a powdery mildew-resistance gene, with a TF of up to 9.82%. Similarly, in the experiments of Razzaq et al.  with the wheat cv. GA-2002, the apical meristems of imbibed wheat seeds were wounded and inoculated with the Agrobacterium strain LBA4404 containing the binary vector pBI121 (35S-GUS, pNOS-NPTII). The kanamycin resistant plants produced were analysed by PCR and GUS histochemical staining of the embryos. Risacher et al.  developed an efficient semi-in planta transformation protocol (US patent 7803988 B2, 2010) that involves in planta agrobacterial infection of immature embryos within developing seeds. Spikes of the spring wheat line NB1 were harvested 16 to 18 days after anthesis and Agrobacterium injected into the base of each spikelet. The spikes, with their flag leaves still attached, were incubated in low light for 2 to 3 days before embryos were isolated and cultured in vitro. The protocol achieved an average TF of 5% with 30-50% of plants carrying a single transgene insertion.
The practice of dipping floral buds in a suspension of Agrobacterium (Floral dip) is a routine and highly efficient method of transformation in Arabidopsis, but it is rarely successful in other plant species. However, Zale et al.  were able to generate three independent transgenic lines of the spring wheat line, Crocus, by utilizing the floral dip approach. The transformants were studied thoroughly at the molecular level for three to six generations. In their most recent publication, Hamada et al.  trialled a biolistic method for in planta transformation. They found that bombarding the exposed shoot apical meristems of the wheat cultivars Fielder and Haruyokoi, using 0.6 μm gold particles and 1350 psi pressure, resulted in the integration of the GFP reporter gene into the germline cells in 62% of regenerated plants (transformants), including possible chimeric individuals. The full potential of the wheat in planta procedures published to date is yet to be fully realized.
Microspore transformation using immature pollen grains is a method that generates doubled haploid homozygous wheat plants in a single generation. The great advantage of this technique is that it by-passes the several years required by other transformation methods to develop true-breeding transformant lines. Current protocols for microspore-based transgenic wheat production through electroporation, biolistics, and Agrobacterium-mediated transformation are presented in [55–57]. Various wheat genotypes have been used as donors. Express, Chris, Farnum, Hollis, Louise, Perigee, and WestBred 926 have all performed successfully in microspore transformation. Four genes were targeted for microspore transformation, including β-glucuronidase (GUS), uidA; bialaphos resistance, Bar; Trichoderma harzianum endochitinase gene, ThEn42; and Bacillus subtilis 1,4-β-xylanase gene [55–57]. In general, Agrobacterium-mediated microspore transformation produces the best outcome, generating stable homozygous plants and fewer chimeric plants. Given the value of doubled haploid lines in simplifying and accelerating wheat breeding, it is likely that microspore methods will be optimized in the future.
Recent advances in high-throughput sequencing technologies have allowed for more detailed information to be obtained about the composition and fate of transgenes introduced into plant cells through Agrobacterium-mediated transformation. In one report, close to 0.4% of transgenic Arabidopsis lines examined contained insertions of Agrobacterium chromosomal DNA . Singer et al.  showed, for the first time, the presence in transgenic plant cells of the extra-chromosomal circular T-DNA that they named “T-circles”. In rice, 26% of 331 analysed transgenic lines contained the transposon Tn5393, which was transferred from the Agrobacterium strain LBA4404 . This transposon was not detected in the strains EHA105 and GV3101. These data reflect the importance of detailed molecular analysis of transgenic lines, and careful selection of the appropriate agrobacterial strains for transformation. A better understanding of the biological mechanisms of the transfer and integration of transgenes during bacterial infection will also permit the creation of new more efficient strains of Agrobacterium [5, 60] or utilization of bacterial species that are not pathogenic in nature .
2.4. Optimization of Tissue Culture Conditions
Tissue culture conditions are important factors that impact the TF of all plants, including wheat. Below we present information reflecting the current trends in wheat tissue culture that might be of interest to researchers working in the field. Changing the composition of the macrosalts in the growth medium can positively affect the TF. Callus induction on 6x DSEM medium with an increased concentration of ammonium nitrate (62.56 mM) as the sole nitrogen source, resulted in the sevenfold improvement of TF during biolistic transformation of the elite wheat cv. Superb . The authors point out that this modification of the medium brought about an increase in the number of somatic embryoids and possibly also reduced stress during the bombardment of the cells due to the elevated osmolarity. Ishida et al.  identified some critical points in the transformation process and developed a detailed protocol for Agrobacterium-mediated transformation for both immature and mature wheat embryos from amenable genotypes. The authors however did not discuss any work on media improvements.
Antioxidants such as ascorbic acid, glutathione, lipoic acid, selenite, and cysteine were found to decrease necrosis and darkening of the tissues, improving plant regeneration and TF during genetic transformation . Lipoic acid at 25–50 μМ led to a twofold improvement in agrobacterial transformation of the wheat cv. Bobwhite .
Arabinogalactan-proteins at a concentration of 5 mg/l improved regeneration of bread (cv. Ikizce-96) and durum (cv. Mirzabey) wheat from 77.77% and 72.11%, to 94.86% and 89.73%, respectively . Kumar et al.  were able to achieve close to 100% plant regeneration from calli induced from wheat mature and immature embryos on 2.0 mg/l picloram, using a regeneration medium with 0.1 mg/l 2,4-D, 5.0 mg/l zeatin, and 15 mg/l CuSO4. Miroshnichenko et al.  developed a protocol for the regeneration of einkorn wheat (Т. monococcum L.), in which a combination of 3.0 mg/l dicamba, 50.0 mg/l daminozide (an inhibitor of ethylene synthesis), and 0.25 mg/l thidiazuron in the regeneration medium was the most efficient. The authors presume that this protocol may be useful for other wheat species as well.
2.5. Transient Transformation
Transient transformation with the use of reporter genes such as GUS  and GFP  is helpful for optimization of transformation conditions, as well as the analysis of promoters and protein expression. Transgene expression that is tightly targeted to specific tissues and developmental stages is often desired for directed modification of morphogenic traits. It can also be beneficial for avoiding feedback mechanisms, transgene silencing, or other unforeseen effects that can arise from constitutive transgene expression. Transient assays using protoplasts can also facilitate efficient analysis of gene regulatory mechanisms through cotransformation of enhancer/represser elements and promoter-reporter gene constructs . Viral induced gene silencing (VIGS) offers a fast and rapid transient assay for silencing of gene expression. VIGS can be achieved through a simple vacuum-aided cocultivation of germinated wheat seeds with Agrobacterium carrying an appropriate VIGS construct . However, results from VIGS are not comparable to results from stable transformation experiments, but this does not mean that the VIGS findings are false or of no value. Like RNAi, VIGS findings are useful for increasing our understanding of gene function and may lead to the development of a strategy that is more successful than simple constitutive transgene overexpression.
2.6. Future Directions: Gene Stacking and Plant Artificial Chromosomes
Gene stacking or pyramiding (defined as the stacking of multiple transgenes at a single chromosomal location) greatly expands the potential for genetic engineering of traits in wheat . Applications of this technology include modifying complex and multigenic traits, or inserting entire biosynthetic pathways, with integration at a single locus. This significantly simplifies the subsequent breeding process. Alternatively, for disease resistance traits, transgene stacks can aid in generating broad spectrum resistance to multiple threats, or more long-lasting defence to a single pathogen via genes with differing modes-of-action. Construction of a transgene stack is most often achieved using type II restriction enzymes in the Golden-Gate cloning system, or by Gibson Assembly. The integration of longer DNA fragments carries certain risks, however, such as reduced TF, fragmentation leading to only partial integration, and transgene silencing if promoters or other regulatory elements are used repeatedly. The magnitude of these risks differs according to the nature of the vectors or transformation cassettes, the transgene products, and the recipient genotype. Much of the more recent work involving stacked transgenes uses site-specific nucleases so that the transgene stack can be directed to a favourable locus in the genome. Site-specific nucleases will be covered in a later section of this review.
Plant artificial chromosomes or minichromosomes were also developed for multigene transfer . The main advantage is that they generate a new genetic locus that segregates independently of endogenous chromosomes, thus lessening the disruption of existing genomic regions. Minichromosomes have been developed in mammalian cells through a process named “Telomere-mediated chromosome truncation” that targets highly conserved telomeric repeat sequences. Analogous sequences have been identified in Arabidopsis, but progress in developing plant minichromosomes still lags behind the work in mammalian cells. Minichromosomes have the potential to act as “super-vector platforms” for the organization and expression of foreign genes and may even be designed with Cre/lox recombination sites to accept the introduction of new genes. This presents the option to “add on” additional alleles or genetic elements at a later date. Currently, the reliable transmission of minichromosomes to the progeny of primary transformants presents the greatest barrier to the application of this technology. However, initial work has suggested that wheat’s allopolyploid nature makes it more tolerant to chromosomal truncation than that of diploid species, making this a very promising future prospect for wheat genetic engineering .
3. Manipulating Agronomic Traits by Transgene Expression in Wheat
Built on the progress made on techniques for genetic manipulation of wheat, overexpression of endogenous and foreign genes has tremendously enriched our understanding of the functionality of numerous genes, contributing to the generation of many new and improved agronomically important traits. This improved understanding of gene function has led to the development of specific promoters to drive gene expression in response to environmental stimuli and/or in a tissue, organ, or developmental stage-specific manner [74, 75]. Various signals for directing expressed proteins to particular cellular compartments have also been used . Also, the field received another major stimulus through the use of transcription factors that function as major regulators of gene networks involved in numerous metabolic/physiological pathways. Transcription factors are often highly conserved between different plant species, so the information obtained from studying model plants like Arabidopsis or rice can be applied to other plants such as wheat [77–79].
In pursuit of improved crop performance, wheat genetic manipulations made by transgenic gene expression have targeted all major agronomic traits including yield, grain quality, and tolerance to abiotic and biotic stresses. The last 10 years have been characterized by acceleration in this field and an increasing number of publications. In this review we will focus primarily on attempts to improve yield and grain quality, the two areas that have not been sufficiently reviewed by other authors. For readers interested in improving wheat stress responses, we refer to recent comprehensive reviews on the topics of pathogen resistance [80–82] and abiotic stress tolerance [83, 84], as well as a recent review of transgenic wheat engineered with various genes of agronomic importance .
Yield is determined by the number and size of grains produced by the crop. The major genes controlling yield-related traits in wheat have been identified by genetic and genomics techniques, as reported in recent reviews [85–87].
Grain size (GS) has long been a focus of wheat selection and modern breeding . Progress in comparative wheat genomics has led to the identification of TaGW2 , a wheat homolog of a rice gene that negatively influences GS through regulation of cell division within the spikelet hull . The first experiments aimed at downregulating TaGW2 in wheat have shown some controversial results. Bednarek et al.  demonstrated that expression of a specific RNAi to suppress three TaGW2 homologs A, B, and D, of bread wheat cv. Recital, led to a decrease in grain size and weight. In contrast, Hong et al. , in a similar series of experiments, demonstrated a significant increase in the grain width and weight of a Chinese bread wheat cv. Shi 4185 that is typically characterized by small grains. Such differences in the phenotypes obtained in these two studies may be explained by a cultivar-specific reaction to experimental intervention, and/or by the application of different transformation protocols, as has been previously reported for barley .
