Transgenic Sugarcane Resistant to <i>Sorghum mosaic virus</i> Based on Coat Protein Gene Silencing by RNA Interference

Guo, Jinlong; Gao, Shiwu; Lin, Qinliang; Wang, Hengbo; Que, Youxiong; Xu, Liping

doi:https://doi.org/10.1155/2015/861907

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Volume 2015 | Article ID 861907 | https://doi.org/10.1155/2015/861907

Transgenic Sugarcane Resistant to Sorghum mosaic virus Based on Coat Protein Gene Silencing by RNA Interference

Jinlong Guo,^1,2Shiwu Gao,^1,2Qinliang Lin,^1,2Hengbo Wang,^1,2Youxiong Que,^1,2and Liping Xu^1,2

Academic Editor: Calvin Yu-Chian Chen

Received25 Jun 2014

Revised30 Jul 2014

Accepted21 Aug 2014

Published22 Jan 2015

Abstract

As one of the critical diseases of sugarcane, sugarcane mosaic disease can lead to serious decline in stalk yield and sucrose content. It is mainly caused by Potyvirus sugarcane mosaic virus (SCMV) and/or Sorghum mosaic virus (SrMV), with additional differences in viral strains. RNA interference (RNAi) is a novel strategy for producing viral resistant plants. In this study, based on multiple sequence alignment conducted on genomic sequences of different strains and isolates of SrMV, the conserved region of coat protein (CP) genes was selected as the target gene and the interference sequence with size of 423 bp in length was obtained through PCR amplification. The RNAi vector pGII00-HACP with an expression cassette containing both hairpin interference sequence and cp4-epsps herbicide-tolerant gene was transferred to sugarcane cultivar ROC22 via Agrobacterium-mediated transformation. After herbicide screening, PCR molecular identification, and artificial inoculation challenge, anti-SrMV positive transgenic lines were successfully obtained. SrMV resistance rate of the transgenic lines with the interference sequence was 87.5% based on SrMV challenge by artificial inoculation. The genetically modified SrMV-resistant lines of cultivar ROC22 provide resistant germplasm for breeding lines and can also serve as resistant lines having the same genetic background for study of resistance mechanisms.

1. Introduction

Sugarcane (Saccharum spp. L.), a major sucrose accumulator and biomass producer, is one of the most important field crops grown in the tropics and subtropics [1]. It accounts for 92% of all sugar produced in China [2] and 80% of that in the world. Sugarcane mosaic disease is one of the most serious sugarcane diseases. It primarily damages chloroplasts, blocks photosynthesis, and decreases photosynthetic products, thus resulting in a decline in yield and sugar content [2]. Sugarcane mosaic disease is caused by the sugarcane mosaic virus subgroup of Potyvirus sugarcane mosaic virus (SCMV) and/or Sorghum mosaic virus (SrMV) [3]. Potyvirus is a single-stranded RNA virus, with simple genome structure encoding 10 mature proteins, named from N-terminal to C-terminal: the first protein (P1), helper component proteinase (HC-pro), the third protein (P3), the first 6K protein (6K1), cylindrical inclusion protein (CI), the second 6K protein (6K2), viral protein genome-linked (VPg), nuclear inclusion a protein (NIa), nuclear inclusion b protein (NIb), and coat protein (CP) [4].

The virus strain differentiation is complex, with both of the virus members that cause sugarcane mosaic disease having several different virus strains [5]. At least eight stains have been reported [6], including five from SCMV and three from SrMV. The mixed infection of different virus strains also occurs [3, 6, 7], and dominant virus strains are variable [8]. In the 1980s there were at least three strains of SCMV including strains A, D, and E in mainland China [9]. However, the dominant pathogen has become strain H of SrMV in the last ten years [10]. The simplicity of pathogenic virus genome quickens the change of dominant strains. Coupled with the complexity of the genetic background of sugarcane, the difficulty in the crossbreeding of virus-resistant varieties is obvious, especially for breeding sugarcane varieties resistant to multiple virus strains.