Plant growth and productivity to a large extent relies on the uptake of carbon, nitrogen, and phosphorus. Ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBisCo), the most abundant protein on Earth, is the major enzyme assimilating atmospheric carbon in the form of CO2 into organic compounds in photosynthetic organisms. However, the enzyme has relatively low efficiency and a slow turnover rate . Despite significant progress in characterizing the enzyme’s properties  and improving RuBisCo efficiency in a range of plant species [96, 97], little success has been achieved so far in commercial crops, including wheat. Another area for optimizing carbon assimilation in crops is to introduce components of the C4 photosynthetic apparatus into C3 plants like wheat and rice. C4 plants, such as maize, display definite advantages over plants with C3 photosynthesis, especially under high temperature and limited water conditions . These advantages rely on a number of specific enzymes associated with RuBisCo, which provide higher photosynthetic efficiency and CO2 assimilation for the C4 plants. Transferring genes encoding the C4-specific enzymes, phosphoenolpyruvate carboxylase (PEPC), and pyruvate orthophosphate dikinase (PPDK) has led to promising results in rice  and wheat [100, 101]. As an example, Zhang et al.  generated transgenic wheat plants overexpressing PEPC and PPDK both separately and simultaneously in the same transgenic lines. The authors showed a positive synergistic effect on wheat photosynthetic characteristics and yield in the latter design. The follow-up study on wheat expressing maize PEPC demonstrated that, in addition to increased yield, the transgenic lines had improved drought tolerance linked to elevated expression of proteins involved in photosynthesis and protein metabolism .
The maize gene encoding the transcription factor Dof1, known to upregulate the expression of PEPC, was introduced into wheat by Agrobacterium-mediated transformation . Expression of ZmDof1 under the control of the light-inducible RuBisCo promoter, led to increased biomass and yield components in transgenic wheat, while constitutive expression resulted in the downregulation of photosynthetic genes and a corresponding negative impact on crop productivity.
The Nuclear Factor Y (NF-Y) transcription factors are recognized as important regulators of many plant developmental and physiological processes . NF-Ys are composed of protein subunits from three distinct transcription factor families (NF-YA, NF-YB, and NF-YC), with each of them represented by multiple members . TaNFY-A-B1, a low-nitrogen- and low-phosphorus-inducible NF-YA transcription factor, was overexpressed in wheat. This led to a significant increase in nitrogen and phosphorus uptake and grain yield in a field experiment . The authors suggested that increased nutrient uptake resulted from stimulated root development and upregulation of both nitrate and phosphate transporters in the roots of the transgenic wheat. Our own work showed the positive role of the second wheat gene, TaNF-YB4, in wheat grain yield . Constitutive overexpression of the gene under the control of the maize ubiquitin promoter in transgenic wheat cv. Gladius, resulted in the development of significantly more spikes, and a 20–30% increase in grain yield compared to the untransformed control plants.
Overexpression of another wheat transcription factor, TaNAC2-5A, which plays a role in nitrogen signalling, enhanced root growth and the nitrate influx rate, consequently increasing the root’s ability to acquire nitrate from the soil. Transgenic wheat lines revealed higher grain yield and higher nitrogen accumulation in aerial parts of the plant, which was subsequently allocated to grains .
Recently, a US research group reported on the expression of a rice gene encoding a soluble starch synthase gene (OsSS-I) with increased heat stability. This lead to a significant, 21-34%, yield increase in T2 and T3 generations of transgenic wheat under heat stress conditions . The expression of OsSS-I also prolonged the duration of the photosynthetic growth period in bread wheat. Similarly, overexpression of an endogenous gene coding for the chloroplastic glutamine synthase gene (TaGS2) in wheat led to prolonged leaf photosynthesis, and an increased rate of nitrogen remobilization into grains, which translated to higher spike number, grain number per spike, and total yield . Taken together, these reports on the modulation of carbon and nitrogen pathways once again illustrate the tight link between nitrogen assimilation and carbon metabolism  and resulting crop productivity.
3.2. Grain Quality
Grain is the harvested part of the wheat plant and its nutritional and health properties are determined by its biochemical composition. Starch, making up 55–75% of total dry grain weight, and storage protein 10–15%, are the main reserves of the wheat seed. Therefore, starch and protein greatly affect the quality of the products made from wheat flour. Along with optimized starch and protein, an adequate level of essential elements like iron, zinc, calcium, phosphorus, and antioxidants is also essential for healthy and balanced wheat products. Many of those quality traits have been addressed in recent years by means of transgenic interventions.
A number of studies have focused on the biosynthetic pathways and composition of starch, as reviewed by Sonnewald and Kossmann  and more recently by Kumar et al. . Based on the insights gained, a number of biotechnological interventions have been undertaken in order to both increase the amount of starch, and modulate its quality, with mixed outcomes. In an attempt to increase the level of precursors for starch synthesis in wheat, Weichert et al.  overexpressed the barley sucrose transporter gene (HvSUT1), which led to enhanced sucrose uptake and protein content in wheat grains, but no significant modification to starch levels. Expression of an optimized maize ADP-glucose pyrophosphorylase (ZmAGPase) resulted in elevated yield and enhanced photosynthetic rates in the transgenic wheat lines . Downregulation of the transcription factor TaRSR1, a wheat homolog of Rice Starch Regulator (OsRSR1), which was shown to negatively regulate the gene expression of some starch synthesis-related enzymes in wheat grains , resulted in a significant 30% increase in starch content, and also a ~20% increase in yield in terms of 1000-kernel weight . The increases in starch and yield were underpinned by the marked induction of expression of many key-genes in sugar metabolism and starch biosynthesis.
Starch consumer quality depends mostly on the ratio of amylose to amylopectin, the two main macromolecules forming starch. Starch with increased amylose has attracted much interest because of its contribution to resistant starch (RS) in food, which confers beneficial effects on human health. There is evidence that RS can provide protection from several health conditions such as diabetes, obesity, and cardiovascular diseases . A number of experiments focused on downregulation of starch branching enzymes, SBEIIa, and SBEIIb, which led to substantially increased amylose levels in wheat [119, 120]. High amylose starch has demonstrated positive health-related effects in rats  and more recently in a study involving obesity in humans .
Nitrogen is not only the most important plant nutrient contributing to crop yield, but also plays a significant role in defining the accumulation and, to some extent, the composition of storage protein in wheat grains . Nitrogen is supplied to the grain by two major pathways: remobilization from the canopy (leaves and stems), and root uptake from the soil. In their experiments, Zhao et al.  identified a novel wheat gene, TaNAC-S, a member of the NAC transcription factor family, that showed decreased expression during leaf senescence but significant expression in a stay-green phenotype. Transgenic overexpression of the gene in wheat resulted in delayed leaf senescence and increased protein concentration in grains, while the crop’s biomass and grain yield remained unaffected. Another group of Chinese researchers overexpressed a tobacco nitrate reductase gene (NtNR) in two commercial winter wheat cultivars, ND146 and JM6358, following Agrobacterium-mediated transformation . Constitutive overexpression of the gene remarkably enhanced foliar nitrate reductase activity and resulted in significantly augmented seed protein content and 1000-grain weight in the majority of the T1 offspring analysed.
The main component of wheat storage proteins, gluten, primarily determines the viscoelastic properties of wheat dough . Glutens consist of gliadins and glutenins, which together comprise 70-80% of the total flour protein. Therefore, genes encoding different classes of storage proteins have been targeted in efforts to improve both the nutritional value and bread-making quality of wheat. In fact, the genes coding for high-molecular glutenin subunits (HMW-GS) were among the first introduced into wheat [126–129], with the aim of improving dough functions following the first reports of a method for wheat transformation. Specifically, introduction of the subunits 1Ax1 and 1Dx5 into several common wheat cultivars by genetic transformation has demonstrated the potential of the transgenes to enhance dough quality to various extents [130–132]. In follow-up studies, the HMW-GS genes were introduced into selected wheat cultivars, mostly via the easily transformed cv. Bobwhite and then transferred into selected elite commercial varieties. Improvements in dough properties were obtained, demonstrating the feasibility of utilizing transgenic lines in wheat breeding programs [133, 134].
In contrast to HMW glutenins, which form complex polymer structures and are strongly correlated to dough elasticity, gliadins are monomeric components that contribute mainly to the extensibility and viscosity of the dough . Based on their electrophoretic mobility, gliadins are grouped into three structural types: α-, γ-, and ω-gliadins, each encoded by tightly-linked multigene clusters. The interest in genetic modification of gliadins has been stimulated, not only by their contribution to dough quality, but also because they include the majority of immunogenic epitopes related to immune conditions such as wheat-dependent exercise-induced anaphylaxis (WDEIA) and coeliac disease [136, 137].
Iron and zinc are essential micronutrients for human nutrition. According to the World Health Organization, over a billion people suffer from iron-deficiency anaemia, and Zn-deficiency is estimated to be associated with an annual death rate of almost half a million children under the age of five. Modern elite wheat cultivars usually contain suboptimal quantities of micronutrients , and because most of it is accumulated in the outer husk, aleurone, and embryo, the micronutrients are lost during milling and polishing . Another problem is that phytic acid, a major antinutritional factor for iron and zinc uptake in the human digestive tract, is codeposited with the minerals in aleurone storage vacuoles.
Biofortification, the enhancing of crop nutritional quality, is considered a promising approach to alleviate micronutrient deficiency. Transgenic studies have made significant headway in the development of strategies aimed at improving the available content of micronutrients such as iron in wheat grains. Plants store iron primarily in the form of ferritin structures accumulated mainly in nongreen plastids, etioplasts, and amyloplasts. Expression of a gene coding for an Aspergillus niger phytase, a phytic acid degrading enzyme targeted to the wheat aleurone , and endogenous  or soybean  ferritin genes in wheat endosperm, were the first successful attempts to transgenically biofortify wheat grains with iron. Recently, Connorton et al.  have isolated, characterized, and overexpressed two wheat Vacuolar Iron Transporter (TaVIT) genes under the control of an endosperm-specific promoter in wheat and barley. They reported that the introduction of one of the genes, TaVIT2, resulted in a greater than twofold increase in iron in the flour prepared from transgenic wheat grains without other detected changes.
4. RNA Interference Applications in Wheat
RNA interference (RNAi) is a common regulatory mechanism of gene expression in eukaryotic cells that has become a powerful tool for functional gene analysis and the engineering of novel phenotypes. The technique is based on the expression of antisense or hairpin RNAi constructs, or other forms of short interfering RNA molecules to direct posttranscriptional gene silencing in a sequence specific manner.
The vernalisation gene, TaVRN2, was the first wheat gene to be targeted by RNAi in transgenic wheat plants . TaVRN1 mRNA in transgenic plants was reduced by 60%, which led to much earlier flowering. In another study, Loukoianov et al.  suppressed expression of TaVRN1 by up to 80%, delaying flowering time by 14 to 19 days and increasing the number of leaves relative to the nontransgenic controls. These two breakthrough studies provided essential evidence for understanding the molecular mechanisms of flowering timing and vernalisation requirements in wheat, which may assist in diversifying the environments in which wheat can be grown.
The application of RNAi has made a solid contribution to manipulating wheat grain size [146–148] and quality [119, 149–151]. For example, Alterbach and Allen  used RNAi silencing to suppress the expression of ω-gliadins associated with WDEIA in the US wheat cv. Butte 86. They later demonstrated that transgenic wheat lines deficient in ω-gliadins had no changes in patterns of other grain proteins, and even showed increased protein stability with improved dough properties under various growth conditions . Similarly, Gil-Humanes et al.  downregulated the γ-gliadin genes in the wheat cv. Bobwhite and then transferred the trait into three commercial wheat cultivars by conventional crossing.
The reduction of γ-gliadins in wheat grains was compensated by an increased amount of glutenins, which led to stronger dough with better over-mixing-resistance. In a recent comprehensive study, Barro et al.  used a combination of seven RNAi expressing plasmids to selectively target α-, γ-, and ω-gliadins, and Low Molecular Weight (LMW) glutenins in the wheat cv. Bobwhite, with the goal to reduce gluten epitopes related to coeliac disease (CD). The protein analyses showed that three RNAi plasmid combinations resulted in total absence of CD epitopes from the most immunogenic α- and ω-gliadins in the transgenic wheat lines. These very promising results pave the way to developing wheat varieties with nonallergenic properties.
However, the major application of RNAi technology for wheat has been in pathogen and pest control using virus- and host-induced gene silencing platforms . A recent strategy, referred to as host-induced gene silencing (HIGS), has been developed to silence pest or pathogen genes by plant-mediated RNAi during their feeding or attempted infection, thereby reducing disease levels. This strategy relies on the host-plant’s ability to produce interfering RNA molecules complementary to targeted pest/pathogen genes. These molecules are then transferred to the invader, causing silencing of the targeted gene. In wheat, HIGS has been most widely applied to control fungal and insect diseases. As an example, silencing of fungal glucanosyltransferase genes (GTF1 and GTF2), and the virulence effector gene Avra10, affects wheat resistance to the powdery mildew fungus Blumeria graminis . Three hairpin RNAi constructs corresponding to different regions of the Fusarium graminearum chitin synthase gene (Chs3b) were found to silence Chs3b in transgenic F. graminearum strains. Coexpression of these three RNAi constructs in two independent elite wheat cultivar transgenic lines, conferred high levels of stable and durable resistance to both Fusarium head blight and Fusarium seedling blight . Stable transgenic wheat plants carrying an RNAi hairpin construct against the β-1, 3-glucan synthase gene FcGls1 of F. culmorum, or a triple combination of FcGls1 with mitogen-activated protein kinase (FcFmk1) and chitin synthase V myosin-motor domain (FcChsV), also showed enhanced resistance in leaf and spike inoculation assays under greenhouse and near-field conditions, respectively .
In other examples of RNAi, targeting the myosin-5 gene (FaMyo5) from F. asiaticum provided disease resistance in wheat . In further examples, wheat transformed with a vector expressing a double-stranded RNA, targeting the mitogen-activated protein kinase kinase gene (PsFUZ7) from Puccinia striiformis f. sp. tritici exhibited strong resistance to stripe rust . Transgenic wheat plants expressing siRNAs targeting the catalytic subunit protein kinase A gene from P. striiformis f. sp. Tritici, displayed high levels of stable and durable resistance throughout the T3 to T4 generations . Stable expression of hairpin RNAi constructs with a sequence homologous to mitogen-activated protein‐kinase from P. triticina (PtMAPK1), or a cyclophilin (PtCYC1) encoding gene, in susceptible wheat plants showed efficient silencing of the corresponding genes in the interacting fungus, resulting in disease resistance throughout the T2 generation .
The grain aphid (Sitobion avenae) chitin synthase 1 gene (CHS1) was also targeted with HIGS. After feeding on the representative T3 transgenic wheat lines, CHS1 expression levels in grain aphid decreased by half, and both total and moulting aphid numbers reduced significantly . Other target genes used for the control of grain aphids by RNAi in transgenic wheat were lipase maturation factor-like2 gene from pea aphid Acyrthosiphon pisum , carboxylesterase gene , Hpa1 , and a gene encoding a salivary sheath protein . Feeding on these transgenic plants resulted in significant reductions in survival and reproduction of aphids. It seems that the scope of RNAi-induced pest and disease resistance is as broad as the number of different pathogen and pest species that infect and cause damage to wheat.
5. Site-Specific Nucleases for Targeted Genome Modifications in Wheat
Targeted genome engineering using nucleases, such as zinc finger nucleases (ZFNs) and TAL effector nucleases (TALENs), were developed in the late century as innovative tools to generate mutations at specific genetic loci . Nuclease-based mutagenesis relies on induced site-specific DNA double-strand breaks (DSBs), which are either repaired by error-prone nonhomologous end joining (NHEJ), or high-fidelity homologous recombination (HR). The former often results in insertions or deletions (InDels) at the cleavage site leading to loss-of-function gene knockouts, whereas the latter leads to precise genome modification. In 2012, the field of eukaryotic genome editing was revolutionized by the introduction of CRISPR/Cas9 (bacterial Clustered Regularly Interspaced Short Palindromic Repeats) technology . This technology confers targeted gene mutagenesis by a Cas9 nuclease that is guided by small RNAs (sgRNAs) to the target gene through base pairing. This is in contrast to the DNA-recognition protein domain that must be specifically tailored for each DNA target in the case of ZFNs and TALENs. Because of its universality and operational simplicity compared to ZFNs and TALEN genome editing systems, CRISPR/Cas9 has rapidly superseded these earlier editing systems and been adopted by the majority of the scientific community [170, 171].
In wheat, the principal applicability of CRISPR/Cas9 was demonstrated in protoplasts and suspension cultures, where multiple genes were successfully targeted in the year following the publication of the original CRISPR/Cas9 principle [172–174]. Original methods for plant genome editing rely on the delivery of plasmids carrying cassettes for the coexpression of Cas9 and sgRNA, either by Agrobacterium or particle bombardment. For gene editing in wheat, a Cas9 protein containing one or more signals for nuclear localization is expressed from a codon optimized gene under the control of RNA polymerase II promoters such as CaMV35S or ZmUbi, while the sgRNA is usually expressed from a polymerase III promoter (most commonly, rice or wheat U6 and U3 promoters).
One of the additional advantages of the CRISPR/Cas9 system is its potential for multiplexing, i.e., the simultaneous targeting of several genes with a single molecular construct. Multiple sgRNAs can be introduced either as separate transcription units, or in polycistronic form . In bread wheat, editing has been reported in PEG-transfected protoplasts [172, 173, 176–178], electroporated microspores , and cell suspension cultures transformed by Agrobacterium . Edited wheat plants have been regenerated from immature embryos, immature embryo-derived callus, or shoot apical meristems transformed via particle bombardment [176, 177, 180–184] or Agrobacterium [185, 186].
Recently, protocols for DNA-free editing of wheat by delivering in vitro transcripts, or ribonucleoprotein complexes (RNPs) of CRISPR/Cas9 by particle bombardment, have been developed [176, 177]. The authors claim that these methods not only eliminate random integration of the CRISPR/Cas9 coding DNA elements into the targeted genome, but also reduce off-target effects. Thus, these advances allow for the production of completely transgene-free mutants in bread wheat with high precision. The main limitation of these transgene-free protocols is the lack of selection in the transformation and regeneration process. Another optimized delivery system has been developed by Gil-Humanes et al. . Here the authors used replicated vectors based on the wheat dwarf virus (Geminiviridae) for cereal genome engineering. It was shown that, due to increased copy number of the system components, virus-derived replicons increase gene targeting efficiency greater than 10-fold in wheat callus cells and protoplasts, compared to the nonreplicating control. The virus-based CRISPR/Cas9 system also promoted multiplexed gene targeted integration in different loci of the polyploid wheat genome by homologous recombination.
Since the advent of the principle of RNA guided nuclease genome editing, a number of additional tools for genome modifications and functional genomics studies have been developed . The DNA binding ability of Cas9 and Cas12 has been used to develop tools for various applications, such as transcriptional regulation and fluorescence-based imaging of specific chromosomal loci in plant genomes. Another nuclease, Cas13, has been applied to degrade mRNAs and combat viral RNA replication . Orthologues of Cas9 found in other bacterial species such as Neisseria meningitides , Staphylococcus aureus , and Campylobacter jejuni  have different and more complex Protospacer adjacent motif (PAM) sequences. These PAM sequences function in their native bacterial hosts to direct the CRISPR/Cas9 complex to the target sequence and not to the CRISPR/Cas9 locus. Although the use of these orthologous Cas9 proteins does limit the available target sequences for genome editing, it also reduces off-target edits. Most recently, systems for targeted base editing in wheat have been established by fusing a cytidine deaminase  or adenosine deaminase , to the Cas9 nickase for C/G to T/A or A/T to G/C conversion. In these systems, the efficiency of base editing was enhanced by using a Cas9-based nickase instead of an inactive Cas9. As an example, the base editor Cas9-APOBEC3A was used to edit TaMTL (MATRILINEAL) encoding a sperm-specific phospholipase . Loss of function of MTL triggers haploid induction in maize . Ten base-edited wheat mutants with TaMTL knock-out were identified at a frequency of 16.7%, with three being homozygous for all six alleles without InDels. Functional analysis of wheat mutants with TaMTL knock-out is still to be completed. Other nucleases with similar editing functions to that of Cas9 have been identified . Most notably, Cpf1 possesses both DNase and RNase activity and cleaves DNA to generate four to five bp 5′-overhangs, potentially enhancing insertion of DNA sequences by homologous recombination. The Cpf1-based editing system has been successfully applied in plants, but not in wheat at this stage [195, 196].
Although many agriculturally important traits of wheat have been targeted by genome editing, some of the main ones include the following: (i) resistance/tolerance to biotic and abiotic stresses, (ii) yield and grain quality, and (iii) male sterility.
(i) The first successful experiment using the CRISPR/Cas9 system in wheat was editing of TaMLO, a powdery mildew-resistance locus. Powdery mildew diseases caused by Blumeria graminis f. sp. tritici result in significant wheat yield losses, and knock-out of the TaMLO leads to disease resistance. The mutation frequency of TaMLO in protoplasts was 28.5% . Further, Wang et al.  described editing of the TaMLO-A1 allele by the CRISPR/Cas9 system and simultaneous editing of three homoeoalleles of TaMLO in hexaploid bread wheat using the TALEN nuclease. The mutation frequency of regenerated TaMLO-edited wheat (5.6%) was similar for both editing methods. More recently, Zhang et al.  used CRISPR/Cas9 technology to generate Taedr1 wheat lines by simultaneous knock-down of the three homologs of wheat TaEDR1, a negative regulator of powdery mildew resistance. The mutated plants were resistant to powdery mildew and did not show mildew-induced cell death .
The lipoxygenase genes, TaLpx1 and TaLox2, attracted attention as potential subjects for gene editing in relation to resistance to Fusarium, one of the most devastating fungal diseases in wheat. Lipoxygenases hydrolyze polyunsaturated fatty acids and initiate biosynthesis of oxylipins, playing a role in the activation of jasmonic acid-mediated defence responses in plants. Silencing of the TaLpx-1 gene has resulted in resistance to Fusarium graminearum in wheat . TaLpx1 and TaLox2 genes were edited in protoplasts with a mutation frequency of 9% and 45%, respectively [173, 183]. Wheat plants with mutated TaLOX2 were obtained with a frequency of 9.5%, of which homozygous mutants accounted for 44.7% .
The CRISPR/Cas9 system was also used for editing a wheat homolog of TaCer9 (ECERIFERUM9) with the goal to improve drought tolerance and water use efficiency . Mutation of the AtCer9 gene in A. thaliana, encoding an E3 ubiquitin ligase, causes elevated amounts of 18-carbon-length cutin monomers and very-long-chain free fatty acids (C24, C26) in cuticular wax, both of which are associated with elevated cuticle membrane thickness and drought tolerance .
The Cas9 nickase fused to a human cytidine deaminase, APOBEC3A, was used to produce herbicide resistant wheat plants through editing of TaALS . ALS encodes acetolactate synthase, the first enzyme of the branched-chain amino acid biosynthesis. Amino acid substitutions in TaALS confer resistance to the sulfonylurea class of herbicides. Wheat plants with a mutated TaALS gene were obtained in high frequency (22.5%, 27/120). Among them, two plants had six alleles simultaneously edited and were nicosulfuron resistant.