Improving plant antiviral resistance by gene silencing has proven to be effective in several plant-virus biosystems. Abel et al. first transferred CP genes of tobacco mosaic virus (TMV) into tobacco and successfully obtained anti-TMV tobacco plants [11]. Subsequently, different genes in Potyvirus genome were introduced into various plants to obtain corresponding resistant plants [12]. Joyce et al. introduced the CP gene of SCMV into sugarcane, and the CP-transformed plants displayed various phenotypes after SCMV challenge [13]. Ingelbrecht et al. introduced the CP gene of SrMV-H strain into sugarcane and obtained a range of different resistance types [14]. Yao et al. transferred the CP gene of SCMV-E strains into S. officinarum Badila and obtained SCMV-resistant transgenic lines but, after field experiments, found that some of them showed symptoms of mosaic disease, which were shown to be infected with SrMV-H and SCMV by RT-PCR [15]. Therefore, resistance performance of transgenic offspring obtained by the introduction of complete CP genes is complex, and resistance loss to the same or different virus strains in transgenic plants suggests that an improved method is necessary.

Gene silencing through RNA interference (RNAi) appears to be present in most eukaryotic organisms. Homologous RNA is degraded with the introduction of double-stranded RNA (dsRNA), which can lead to target gene silencing [16]. The target gene to be silenced can include a single gene or part sequence of a single gene that is targeted for suppression or can include multiple consecutive segments of a target gene, multiple nonconsecutive segments of a target gene, multiple alleles of a target gene, or multiple target genes from one or more species. RNAi-based antiviral breeding appears to be a promising strategy for development of virus resistance transgenic plants. There have been many successful examples of RNAi-mediated virus resistance improvement in crops, such as soybean [17], tobacco [18, 19], potato [20], barley [21], tomato [22], maize [23], and rice [24]. In sugarcane, the application of RNAi technology to suppress lignin biosynthesis was reported [25, 26], but no study on the application of RNAi technology in improving disease resistance has been reported. SrMV, the pathogen of sugarcane mosaic disease, is a single-stranded RNA virus, which replicates using a viral RNA polymerase. Viral genes in the form of dsRNA generate during replication, which is the basis of using RNAi technology for its control.

In this study, we have used RNAi technology, taking highly conserved sequences of SrMV CP gene as a silencing target, and RNAi expression vector with hairpin structures and introduced them into sugarcane via Agrobacterium-mediated transformation. We then performed screening and biological identification to obtain anti-Sorghum mosaic virus transgenic sugarcane plants. This study provides sugarcane transgenic lines with different resistances in the same genetic background for study of resistance mechanisms and for breeding of multiresistance to various SrMV strains.

2. Materials and Methods

2.1. Bacterial Strains and Plasmids

Escherichia coli strain DH5A, Agrobacterium tumefaciens strain EHA105, and intermediate vector pHANNIBAL were provided by the Key Laboratory of Sugarcane Biology and Genetic Breeding, Ministry of Agriculture (Fuzhou, China). The glyphosate tolerance gene cp4-epsps was obtained from roundup ready soybean by PCR and verified by sequencing, and the intermediate vector pGIIHA containing 35S promoter-cp4-epsps-CaMV polyA cassette was constructed subsequently in previous study.

2.2. Reagents and Plant Materials

Reverse transcriptase (AMV), restriction endonucleases, T4 DNA ligase, and PCR kits were purchased from Fermentas (USA); dephosphorylation (BAP) kit was purchased from Takara (Dalian, China); Wizard DNA clean-up kit gel extraction kit was purchased from Promega Corporation (USA); plant genomic DNA extraction kit was purchased from TIANGEN (Beijing, China); components in MS medium were purchased from Sangon (Shanghai, China); Trizol reagents were purchased from Invitrogen (USA); Timentin disodium salt and 2,4-dichlorophenoxyacetic acid (2-4-D) were purchased from Sigma (USA); and herbicide (47% isopropylamine salt of N-glycine) applicable by foliar spraying was purchased from Sannong Co., Ltd. (Fujian, China). ROC22 was the most popular cultivar in China, which was provided by the Key Laboratory of Sugarcane Biology and Genetic Breeding, Ministry of Agriculture (Fuzhou, China).

2.3. Medium

Infection medium M1 is 1/2 MS + 100 μmol/L acetosyringone + 20 g/L sucrose, pH 5.8; cocultivation medium M2 is 1/2 MS + 3.0 mg/L 2.4-D + 100 μmol/L acetosyringone + 20 g/L sucrose + 5 g/L agar powder, pH 5.8; subculture medium M3 is MS + 3.0 mg/L 2.4-D + 300 mg/L Timentin + 8.0 mg/L herbicide + 30 g/L sucrose + 6 g/L agar powder, pH 5.8; differential medium M4 is MS + 2.0 mg/L BA +0.5 mg/L KT + 0.2 mg/L NAA + 300 mg/L Timentin + 6.0 mg/L herbicide + 30 g/L sucrose + 6 g/L agar powder, pH 5.8; rooting medium M5 is 1/2 MS + 0.2 mg/L 6-BA + 3 mg/L NAA + 60 g/L sucrose + 6 g/L agar powder, pH 5.8.

2.4. RNAi Target Sequence Selection

Genome sequences of the SrMV strains (H, I, and M) isolated from sugarcane were collected from GenBank. Using DNAMAN 5.22 software (http://www.lynnon.com/), multiple sequence alignment was performed to determine the most conservative nucleic acid segment as RNAi target sequence. The fast alignment was generated using DNAMAN 5.22 with default parameters (Gap penalty was set at 7, K-tuple at 3, and number of Top at 5). The accession numbers of the chosen sequences in alignment were EU189035, EU189036, EU189037, EU189041, EU189042, EU189038, EU189043, EU189044, EU189045, EU189046, EU189039, EU189040, U07219, AJ310198, NC004035, and SMU57358 and SrMV FZ strain was kept in our lab (a SrMV strain isolated from Fuzhou, China, unsubmitted).

2.5. Interference Fragment Preparation and Hairpin Intermediate Vector Construction

According to multiple sequence alignment results, a pair of specific primers targeting the most conservative segment were designed, with extra Xba I and Xho I endonuclease restriction sites on the 5′ end of the forward primer CPS and Cla I and Kpn I on the 5′ end of the forward primer CPA. The primer sequences are as follows:

CPS:

5′-GATGTTTGGACAATGATG-3′

CPA:

5′-CTGCACATCAGTGGTTCT-3′

Target sequence for RNAi was amplified by PCR using SrMV FZ as template. The 50 μL PCR reaction mix contained 5.0 μL 10 × PCR buffer, 4.0 μL deoxynucleotide triphosphates (dNTPs) (2.5 mM), 2.0 μL each of forward and reverse primers (10 μM), 2.0 μL template (100 ng), and 0.25 μL Ex-Taq enzyme (5 U/μL). The ddH₂O was added as supplement. The PCR amplification program consisted of predenaturation for 5 min at 94°C, denaturation for 30 s at 94°C, annealing for 30 s at 60°C, and extension for 30 s at 72°C for 30 cycles; final extension was for 10 min at 72°C. The PCR product was purified by gel extraction kit to prepare for digestion. The PCR product was separated in 2% agarose gel. The target DNA fragments were excised and purified using an agarose gel purification kit. Using the two sets of restriction enzymes, Cla I/Xba I and Xho I/Kpn I, successively, the target sequence was inserted into the two sides of the intronic region of pHANNIABL vector. A clone with a recombinant plasmid was validated by PCR, double digestion, and sequencing and was termed as pHANNIABL-CP.

2.6. Construction of the RNAi Expression Vector

The pGIIHA intermediate vector was digested with Not I and then purified by gel extraction kit. The purified products were dephosphorylated according to manual of the dephosphorylation (BAP) kit. Not I-digested hairpin interference cassette fragments from pHANNIBAL-CP were inserted into the Not I site of pGIIHA. A clone with a recombinant plasmid was validated by PCR, double digestion, and sequencing and was termed as pGII00-HACP.

2.7. Preparation of the Engineering Bacteria

According to the freeze-thaw method reported by Holsters et al. [27], the RNAi vector pGII00-HACP was transformed into A. tumefaciens EHA105. The positive clone identified by PCR was inoculated into the LB medium containing kanamycin (50 μg·mL⁻¹) and rifampicin (35 μg·mL⁻¹) for shake culture at 150 rpm at 37°C. When OD₆₀₀ reached 1.0 to 1.2, the culture was centrifuged at 5,000 rpm for 5 min at room temperature to discard the supernatant. The pellet was collected and resuspended with M1 medium and then centrifuged at 5,000 rpm for 5 min at room temperature again to discard the supernatant. The pellet thus obtained was resuspended and diluted with M1 medium to OD₆₀₀ = 1.0.