(ii) With the aim of enhancing grain size and yield, several genes have been edited by the CRISPR/Cas9 system: TaGASR7 [176, 184, 198], TaGW2 [198, 199, 201], and TaDEP1 . TaGASR7, a member of the Snakin/GASA gene family, has been associated with grain length in wheat. A CRISPR/Cas9 vector designed to target TaGASR7 was delivered by particle bombardment into shoot apical meristems. Eleven (5.2%) of the 210 bombarded plants carried mutant alleles, and the mutations of three (1.4%) of these were inherited in the next generation . Transiently expressing the CRISPR/Cas9 DNA and using the CRISPR/Cas9 RNP-mediated method were also highly effective for TaGASR7 editing [176, 198]. The TaGW2 gene encodes a previously unknown RING-type E3 ubiquitin ligase that was reported to be a negative regulator of grain size and thousand grain weight in wheat [198, 199, 201]. Recent studies detailing the functionality of the allelic TaGW2 genes through genome-specific knockouts , showed that the TaGW2 gene in wheat acts by regulating the gibberellin hormone biosynthesis pathway , principally confirming the parallel functions of these genes in rice and wheat. T1 plants carrying knock-out mutations in all three copies of the TaGW2 gene (genotype aabbdd) showed significantly increased thousand grain weight (27.7%), grain area (17.0%), grain width (10.9%), and grain length (6.1%) compared to the wild-type cultivar .
Another gene editing target is DENSE AND ERECT PANICLE 1 (DEP1), which encodes a G protein gamma-subunit in rice that is involved in the regulation of erect panicles, number of grains per panicle, nitrogen uptake, and stress tolerance through the G protein signalling pathway . Zhang et al.  applied the CRISPR/Cas9 system to target TaDEP1 and TaNAC2 editing in wheat. CRISPR/Cas9-induced mutation of TaNAC2 (a member of a plant specific transcription factor family) and TaDEP1 in wheat plants was successful in 2% of cases . One possible outcome of the loss of TaNAC2 function could be increased size of grain and changes in stress responses. TaPIN1 (PINFORMED1) was edited using CRISPR/Cas9 technology with a frequency of 1% . The plant specific PIN family of efflux carriers comprises integral membrane proteins and has been associated with polar auxin transport during embryogenesis and endosperm development. It should be noted that no homozygous mutants were obtained for TaDEP1, TaNAC2, and TaPIN1 by CRISPR/Cas9 editing  probably because they were not viable.
CRISPR/Cas9 technology was also successful in obtaining low immunogenic wheat. Sánchez-León et al.  have shown that CRISPR/Cas9 technology can be used to efficiently reduce the amount of alfa-gliadins in the seeds, providing bread and durum wheat lines with reduced immunoreactivity for consumers with coeliac disease. Twenty-one mutant lines were generated (15 bread wheat and 6 durum wheat), all showing a strong reduction in α-gliadins. Up to 35 of the 45 different genes identified in the wild-type were mutated in one of the lines, and immunoreactivity, as measured by competitive ELISA assays using two monoclonal antibodies, was reduced by 85%.
(iii) Male sterility and the induction of haploids can provide a powerful tool in cultivar breeding and genetic analysis. Generation of male-sterile and doubled haploid plants can facilitate development of hybrid seed production in wheat. In maize, the male-sterile gene 45 (Ms45) encodes a strictosidine synthase-like enzyme that was shown to be required for male fertility and required for exine structuring and pollen development . Genetic analysis of mutated plants obtained by CRISPR/Cas9 technology demonstrated that all three wheat Ms45 homeologues contribute to male fertility. Mutant plants, Tams45-abd, abort pollen development resulting in male sterility.
These examples provide an insight into the many ways in which modern genome modification technologies are being used to mine the core research findings from model plant transgenesis, and finally harness that understanding to drive essential crop. The ability to enact targeted changes to the genome has revolutionized genetic modification for polyploid crop species such as wheat. There are now some enticing indications that the nearest remaining hurdle, in the form of low transformation frequencies in favoured breeding genotypes, may soon be overcome. What remains is for political entities, and the societies they represent, to adopt a more receptive view to the very real and practical benefits these technologies may provide.
6. Conclusions and Prospective Developments
Demand for wheat is projected to rise at a rate of 1.6% annually until 2050 as a result of increased population and prosperity. Consequently, average global wheat yields on a per hectare basis will need to increase to approximately 5 tonnes per ha from the current 3.3 tonnes . Bread wheat has a very complicated hexaploid genome and, therefore, further progress in breeding of this crop is strongly dependent upon knowledge of functional genomics. Thus, it is necessary to identify the most important key-genes, their structure, role, and function in the development of wheat plants and finally for higher grain yield and better quality. Based on the knowledge of functional genomics, plant biologists can alter the structures and functions of selected key-genes through “genetic manipulation”. Genetic transformation is a very powerful tool for generating scientific proof of the roles and functions of key-genes. The authors of this review are not in a position to discuss the applications of GM-wheat in world breeding practice, since this is beyond the scope of this review. However, the term “genetic manipulation” is very broad and includes other molecular approaches that generate products that fall outside the traditional definition of “GM”. RNA interference and CRISPR/Cas9 represent modern and very advanced GM technologies that in a growing number of countries, such as USA and Canada, result in products that attract the same level of regulation as the products of traditional breeding techniques. Such “end-product-based” rather than “process-based” regulation, presents a far more favourable environment for the progression of molecular-based breeding technologies, which can and should change the future of wheat breeding across the world. However, all advanced methods will remain simply “laboratory tools” if their application is not connected with wheat breeders currently working by traditional methods. Therefore, we see the chance for real progress and positive future prospects through effective collaborations between plant molecular geneticists and wheat breeders. The application of novel methods and analysis of genetically manipulated wheat plants for their utility in breeding can be translated to the field through the introgression of genetic traits into conventional wheat breeding programs.
Awareness and concerns are also growing regarding the huge economic gaps between developed and developing countries. Underdeveloped countries are more reliant on agriculture for their overall economies, yet they have fewer opportunities to develop or collaborate on projects involving modern technologies for genetic manipulation in wheat and most other crop plants. Therefore, researchers in developed countries must take the lead and assume responsibility for sharing and freely disseminating their results and genetically manipulated wheat germplasm accessions with breeders in the developing world. This act of “research donation” can enrich lives and communities where needs are the greatest and uphold the future security and sustainability of wheat production, a key global commodity.
Conflicts of Interest
The authors declare that the research was conducted in the absence of any potential conflicts of interest.
We want to thank the staff and students of Huaiyin Normal University, Huaian, China, Flinders University of South Australia, SA, Australia, and S. Seifullin Kazakh AgroTechnical University, Astana, Kazakhstan, for their support in this research and help with critical comments to the manuscript. This research was supported by a personal grant to NB from the Huaiyin Normal University, Huaian, China. The Ministry of Education and Science (Kazakhstan) also provided financial support for this research through Research Program BR05236500 (SJ).
- C. Uauy, “Plant genomics: unlocking the genome of wheat’s progenitor,” Current Biology, vol. 27, no. 20, pp. R1122–R1124, 2017.
- R. E. Evenson and D. Gollin, “Assessing the impact of the green revolution, 1960 to 2000,” Science, vol. 300, no. 5620, pp. 758–762, 2003.
- P. Langridge, “Wheat genomics and the ambitious targets for future wheat production,” Genome, vol. 56, no. 10, pp. 545–547, 2013.
- R. J. Henry, P. Rangan, and A. Furtado, “Functional cereals for production in new and variable climates,” Current Opinion in Plant Biology, vol. 30, pp. 11–18, 2016.
- F. Altpeter, N. M. Springer, L. E. Bartley et al., “Advancing crop transformation in the era of genome editing,” The Plant Cell, vol. 28, pp. 1510–1520, 2016.
- F. Altpeter, N. Baisakh, R. Beachy et al., “Particle bombardment and the genetic enhancement of crops: myths and realities,” Molecular Breeding, vol. 15, no. 3, pp. 305–327, 2005.
- H. Wu, F. S. Awan, A. Vilarinho et al., “Transgene integration complexity and expression stability following biolistic or agrobacterium-mediated transformation of sugarcane,” In Vitro Cellular & Developmental Biology - Plant, vol. 51, no. 6, pp. 603–611, 2015.
- Y. Ishida, M. Tsunashima, Y. Hiei, and T. Komari, “Wheat (triticum aestivum L.) transformation using immature embryos,” in Agrobacterium Protocols, vol. 1223 of Methods in Molecular Biology, pp. 189–198, Springer New York, New York, NY, USA, 2015.
- A. Pellegrineschi, L. M. Noguera, B. Skovmand et al., “Identification of highly transformable wheat genotypes for mass production of fertile transgenic plants,” Genome, vol. 45, no. 2, pp. 421–430, 2002.
- C. Tassy and P. Barret, “Biolistic transformation of wheat,” in Wheat Biotechnology: Methods and Protocols, P. Bhalla and M. Singh, Eds., vol. 1679 of Methods in Molecular Biology, pp. 141–152, Springer New York, New York, NY, 2017.
- H. D. Jones, A. Doherty, and C. A. Sparks, “Transient transformation of plants,” in Plant Genomics, J. M. Walker, Ed., vol. 513 of Methods in Molecular Biology, pp. 131–152, Humana Press, Totowa, NJ, USA, 2009.
- A. C. Brasileiro, C. Tourneur, J. Leple, V. Combes, and L. Jouanin, “Expression of the mutant arabidopsis thaliana acetolactate synthase gene confers chlorsulfuron resistance to transgenic poplar plants,” Transgenic Research, vol. 1, no. 3, pp. 133–141, 1992.
- J. Mullen, G. Adam, A. Blowers, and E. Earle, “Biolistic transfer of large DNA fragments to tobacco cells using YACs retro fitted for plant transformation,” Molecular Breeding, vol. 4, no. 5, pp. 449–457, 1998.
- Y. Wang, H. Zeng, X. Zhou et al., “Transformation of rice with large maize genomic DNA fragments containing high content repetitive sequences,” Plant Cell Reports, vol. 34, no. 6, pp. 1049–1061, 2015.
- S. De Buck, C. De Wilde, M. Van Montagu, and A. Depicker, “T-DNA vector backbone sequences are frequently integrated into the genome of transgenic plants obtained by Agrobacterium-mediated transformation,” Molecular Breeding, vol. 6, pp. 459–468, 2000.
- B. Ülker, Y. Li, M. G. Rosso, E. Logemann, I. E. Somssich, and B. Weisshaar, “T-DNA-mediated transfer of Agrobacterium tumefaciens chromosomal DNA into plants,” Nature Biotechnology, vol. 26, no. 9, pp. 1015–1017, 2008.
- A. Gadaleta, A. Giancaspro, A. Blechl, and A. Blanco, “Phosphomannose isomerase, pmi, as a selectable marker gene for durum wheat transformation,” Journal of Cereal Science, vol. 43, pp. 31–37, 2006.
- A. Gadaleta, A. Giancaspro, A. E. Blechl, and A. Blanco, “A transgenic durum wheat line that is free of marker genes and expresses 1Dy10,” Journal of Cereal Science, vol. 48, no. 2, pp. 439–445, 2008.
- K. Wang, H. Liu, L. Du, and X. Ye, “Generation of marker-free transgenic hexaploid wheat via an agrobacterium-mediated co-transformation strategy in commercial Chinese wheat varieties,” Plant Biotechnology Journal, vol. 15, no. 5, pp. 614–623, 2017.