2.8. Agrobacterium-Mediated Transformation and Screening

Leaf explants from sugarcane ROC22 were cultured on MS medium supplemented with 3.0 mg/L 2,4-D for one week and then cocultivated with recombinant A. tumefaciens EHA105 for 30 min. The plant tissue was picked out and sucked dry with filter paper and cultured on M2 medium for 2-3 d; then the plant tissue was transferred to M3 culture medium and screened for 2-3 generations. After that, the plant tissue was transferred to M4 differential medium, followed by a period of culture on M5 rooting medium when the tissue culture seedlings grew to 4~5 cm in length. The seedlings were then transferred to 72-well nutrition plate when their roots reached about 2.5 cm. After the seedlings were transplanted, the plants were sprayed with liquid herbicide solutions at the concentrations of 3.0 and survivors from the herbicide treatments were selected.

2.9. PCR for Positive Identification

Genome DNA extracted from herbicide-resistant and control plants was diluted to a concentration of 50 ng/μL and was used as PCR template. 35S promoter and cp4-epsps gene were selected as the target genes for identification. Genome DNA of the herbicide-resistant plants was isolated and tested by PCR, using pGII00-HACP as a positive control, genome DNA of untransformed plants as a negative control, and ddH₂O as a blank control.

The primer sequences for the 35S promoter were 35SPro F: 5′-TCTAACAGAACTCGCCGTGAA-3′ and 35Spro R: 5′-AAGGGTCTTGCGAAGGATAGT-3′, and the primers sequences for the cp4-epsps gene were cp4-epsps F: 5′-GTCCTTCATGTTCGGCGGTCTC-3′ and cp4-epsps R: 5′-ACGTCGATGACTTGGCTGGTGA-3′. The 50 μL PCR reaction mix contained 5.0 μL 10 × PCR buffer; 4.0 μL deoxynucleotide triphosphates (dNTPs) (2.5 mM); 2.0 μL each of forward and reverse primers (10 μM); 2.0 μL plasmid DNA (100 ng); and 0.25 μL Ex-Taq enzyme (5 U/μL). The sterile ddH₂O was added as supplement. The PCR amplification program consisted of predenaturation for 5 min at 94°C, denaturation for 30 s at 94°C, annealing for 30 s at 57°C, and extension for 30 s at 72°C for 30 cycles, and final extension was for 10 min at 72°C. The PCR products were separated by 2.0% agarose gel electrophoresis, and the results were analyzed by gel imaging and analysis system.

2.10. Identification of SrMV Resistance by Artificial Inoculation

According to Gómez et al. [28], sugarcane leaves with typical mosaic symptoms were collected and diagnosed with SrMV infection. The artificial inoculation method according to Użarowska et al. [29] used the SrMV-positive leaf samples as the virus infection source.

3. Results and Analysis

3.1. RNAi Target Sequence Selection

Thirteen sequences of the SrMV CP gene and four sequences of the SrMV whole genome in NCBI were selected for multiple sequence alignment analysis. Figure 1 showed that CP genes with 87.39% homology were the most conservative fragment in SrMV genome sequence. Therefore, a conserved region of 423 bp, from 573 bp to 995 bp in CP genes, was identified as the interference fragment sequence.

3.2. Interference Fragment Preparation and Hairpin Intermediate Vector Construction

The target interference fragment with the expected length of 423 bp was obtained by PCR and verified by sequencing. Using the two sets of restriction endonuclease—Kpn I/Xho I or Xba I/Cla I, the 423 bp of partial CP gene and its reverse compliment fragment were successively inserted into each intron site contained in pHANNIBAL and enabled the hairpin intermediate vector pHANNIBAL-CP to make a hairpin loop (Figure 2(a)).

3.3. Construction of RNAi Expression Vector

Recombinant RNAi expression vector was identified by Not I restriction analysis, PCR, and sequencing (data not shown), and the positive hairpin RNAi expression vector was termed as pGII00-HACP (Figure 2(b)).

3.4. Agrobacterium-Mediated Transformation and Screening

The constructed RNAi expression vector pGII00-HACP was transformed into A. tumefaciens EHA105 and used to infect sugarcane calli. After coculture, selective subculture and differentiation culture under herbicide stress, and rooting culture (Figure 3), about five hundred regenerated seedlings were obtained.