- T. Risacher, M. Craze, S. Bowden, W. Paul, and T. Barsby, “Highly efficient agrobacterium-mediated transformation of wheat via in planta inoculation,” Methods in Molecular Biology, vol. 478, pp. 115–124, 2009.
- J. M. Zale, S. Agarwal, S. Loar, and C. M. Steber, “Evidence for stable transformation of wheat by floral dip in agrobacterium tumefaciens,” Plant Cell Reports, vol. 28, no. 6, pp. 903–913, 2009.
- H. Hamada, Q. Linghu, Y. Nagira, R. Miki, N. Taoka, and R. Imai, “An in planta biolistic method for stable wheat transformation,” Scientific Reports, vol. 7, article 11443, 2017.
- S. Martin-Ortigosa and K. Wang, “Proteolistics: a biolistic method for intracellular delivery of proteins,” Transgenic Research, vol. 23, no. 5, pp. 743–756, 2014.
- C. Remacle, P. Cardol, N. Coosemans, M. Gaisne, and N. Bonnefoy, “High-efficiency biolistic transformation of Chlamydomonas mitochondria can be used to insert mutations in complex I genes,” Proceedings of the National Acadamy of Sciences of the United States of America, vol. 103, no. 12, pp. 4771–4776, 2006.
- L. Cheng, H. Li, B. Qu et al., “Chloroplast transformation of rapeseed (Brassica napus) by particle bombardment of cotyledons,” Plant Cell Reports, vol. 29, no. 4, pp. 371–381, 2010.
- Y. Gleba, V. Klimyuk, and S. Marillonnet, “Magnifection - a new platform for expressing recombinant vaccines in plants,” Vaccine, vol. 23, no. 17-18, pp. 2042–2048, 2005.
- S. Ueki, S. Magori, B. Lacroix, and V. Citovsky, “Transient gene expression in epidermal cells of plant leaves by biolistic DNA delivery,” in Biolistic DNA Delivery: Methods and Protocols, Methods in Molecular Biology, S. Sudowe and A. B. Reske-Kunz, Eds., vol. 940, pp. 17–26, 2013.
- P. Krenek, O. Samajova, I. Luptovciak, A. Doskocilova, G. Komis, and J. Samaj, “Transient plant transformation mediated by Agrobacterium tumefaciens: Principles, methods and applications,” Biotechnology Advances, vol. 33, no. 6, pp. 1024–1042, 2015.
- N. Goncharov and E. Kondratenkо, “Origin, domestication and evolution of wheats,” Vestnik VOGiS, vol. 12, pp. 159–179, 2008, http://www.bionet.nsc.ru/vogis/pict_pdf/2008/t12_1_2/vogis_12_1_2_15.pdf.
- J. D. Montenegro, A. A. Golicz, P. E. Bayer et al., “The pangenome of hexaploid bread wheat,” The Plant Journal, vol. 90, no. 5, pp. 1007–1013, 2017.
- P. L. Bhalla, A. Sharma, and M. B. Singh, “Enabling molecular technologies for trait improvement in wheat,” in Wheat Biotechnology, vol. 1679 of Methods in Molecular Biology, pp. 3–24, Springer New York, New York, NY, USA, 2017.
- R. Appels, K. Eversole, C. Feuillet et al., “Shifting the limits in wheat research and breeding using a fully annotated reference genome,” Science, vol. 361, no. 6403, article eaar7191, 2018.
- A. K. Shrawat and C. L. Armstrong, “Development and application of genetic engineering for wheat improvement,” Critical Reviews in Plant Sciences, vol. 37, no. 5, pp. 335–421, 2018.
- V. Vasil, A. M. Castillo, M. E. Fromm, and I. K. Vasil, “Herbicide resistant fertile transgenic wheat plants obtained by microprojectile bombardment of regenerable embryogenic callus,” Nature Biotechnology, vol. 10, no. 6, pp. 667–674, 1992.
- M. Cheng, J. E. Fry, S. Pang et al., “Genetic transformation of wheat mediated by agrobacterium tumefaciens,” Plant Physiology, vol. 115, no. 3, pp. 971–980, 1997.
- Q. Yao, L. Cong, J. L. Chang, K. X. Li, G. X. Yang, and G. Y. He, “Low copy number gene transfer and stable expression in a commercial wheat cultivar via particle bombardment,” Journal of Experimental Botany, vol. 57, no. 14, pp. 3737–3746, 2006.
- C. Tassy, A. Partier, M. Beckert, C. Feuillet, and P. Barret, “Biolistic transformation of wheat: increased production of plants with simple insertions and heritable transgene expression,” Plant Cell, Tissue and Organ Culture (PCTOC), vol. 119, no. 1, pp. 171–181, 2014.
- A. Ismagul, N. Yang, E. Maltseva et al., “A biolistic method for high-throughput production of transgenic wheat plants with single gene insertions,” BMC Plant Biology, vol. 18, pp. 135–143, 2018.
- Q. Yao, L. Cong, G. He et al., “Optimization of wheat co-transformation procedure with gene cassettes resulted in an improvement in transformation frequency,” Molecular Biology Reports, vol. 34, pp. 61–67, 2007.
- A. Partier, G. Gay, C. Tassy, M. Beckert, C. Feuillet, and P. Barret, “Molecular and FISH analyses of a 53-kbp intact DNA fragment inserted by biolistics in wheat (triticum aestivum L.) genome,” Plant Cell Reports, vol. 36, no. 10, pp. 1547–1559, 2017.
- M. Wright, J. Dawson, E. Dunder et al., “Efficient biolistic transformation of maize (Zea mays L.) and wheat (Triticum aestivum L.) using the phosphomannose isomerase gene, pmi, as the selectable marker,” Plant Cell Reports, vol. 20, no. 5, pp. 429–436, 2001.
- T. Richardson, J. Thistleton, T. J. Higgins, C. Howitt, and M. Ayliffe, “Efficient agrobacterium transformation of elite wheat germplasm without selection,” Plant Cell, Tissue and Organ Culture (PCTOC), vol. 119, no. 3, pp. 647–659, 2014.
- G. Hensel, C. Marthe, and J. Kumlehn, “Agrobacterium-mediated transformation of wheat using immature embryos,” in Wheat Biotechnology, P. Bhalla and M. Singh, Eds., vol. 1679 of Methods in Molecular Biology, pp. 129–139, Springer New York, New York, NY, USA, 2017.
- K. Wang, B. Riaz, and X. Ye, “Wheat genome editing expedited by efficient transformation techniques: progress and perspectives,” The Crop Journal, vol. 6, no. 1, pp. 22–31, 2018.
- G. R. Lazo, P. A. Stein, and R. A. Ludwig, “A DNA transformation-competent Arabidopsis genomic library in agrobacterium,” Nature Biotechnology, vol. 9, no. 10, pp. 963–967, 1991.
- N. R. Peters, S. Ackerman, and E. A. Davis, “A modular vector for Agrobacterium mediated transformation of wheat,” Plant Molecular Biology Reporter, vol. 17, no. 4, pp. 323–331, 1999.
- N. V. Larebeke, G. Engler, M. Holsters et al., “Large plasmid in agrobacterium tumefaciens essential for crown gall-inducing ability,” Nature, vol. 252, no. 5479, pp. 169-170, 1974.
- Y. Wang, M. Xu, G. Yin, L. Tao, D. Wang, and X. Ye, “Transgenic wheat plants derived from Agrobacterium-mediated transformation of mature embryo tissues,” Cereal Research Communications, vol. 37, pp. 1–12, 2009.
- P. Supartana, T. Shimizu, M. Nogawa et al., “Development of simple and efficient in planta transformation method for wheat (triticum aestivum l.) using agrobacterium tumefaciens,” Journal of Bioscience and Bioengineering, vol. 102, no. 3, pp. 162–170, 2006.
- H. Aadel, R. Abdelwahd, S. Udupa et al., “Agrobacterium-mediated transformation of mature embryo tissues of bread wheat (triticum aestivum L.) genotypes,” Cereal Research Communications, vol. 46, pp. 10–20, 2018.
- E. Medvecká and W. A. Harwood, “Wheat (triticum aestivum L.) transformation using mature embryos,” in Agrobacterium Protocols: Volume 1, K. Wang, Ed., vol. 1223 of Methods in Molecular Biology, pp. 199–209, Springer New York, New York, NY, USA, 2015.
- H. Chauhan and P. Khurana, “Wheat genetic transformation using mature embryos as explants,” in Wheat Biotechnology: Methods and Protocols, P. Bhalla and M. Singh, Eds., vol. 1679 of Methods in Molecular Biology, pp. 153–167, Humana Press, New York, NY, USA, 2017.
- T. Zhao, S. Zhao, H. Chen et al., “Transgenic wheat progeny resistant to powdery mildew generated by agrobacterium inoculum to the basal portion of wheat seedling,” Plant Cell Reports, vol. 25, no. 11, pp. 1199–1204, 2006.
- A. Razzaq, I. A. Hafiz, I. Mahmood, and A. Hussain, “Development of in planta transformation protocol for wheat,” African Journal of Biotechnology, vol. 10, no. 5, pp. 740–750, 2011.
- S. Rustgi, N. O. Ankrah, R. A. T. Brew-Appiah et al., “Doubled haploid transgenic wheat lines by microspore transformation,” in Wheat Biotechnology: Methods and Protocols, P. Bhalla and M. Singh, Eds., vol. 1679 of Methods in Molecular Biology, pp. 213–234, Humana Press, New York, NY, USA, 2017.
- L. Folling and A. Olesen, “Transformation of wheat (triticum aestivum L.) microspore-derived callus and microspores by particle bombardment,” Plant Cell Reports, vol. 20, no. 7, pp. 629–636, 2001.
- R. A. Brew-Appiah, N. Ankrah, W. Liu et al., “Generation of doubled haploid transgenic wheat lines by microspore transformation,” PLoS ONE, vol. 8, no. 11, article e80155, 2013.
- K. Singer, Y. M. Shiboleth, J. Li, and T. Tzfira, “Formation of complex extrachromosomal T-DNA structures in agrobacterium tumefaciens-infected plants,” Plant Physiology, vol. 160, pp. 511–522, 2012.
- S. Kim and G. An, “Bacterial transposons are co-transferred with T-DNA to rice chromosomes during Agrobacterium-mediated transformation,” Molecules and Cells, vol. 33, no. 6, pp. 583–589, 2012.
- A. Pitzschke, “Agrobacterium infection and plant defense-transformation success hangs by a thread,” Frontiers in Plant Science, vol. 4, no. 519, 2013.
- E. Zuniga-Soto, E. Mullins, and B. Dedicova, “Ensifer-mediated transformation: an efficient non-agrobacterium protocol for the genetic modification of rice,” SpringerPlus, vol. 4, pp. 1–10, 2015.
- M. S. Greer, I. Kovalchuk, and F. Eudes, “Ammonium nitrate improves direct somatic embryogenesis and biolistic transformation of Triticum aestivum,” New Biotechnology, vol. 26, no. 1-2, pp. 44–52, 2009.
- Y. Dan, “Biological functions of antioxidants in plant transformation,” In Vitro Cellular & Developmental Biology - Plant, vol. 44, no. 3, pp. 149–161, 2008.
- Y. Dan, C. L. Armstrong, J. Dong et al., “Lipoic acid—an unique plant transformation enhancer,” In Vitro Cellular & Developmental Biology - Plant, vol. 45, no. 6, pp. 630–638, 2009.
- Y. Coskun, R. E. Duran, C. Savaskan, T. Demirci, and M. T. Hakan, “Efficient plant regeneration with arabinogalactan-proteins on various ploidy levels of cereals,” Journal of Integrative Agriculture, vol. 12, no. 3, pp. 420–425, 2013.
- R. Kumar, H. M. Mamrutha, A. Kaur et al., “Development of an efficient and reproducible regeneration system in wheat (triticum aestivum L.),” Physiology and Molecular Biology of Plants, vol. 23, no. 4, pp. 945–954, 2017.
- D. Miroshnichenko, I. Chaban, M. Chernobrovkina, S. Dolgov, and R. P. Niedz, “Protocol for efficient regulation of in vitro morphogenesis in einkorn (triticum monococcum L.), a recalcitrant diploid wheat species,” PLoS ONE, vol. 12, no. 3, Article ID e0173533, 2017.
- R. A. Jefferson, “Assaying chimeric genes in plants: the GUS gene fusion system,” Plant Molecular Biology Reporter, vol. 5, no. 4, pp. 387–405, 1987.
- M. Hraška, S. Rakouský, and V. Čurn, “Green fluorescent protein as a vital marker for non-destructive detection of transformation events in transgenic plants,” Plant Cell, Tissue and Organ Culture, vol. 86, no. 3, pp. 303–318, 2006.
- J. Zhang, D. Yu, Y. Zhang et al., “Vacuum and co-cultivation agroinfiltration of (Germinated) seeds results in tobacco rattle virus (TRV) mediated whole-plant virus-induced gene silencing (VIGS) in wheat and maize,” Frontiers in Plant Science, vol. 8, no. 393, 2017.
- S. Naqvi, G. Farré, G. Sanahuja, T. Capell, C. Zhu, and P. Christou, “When more is better: multigene engineering in plants,” Trends in Plant Science, vol. 15, no. 1, pp. 48–56, 2010.
- W. Yu, Y. Yau, and J. A. Birchler, “Plant artificial chromosome technology and its potential application in genetic engineering,” Plant Biotechnology Journal, vol. 14, no. 5, pp. 1175–1182, 2016.
- J. Yuan, Q. Shi, X. Guo et al., “Site-specific transfer of chromosomal segments and genes in wheat engineered chromosomes,” Journal of Genetics and Genomics, vol. 44, no. 11, pp. 531–539, 2017.
- A. Furtado, R. J. Henry, and A. Pellegrineschi, “Analysis of promoters in transgenic barley and wheat,” Plant Biotechnology Journal, vol. 7, no. 3, pp. 240–253, 2009.
- S. Alotaibi, C. Sparks, M. Parry, A. Simkin, and C. Raines, “Identification of leaf promoters for use in transgenic wheat,” Plants, vol. 7, no. 2, p. E27, 2018.
- G. Hensel, A. Himmelbach, W. Chen, D. K. Douchkov, and J. Kumlehn, “Transgene expression systems in the triticeae cereals,” Journal of Plant Physiology, vol. 168, pp. 30–44, 2011.
- N. Borisjuk, M. Hrmova, and S. Lopato, “Transcriptional regulation of cuticle biosynthesis,” Biotechnology Advances, vol. 32, no. 2, pp. 526–540, 2014.
- H. Wang, H. Wang, H. Shao, and X. Tang, “Recent advances in utilizing transcription factors to improve plant abiotic stress tolerance by transgenic technology,” Frontiers in Plant Science, vol. 7, no. 67, 2016.
- H. Bi, J. Shi, N. Kovalchuk et al., “Overexpression of the TaSHN1 transcription factor in bread wheat leads to leaf surface modifications, improved drought tolerance, and no yield penalty under controlled growth conditions,” Plant, Cell & Environment, vol. 41, no. 11, pp. 2549–2566, 2018.
- R. P. Singh, P. K. Singh, J. Rutkoski et al., “Disease impact on wheat yield potential and prospects of genetic control,” Annual Review of Phytopathology, vol. 54, pp. 303–322, 2016.
- A. E. Ricroch, “What will be the benefits of biotech wheat for european agriculture?” Methods of Molecular Biology, vol. 1679, pp. 25–35, 2017.
- B. Keller, T. Wicker, and S. G. Krattinger, “Advances in wheat and pathogen genomics: implications for disease control,” Annual Review of Phytopathology, vol. 56, pp. 67–87, 2018.
- H. Budak, B. Hussain, Z. Khan, N. Z. Ozturk, and N. Ullah, “From genetics to functional genomics: improvement in drought signaling and tolerance in wheat,” Frontiers in Plant Science, vol. 19, no. 1012, 2015.
- S. Khan, M. Li, S. Wang, and H. Yin, “Revisiting the role of plant transcription factors in the battle against abiotic stress,” International Journal of Molecular Sciences, vol. 19, no. 6, p. E1634, 2018.
- Y. Yu, D. Zhu, C. Ma et al., “Transcriptome analysis reveals key differentially expressed genes involved in wheat grain development,” The Crop Journal, vol. 4, no. 2, pp. 92–106, 2016.
- A. Nadolska-Orczyk, I. K. Rajchel, W. Orczyk, and S. Gasparis, “Major genes determining yield-related traits in wheat and barley,” Theoretical and Applied Genetics, vol. 130, no. 6, pp. 1081–1098, 2017.
- R. J. Henry, A. Furtado, and P. Rangan, “Wheat seed transcriptome reveals genes controlling key traits for human preference and crop adaptation,” Current Opinion in Plant Biology, vol. 45, pp. 231–236, 2018.
- V. C. Gegas, A. Nazari, S. Griffiths et al., “A genetic framework for grain size and shape variation in wheat,” The Plant Cell, vol. 22, no. 4, pp. 1046–1056, 2010.
- Z. Su, C. Hao, L. Wang, Y. Dong, and X. Zhang, “Identification and development of a functional marker of TaGW2 associated with grain weight in bread wheat (triticum aestivum L.),” Theoretical and Applied Genetics, vol. 122, pp. 211–223, 2011.
- X. Song, W. Huang, M. Shi, M. Zhu, and H. Lin, “A QTL for rice grain width and weight encodes a previously unknown RING-type E3 ubiquitin ligase,” Nature Genetics, vol. 39, no. 5, pp. 623–630, 2007.
- J. Bednarek, A. Boulaflous, C. Girousse et al., “Down-regulation of the TaGW2 gene by RNA interference results in decreased grain size and weight in wheat,” Journal of Experimental Botany, vol. 63, no. 16, pp. 5945–5955, 2012.
- Y. Hong, L. Chen, L. Du et al., “Transcript suppression of TaGW2 increased grain width and weight in bread wheat,” Functional & Integrative Genomics, vol. 14, no. 2, pp. 341–349, 2014.
- W. Zalewski, W. Orczyk, S. Gasparis, and A. Nadolska-Orczyk, “HvCKX2 gene silencing by biolistic or Agrobacterium-mediated transformation in barley leads to different phenotypes,” BMC Plant Biology, vol. 12, no. 206, 2012.
- P. J. Andralojc, E. Carmo-Silva, G. E. Degen, and M. A. J. Parry, “Increasing metabolic potential: C-fixation,” Essays in Biochemistry, vol. 62, pp. 109–118, 2018.
- A. Prins, D. J. Orr, P. J. Andralojc, M. P. Reynolds, E. Carmo-Silva, and M. A. Parry, “Rubisco catalytic properties of wild and domesticated relatives provide scope for improving wheat photosynthesis,” Journal of Experimental Botany, vol. 67, no. 6, pp. 1827–1838, 2016.
- M. T. Lin, A. Occhialini, P. J. Andralojc, M. A. Parry, and M. R. Hanson, “A faster Rubisco with potential to increase photosynthesis in crops,” Nature, vol. 513, no. 7519, pp. 547–550, 2014.
- E. Carmo-Silva, J. C. Scales, P. J. Madgwick, and M. A. Parry, “Optimizing Rubisco and its regulation for greater resource use efficiency,” Plant, Cell & Environment, vol. 38, no. 9, pp. 1817–1832, 2015.
- R. A. Richards, “Selectable traits to increase crop photosynthesis and yield of grain crops,” Journal of Experimental Botany, vol. 51, pp. 447–458, 2000.
- Y. Taniguchi, H. Ohkawa, C. Masumoto et al., “Overproduction of C4 photosynthetic enzymes in transgenic rice plants: an approach to introduce the C4-like photosynthetic pathway into rice,” Journal of Experimental Botany, vol. 59, no. 7, pp. 1799–1809, 2007.
- L. Hu, Y. Li, W. Xu et al., “Improvement of the photosynthetic characteristics of transgenic wheat plants by transformation with the maize C4 phosphoenolpyruvate carboxylase gene,” Plant Breeding, vol. 131, no. 3, pp. 385–391, 2012.
- H. Zhang, W. Xu, H. Wang et al., “Pyramiding expression of maize genes encoding phosphoenolpyruvate carboxylase (PEPC) and pyruvate orthophosphate dikinase (PPDK) synergistically improve the photosynthetic characteristics of transgenic wheat,” Protoplasma, vol. 251, no. 5, pp. 1163–1173, 2014.
- N. Qin, W. Xu, L. Hu et al., “Drought tolerance and proteomics studies of transgenic wheat containing the maize C4 phosphoenolpyruvate carboxylase (PEPC) gene,” Protoplasma, vol. 253, no. 6, pp. 1503–1512, 2016.
- P. A. Peña, T. Quach, S. Sato et al., “Expression of the maize Dof1 transcription factor in wheat and sorghum,” Frontiers in Plant Science, vol. 8, no. 434, 2017.
- Z. A. Myers and B. F. Holt III., “Nuclear factor-Y: still complex after all these years?” Current Opinion in Plant Biology, vol. 45, pp. 96–102, 2018.
- M. E. Zanetti, C. Rípodas, and A. Niebel, “Plant NF-Y transcription factors: key players in plant-microbe interactions, root development and adaptation to stress,” Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms, vol. 1860, no. 5, pp. 645–654, 2017.
- B. Qu, X. He, J. Wang et al., “A wheat CCAAT box-binding transcription factor increases the grain yield of wheat with less fertilizer input,” Plant Physiology, vol. 167, no. 2, pp. 411–423, 2015.
- D. Yadav, Y. Shavrukov, N. Bazanova et al., “Constitutive overexpression of the TaNF-YB4 gene in transgenic wheat significantly improves grain yield,” Journal of Experimental Botany, vol. 66, no. 21, pp. 6635–6650, 2015.
- X. He, B. Qu, W. Li et al., “The nitrate-inducible NAC transcription factor TaNAC2-5A controls nitrate response and increases wheat yield,” Plant Physiology, vol. 169, pp. 1991–2005, 2015.
- B. Tian, S. K. Talukder, J. Fu, A. K. Fritz, and H. N. Trick, “Expression of a rice soluble starch synthase gene in transgenic wheat improves the grain yield under heat stress conditions,” In Vitro Cellular & Developmental Biology - Plant, vol. 54, no. 3, pp. 216–227, 2018.
- M. Hu, X. Zhao, Q. Liu et al., “Transgenic expression of plastidic glutamine synthetase increases nitrogen uptake and yield in wheat,” Plant Biotechnology Journal, vol. 16, no. 11, pp. 1858–1867, 2018.
- X. Zhu, S. P. Long, and D. R. Ort, “What is the maximum efficiency with which photosynthesis can convert solar energy into biomass?” Current Opinion in Biotechnology, vol. 19, no. 2, pp. 153–159, 2008.
- U. Sonnewald and J. Kossmann, “Starches-from current models to genetic engineering,” Plant Biotechnology Journal, vol. 11, no. 2, pp. 223–232, 2013.
- R. Kumar, S. Mukherjee, and B. T. Ayele, “Molecular aspects of sucrose transport and its metabolism to starch during seed development in wheat: a comprehensive review,” Biotechnology Advances, vol. 36, no. 4, pp. 954–967, 2018.
- N. Weichert, I. Saalbach, H. Weichert et al., “Increasing sucrose uptake capacity of wheat grains stimulates storage protein synthesis,” Plant Physiology, vol. 152, no. 2, pp. 698–710, 2010.
- E. D. Smidansky, F. D. Meyer, B. Blakeslee, T. E. Weglarz, T. W. Greene, and M. J. Giroux, “Expression of a modified ADP-glucose pyrophosphorylase large subunit in wheat seeds stimulates photosynthesis and carbon metabolism,” Planta, vol. 225, no. 4, pp. 965–976, 2007.
- G. Kang, W. Xu, G. Liu, X. Peng, T. Guo, and J. Bell, “Comprehensive analysis of the transcription of starch synthesis genes and the transcription factor RSR1 in wheat (triticum aestivum) endosperm,” Genome, vol. 56, no. 2, pp. 115–122, 2013.
- G. Liu, Y. Wu, M. Xu et al., “Virus-Induced gene silencing identifies an important role of the TaRSR1 transcription factor in starch synthesis in bread wheat,” International Journal of Molecular Sciences, vol. 17, no. 10, p. 1557, 2016.
- M. Meenu and B. Xu, “A critical review on anti-diabetic and anti-obesity effects of dietary resistant starch,” Critical Reviews in Food Science and Nutrition, pp. 1–13, 2018.
- A. Regina, A. Bird, D. Topping et al., “High-amylose wheat generated by RNA interference improves indices of large-bowel health in rats,” Proceedings of the National Acadamy of Sciences of the United States of America, vol. 103, no. 10, pp. 3546–3551, 2006.
- F. Sestili, M. Janni, A. Doherty et al., “Increasing the amylose content of durum wheat through silencing of the SBEIIa genes,” BMC Plant Biology, vol. 10, no. 144, 2010.
- C. Vetrani, F. Sestili, M. Vitale et al., “Metabolic response to amylose-rich wheat-based rusks in overweight individuals,” European Journal of Clinical Nutrition, vol. 72, no. 6, pp. 904–912, 2018.
- C. Zörb, U. Ludewig, and M. J. Hawkesford, “Perspective on wheat yield and quality with reduced nitrogen supply,” Trends in Plant Science, vol. 23, no. 11, pp. 1029–1037, 2018.
- D. Zhao, A. P. Derkx, D. Liu, P. Buchner, M. J. Hawkesford, and E. Flemetakis, “Overexpression of a NAC transcription factor delays leaf senescence and increases grain nitrogen concentration in wheat,” The Journal of Plant Biology, vol. 17, no. 4, pp. 904–913, 2015.
- X. Zhao, X. Nie, X. Xiao, and H. Yang, “Over-expression of a tobacco nitrate reductase gene in wheat (triticum aestivum l.) increases seed protein content and weight without augmenting nitrogen supplying,” PLoS ONE, vol. 8, no. 9, article e74678, 2013.
- F. M. Anjum, M. R. Khan, A. Din, M. Saeed, I. Pasha, and M. U. Arshad, “Wheat gluten: high molecular weight glutenin subunits?structure, genetics, and relation to dough elasticity,” Journal of Food Science, vol. 72, no. 3, pp. R56–R63, 2007.
- F. Altpeter, V. Vasil, V. Srivastava, and I. K. Vasil, “Integration and expression of the high-molecular-weight glutenin subunit 1Ax1 gene into wheat,” Nature Biotechnology, vol. 14, no. 9, pp. 1155–1159, 1996.
- A. E. Blechl and O. D. Anderson, “Expression of a novel high-molecular-weight glutenin subunit gene in transgenic wheat,” Nature Biotechnology, vol. 14, no. 7, pp. 875–879, 1996.
- F. Barro, L. Rooke, F. Békés et al., “Transformation of wheat with high molecular weight subunit genes results in improved functional properties,” Nature Biotechnology, vol. 15, no. 12, pp. 1295–1299, 1997.
- L. Rooke, F. Békés, R. Fido et al., “Overexpression of a gluten protein in transgenic wheat results in greatly increased dough strength,” Journal of Cereal Science, vol. 30, no. 2, pp. 115–120, 1999.
- M. L. Alvarez, M. Gómez, J. María Carrillo, and R. H. Vallejos, “Analysis of dough functionality of flours from transgenic wheat,” Molecular Breeding, vol. 8, pp. 103–108, 2001.
- P. R. Shewry, S. Powers, J. M. Field et al., “Comparative field performance over 3 years and two sites of transgenic wheat lines expressing HMW subunit transgenes,” Theoretical and Applied Genetics, vol. 113, pp. 128–136, 2006.
- Y. Li, Q. Wang, X. Li et al., “Coexpression of the high molecular weight glutenin subunit 1ax1 and puroindoline improves dough mixing properties in durum wheat (triticum turgidum l. ssp. durum),” PLoS ONE, vol. 7, no. 11, article e50057, 2012.
- S. Li, N. Wang, Y. Wang et al., “Inheritance and expression of copies of transgenes 1Dx5 and 1Ax1 in elite wheat (triticum aestivum l.) varieties transferred from transgenic wheat through conventional crossing,” Acta Biochimica et Biophysica Sinica, vol. 39, no. 5, pp. 377–383, 2007.
- X. Mao, Y. Li, S. Zhao et al., “The interactive effects of transgenically overexpressed 1Ax1 with various HMW-GS combinations on dough quality by introgression of exogenous subunits into an elite chinese wheat variety,” PLoS ONE, vol. 8, no. 10, article e78451, 2013.
- P. I. Payne, “Genetics of wheat storage proteins and the effect of allelic variation on bread-making quality,” Annual Review of Plant Physiology and Plant Molecular Biology, vol. 38, pp. 141–153, 1987.
- K. A. Scherf, P. Koehler, and H. Wieser, “Gluten and wheat sensitivities – an overview,” Journal of Cereal Science, vol. 67, pp. 2–11, 2016.
- A. Juhász, T. Belova, C. G. Florides et al., “Genome mapping of seed-borne allergens and immunoresponsive proteins in wheat,” Science Advances, vol. 4, no. 8, article eaar8602, 2018.
- I. Cakmak, H. Ozkan, H. J. Braun, R. M. Welch, and V. Romheld, “Zinc and iron concentrations in seeds of wild, primitive, and modern wheats,” Food and Nutrition Bulletin, vol. 21, no. 4, pp. 401–403, 2000.
- R. M. Welch and R. D. Graham, “A new paradigm for world agriculture: meeting human needs. productive, sustainable, nutritious,” Field Crops Research, vol. 60, no. 1-2, pp. 1–10, 1999.
- P. B. Holm, K. N. Kristiansen, and H. B. Pedersen, “Transgenic approaches in commonly consumed cereals to improve iron and zinc content and bioavailability,” Journal of Nutrition, vol. 132, no. 3, pp. 514S–516S, 2002.
- S. Borg, H. Brinch-Pedersen, B. Tauris et al., “Wheat ferritins: improving the iron content of the wheat grain,” Journal of Cereal Science, vol. 56, no. 2, pp. 204–213, 2012.
- X. Sui, Y. Zhao, S. Wang et al., “Improvement Fe content of wheat (triticum aestivum) grain by soybean ferritin expression cassette without vector backbone sequence,” Journal of Agricultural Biotechnology, vol. 20, pp. 766–773, 2012.
- J. M. Connorton, E. R. Jones, I. Rodríguez-Ramiro et al., “Wheat vacuolar iron transporter TaVIT2 transports Fe and Mn and is effective for biofortification,” Plant Physiology, vol. 174, pp. 2434–2444, 2017.
- L. Yan, A. Loukoianov, A. Blechl et al., “The wheat VRN2 gene is a flowering repressor down-regulated by vernalization,” Science, vol. 303, no. 5664, pp. 1640–1644, 2004.
- A. Loukoianov, L. Yan, and A. Blechl, “Regulation of VRN-1 vernalization genes in normal and transgenic polyploid wheat,” Plant Physiology, vol. 138, no. 4, pp. 2364–2373, 2005.
- C. Uauy, A. Distelfeld, T. Fahima, A. Blechl, and J. Dubcovsky, “A NAC gene regulating senescence improves grain protein, Zinc, and iron content in wheat,” Science, vol. 314, no. 5803, pp. 1298–1301, 2006.
- Y. Li, G. Song, J. Gao et al., “Enhancement of grain number per spike by RNA interference of cytokinin oxidase 2 gene in bread wheat,” Hereditas, vol. 155, no. 33, 2018.
- X. Y. Zhao, P. Hong, J. Y. Wu et al., “The tae-miR408-mediated control of TaTOC1 genes transcription is required for the regulation of heading time in wheat,” Plant Physiology, vol. 170, pp. 1578–1594, 2016.
- F. Barro, J. C. Iehisa, M. J. Giménez et al., “Targeting of prolamins by RNAi in bread wheat: effectiveness of seven silencing-fragment combinations for obtaining lines devoid of coeliac disease epitopes from highly immunogenic gliadins,” Plant Biotechnology Journal, vol. 14, no. 3, pp. 986–996, 2016.
- J. R. Li, W. Zhao, Q. Z. Li et al., “RNA silencing of waxy gene results in low levels of amylose in the seeds of transgenic wheat (triticum aestivum L.),” Acta Genetica Sinica, vol. 32, no. 8, pp. 846–854, 2005.
- S. Yue, H. Li, Y. Li et al., “Generation of transgenic wheat lines with altered expression levels of 1Dx5 high-molecular weight glutenin subunit by RNA interference,” Journal of Cereal Science, vol. 47, no. 2, pp. 153–161, 2008.
- S. B. Altenbach and P. V. Allen, “Transformation of the US bread wheat 'Butte 86' and silencing of omega-5 gliadin genes,” GM Crops, vol. 2, pp. 66–73, 2011.
- S. B. Altenbach, C. K. Tanaka, and B. W. Seabourn, “Silencing of omega-5 gliadins in transgenic wheat eliminates a major source of environmental variability and improves dough mixing properties of flour,” BMC Plant Biology, vol. 14, no. 393, 2014.
- J. Gil-Humanes, F. Pistón, M. J. Giménez et al., “The introgression of RNAi silencing of γ-gliadins into commercial lines of bread wheat changes the mixing and technological properties of the dough,” PLoS ONE, vol. 7, no. 9, article e45937, 2012.
- W. Lee, K. E. Hammond-Kosack, and K. Kanyuka, “Barley stripe mosaic virus-mediated tools for investigating gene function in cereal plants and their pathogens: virus-induced gene silencing, host-mediated gene silencing, and virus-mediated overexpression of heterologous protein,” Plant Physiology, vol. 160, no. 2, pp. 582–590, 2012.
- D. Nowara, A. Gay, C. Lacomme et al., “HIGS: host-induced gene silencing in the obligate biotrophic fungal pathogen Blumeria graminis,” The Plant Cell, vol. 22, no. 9, pp. 3130–3141, 2012.
- W. Cheng, X. Song, H. Li et al., “Host-induced gene silencing of an essential chitin synthase gene confers durable resistance to fusarium head blight and seedling blight in wheat,” Plant Biotechnology Journal, vol. 13, no. 9, pp. 1335–1345, 2015.
- Y. Chen, Q. Gao, M. Huang et al., “Characterization of RNA silencing components in the plant pathogenic fungus fusarium graminearum,” Scientific Reports, vol. 5, no. 12500, 2015.
- X. Song, K. Gu, X. Duan et al., “A myosin5 dsRNA that reduces the fungicide resistance and pathogenicity of fusarium asiaticum,” Pesticide Biochemistry and Physiology, vol. 150, pp. 1–9, 2018.
- X. Zhu, T. Qi, Q. Yang et al., “Host-induced gene silencing of the MAPKK gene PsFUZ7 confers stable resistance to wheat stripe rust,” Plant Physiology, vol. 175, no. 4, pp. 1853–1863, 2017.
- T. Qi, X. Zhu, C. Tan et al., “Host-induced gene silencing of an important pathogenicity factor PsCPK1 in Puccinia striiformis f. sp. tritici enhances resistance of wheat to stripe rust,” Plant Biotechnology Journal, vol. 16, no. 3, pp. 797–807, 2018.
- V. Panwar, M. Jordan, B. McCallum, and G. Bakkeren, “Host-induced silencing of essential genes in Puccinia triticina through transgenic expression of RNAi sequences reduces severity of leaf rust infection in wheat,” Plant Biotechnology Journal, vol. 16, no. 5, pp. 1013–1023, 2018.
- Y. Zhao, X. Sui, L. Xu et al., “Plant-mediated RNAi of grain aphid CHS1 gene confers common wheat resistance against aphids,” Pest Management Science, vol. 74, no. 12, pp. 2754–2760, 2018.
- L. Xu, Q. Hou, Y. Zhao et al., “Silencing of a lipase maturation factor 2-like gene by wheat-mediated RNAi reduces the survivability and reproductive capacity of the grain aphid, sitobion avenae,” Archives of Insect Biochemistry and Physiology, vol. 95, no. 3, article e21392, 2017.
- L. Xu, X. Duan, Y. Lv et al., “Silencing of an aphid carboxylesterase gene by use of plant-mediated RNAi impairs Sitobion avenae tolerance of Phoxim insecticides,” Transgenic Research, vol. 23, no. 2, pp. 389–396, 2014.
- M. Fu, M. Xu, T. Zhou et al., “Transgenic expression of a functional fragment of harpin protein Hpa1 in wheat induces the phloem-based defence against English grain aphid,” Journal of Experimental Botany, vol. 65, no. 6, pp. 1439–1453, 2014.
- E. Abdellatef, T. Will, A. Koch, J. Imani, A. Vilcinskas, and K. Kogel, “Silencing the expression of the salivary sheath protein causes transgenerational feeding suppression in the aphid Sitobion avenae,” Plant Biotechnology Journal, vol. 13, no. 6, pp. 849–857, 2015.
- H. Puchta and F. Fauser, “Gene targeting in plants: 25 years later,” The International Journal of Developmental Biology, vol. 57, no. 6-7-8, pp. 629–637, 2013.
- M. Jinek, K. Chylinski, I. Fonfara, M. Hauer, J. A. Doudna, and E. Charpentier, “A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity,” Science, vol. 337, no. 6096, pp. 816–821, 2012.
- P. Mali, K. M. Esvelt, and G. M. Church, “Cas9 as a versatile tool for engineering biology,” Nature Methods, vol. 10, no. 10, pp. 957–963, 2013.
- Y. Demirci, B. Zhang, and T. Unver, “CRISPR/Cas9: an RNA-guided highly precise synthetic tool for plant genome editing,” Journal of Cellular Physiology, vol. 233, no. 3, pp. 1844–1859, 2018.
- Q. Shan, Y. Wang, J. Li et al., “Targeted genome modification of crop plants using a CRISPR-Cas system,” Nature Biotechnology, vol. 31, pp. 686–688, 2013.
- Q. Shan, Y. Wang, J. Li, and C. Gao, “Genome editing in rice and wheat using the CRISPR/Cas system,” Nature Protocols, vol. 9, no. 10, pp. 2395–2410, 2014.
- S. K. Upadhyay, J. Kumar, A. Alok, and R. Tuli, “RNA-guided genome editing for target gene mutations in wheat,” G3: Genes, Genomes, Genetics, vol. 3, no. 12, pp. 2233–2238, 2013.
- T. Čermák, S. J. Curtin, J. Gil-Humanes et al., “A multi-purpose toolkit to enable advanced genome engineering in plants,” The Plant Cell, vol. 29, pp. 1196–1217, 2017.
- Z. Liang, K. Chen, T. Li et al., “Efficient DNA-free genome editing of bread wheat using CRISPR/Cas9 ribonucleoprotein complexes,” Nature Communications, vol. 8, p. 14261, 2017.
- J. Gil-Humanes, Y. Wang, Z. Liang et al., “High-efficiency gene targeting in hexaploid wheat using DNA replicons and CRISPR/Cas9,” The Plant Journal, vol. 89, no. 6, pp. 1251–1262, 2017.
- Y. Zhang, Y. Bai, G. Wu et al., “Simultaneous modification of three homoeologs of TaEDR1 by genome editing enhances powdery mildew resistance in wheat,” The Plant Journal, vol. 91, no. 4, pp. 714–724, 2017.
- P. Bhowmik, E. Ellison, B. Polley et al., “Targeted mutagenesis in wheat microspores using CRISPR/Cas9,” Scientific Reports, vol. 8, no. 6502, 2018.
- Y. Wang, X. Cheng, Q. Shan et al., “Simultaneous editing of three homoeoalleles in hexaploid bread wheat confers heritable resistance to powdery mildew,” Nature Biotechnology, vol. 32, no. 9, pp. 947–951, 2014.
- Y. Zong, Y. Wang, C. Li et al., “Precise base editing in rice, wheat and maize with a Cas9-cytidine deaminase fusion,” Nature Biotechnology, vol. 35, no. 5, pp. 438–440, 2017.
- Y. Zong, Q. Song, C. Li et al., “Efficient C-to-T base editing in plants using a fusion of nCas9 and human APOBEC3A,” Nature Biotechnology, vol. 36, pp. 950–953, 2018.
- W. Wang, Q. Pan, F. He et al., “Transgenerational CRISPR-Cas9 activity facilitates multiplex gene editing in allopolyploid wheat,” The CRISPR Journal, vol. 1, pp. 65–74, 2018.
- H. Hamada, Y. Liu, Y. Nagira, R. Miki, N. Taoka, and R. Imai, “Biolistic-delivery-based transient CRISPR/Cas9 expression enables in planta genome editing in wheat,” Scientific Reports, vol. 8, no. 14422, 2018.
- M. Singh, M. Kumar, M. C. Albertsen, J. K. Young, and A. M. Cigan, “Concurrent modifications in the three homeologs of Ms45 gene with CRISPR-Cas9 lead to rapid generation of male sterile bread wheat (Triticum aestivum L.),” Plant Molecular Biology, vol. 97, no. 4-5, pp. 371–383, 2018.
- R. M. Howells, M. Craze, S. Bowden, and E. J. Wallington, “Efficient generation of stable, heritable gene edits in wheat using CRISPR/Cas9,” BMC Plant Biology, vol. 18, no. 215, 2018.
- J. Murovec, Ž. Pirc, and B. Yang, “New variants of CRISPR RNA-guided genome editing enzymes,” Plant Biotechnology Journal, vol. 15, no. 8, pp. 917–926, 2017.
- O. O. Abudayyeh, J. S. Gootenberg, P. Essletzbichler et al., “RNA targeting with CRISPR–Cas13,” Nature, vol. 550, no. 7675, pp. 280–284, 2017.
- C. M. Lee, T. J. Cradick, and G. Bao, “The Neisseria meningitides CRISPR-Cas9 system enables specific genome editing in mammalian cells,” Molecular Therapy, vol. 24, no. 3, pp. 645–654, 2016.
- F. A. Ran, L. Cong, W. X. Yan et al., “In vivo genome editing using Staphylococcus aureus Cas9,” Nature, vol. 520, no. 7546, pp. 186–191, 2015.
- E. Kim, T. Koo, S. W. Park et al., “In vivo genome editing with a small Cas9 orthologue derived from Campylobacter jejuni,” Nature Communications, vol. 8, article 14500, 2017.
- C. Li, Y. Zong, Y. Wang et al., “Expanded base editing in rice and wheat using a Cas9-adenosine deaminase fusion,” Genome Biology, vol. 19, no. 59, 2018.
- T. Kelliher, D. Starr, L. Richbourg et al., “MATRILINEAL, a sperm-specific phospholipase, triggers maize haploid induction,” Nature, vol. 542, no. 7639, pp. 105–109, 2017.
- I. Fonfara, H. Richter, M. Bratovič, A. Le Rhun, and E. Charpentier, “The CRISPR-associated DNA-cleaving enzyme Cpf1 also processes precursor CRISPR RNA,” Nature, vol. 532, no. 7600, pp. 517–521, 2016.
- R. Xu, R. Qin, H. Li et al., “Generation of targeted mutant rice using a CRISPR-Cpf1 system,” Plant Biotechnology Journal, vol. 15, no. 6, pp. 713–717, 2017.
- X. Tang, L. G. Lowder, T. Zhang et al., “A CRISPR–Cpf1 system for efficient genome editing and transcriptional repression in plants,” Nature Plants, vol. 3, article 17018, 2017.
- V. J. Nalam, S. Alam, J. Keereetaweep et al., “Facilitation of Fusarium graminearum infection by 9-Lipoxygenases in Arabidopsis and wheat,” Molecular Plant-Microbe Interactions, vol. 28, no. 10, pp. 1142–1152, 2015.
- Y. Zhang, Z. Liang, Y. Zong et al., “Efficient and transgene-free genome editing in wheat through transient expression of CRISPR/Cas9 DNA or RNA,” Nature Communications, vol. 7, Article ID 12617, 2016.
- Z. Liang, K. Chen, Y. Yan, Y. Zhang, and C. Gao, “Genotyping genome-edited mutations in plants using CRISPR ribonucleoprotein complexes,” Plant Biotechnology Journal, vol. 16, no. 12, pp. 2053–2062, 2018.
- S. Lu, H. Zhao, D. L. Des Marais et al., “Arabidopsis ECERIFERUM9 involvement in cuticle formation and maintenance of plant water status,” Plant Physiology, vol. 159, no. 3, pp. 930–944, 2012.
- W. Wang, J. Simmonds, Q. Pan et al., “Gene editing and mutagenesis reveal inter-cultivar differences and additivity in the contribution of TaGW2 homoeologues to grain size and weight in wheat,” Theoretical and Applied Genetics, vol. 131, no. 11, pp. 2463–2475, 2018.
- Q. Li, L. Li, Y. Liu et al., “Influence of TaGW2-6A on seed development in wheat by negatively regulating gibberellin synthesis,” Journal of Plant Sciences, vol. 263, pp. 226–235, 2017.
- H. Xu, M. Zhao, Q. Zhang, Z. Xu, and Q. Xu, “The dense and erect panicle 1 (DEP1) gene offering the potential in the breeding of high-yielding rice,” Breeding Science, vol. 66, no. 5, pp. 659–667, 2016.
- S. Sánchez-León, J. Gil-Humanes, C. V. Ozuna et al., “Low-gluten, nontransgenic wheat engineered with CRISPR/Cas9,” Plant Biotechnology Journal, vol. 16, no. 4, pp. 902–910, 2018.
- “Wheat: vital grain of civilization and food security,” CGIAR Research Program Wheat Annual Report, CGIAR, Mexico, D.F., 2013.
Copyright © 2019 Nikolai Borisjuk et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.