(a)

(b)

(c)

(d)

3.5. Herbicide Resistance Screening and PCR Detection of Resistant Regenerated Plants

A portion of the regenerated putative recombinants survived herbicide treatment (Figure 4). Among these, 16 plants from 50 survivors were further identified as positive by PCR, exhibiting existence of 463 bp specific band in the 35S promoter detection and 623 bp specific band in the cp4-epsps gene detection. In order to get more putative resistant transgenic plants, 0.3% herbicide, which was not a complete lethal concentration for sugarcane, was used in this study, although it led to higher false-positive rate. Figure 5 showed part of PCR products identified by gel electrophoresis.

(a)

(b)

3.6. Disease Incidence of Artificially Inoculated Transgenic Lines

After artificial inoculation with SrMV, 14 transgenic plants showed no symptoms and no virus in RT-PCR detection and were judged to be uninfected after SrMV challenge; two transgenic plants and nontransgenic control plants showed symptoms and SrMV in RT-PCR detection, diagnosed as infected after SrMV challenge (Figures 6 and 7). Therefore, it could be concluded that hairpin RNAi expression vector pGII00-HACP, which resulted in production of resistance against SrMV, was successfully introduced into sugarcane and according to 87.5% transgenic plants showed improved resistance to SrMV.

(a)

(b)

(c)

4. Discussion

Mosaic virus-resistant transgenic sugarcane plants have been obtained via particle gun bombardment [14, 15, 30–32], and some transgenic plants were significantly improved in mosaic virus resistance. However, most events produced by gene gun bombardment tend to show high copy numbers of recombinant inserts [33]. Modern sugarcane varieties are a complex allopolyploid and aneuploid genetic background of S. officinarum (chromosome number 80) and S. spontaneum (chromosome number from 40 to 128), with even Erianthus arundinaceus included in sugarcane clones bred during last five years in China [34]. Hence, it was hard to prove clearly characters such as copy numbers, insertion sites, and border sequences in genetically modified (GM) sugarcane via gun bombardment. However, such information is necessary for any GM organisms including GM sugarcane before the application of transgenic field trials. Also high copy numbers of exogenous genes, such as the selective marker, in GM organism can even cause cosuppression [35].

It has been reported that Agrobacterium-mediated transformation leads to clean, discrete, low copy, well-defined, unrearranged DNA insertions into the plant genome [36, 37]. However, Agrobacterium-mediated transformation is not as successful as gene gun bombardment in sugarcane. In the present study, hairpin RNAi expression vector pGII00-HACP was transferred to sugarcane cultivar ROC22 via Agrobacterium-mediated method. The 423 bp interference fragment derived from the most conservative region of the CP gene of SrMV based on multiple alignment analysis of all the three SrMV strains (H, I, and M). The purpose is to obtain multistrains resistant sugarcane plants. In addition, cp4-epsps gene contained in pGII00-HACP can be used as a high-efficiency selective marker and also endows sugarcane with a herbicide-tolerant trait. This enables farmers to make the process of weed control more efficient and flexible.

RNAi is a highly conserved dsRNA-guided mechanism that mediates sequence-specific posttranscriptional gene silencing [38]. As a source of dsRNA, plasmid-expressed short hairpin RNA (shRNA) has been demonstrated to be able to trigger RNAi silencing [21–24]. The study of Varsha Wesley et al. [39] showed that intron-containing constructs (ihpRNA) can generally enable 90–100% of independent transgenic plants to show silencing. The average percentages of ihpRNA, hpRNA, cosuppression, and antisense constructs at silencing were 90%, 58%, 13%, and 12%, respectively [39]. pHANNIBAL, an intermediate generic vector used in this study, allows a simple, single PCR product from CP gene to be easily converted into a highly effective ihpRNA silencing construct. Similar to Varsha Wesley et al. [39], the ihpRNA silencing construct targeting SrMV CP gene in this study exhibited 87.5% high silencing effect.

In summary, a 423 bp highly conserved region from the CP gene of SrMV was selected as the interference sequence based on multiple alignment analysis of all the three SrMV strains (H, I, and M) and several other isolates. The hairpin RNAi expression vector pGII00-HACP was transferred to sugarcane cultivar ROC22 via Agrobacterium-mediated transformation. After herbicide screening, PCR molecular identification, and artificial inoculation challenge, anti-SrMV positive transgenic lines were successfully obtained. This study provides the foundation for a further study on silencing mechanism of SrMV-CP gene expression based on RNA interference and provides novel materials to evaluate the silencing effect connected with exogenous gene copy numbers and insertion sites. It also provides new material for broad-spectrum antiviral sugarcane breeding.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Authors’ Contribution

Jinlong Guo and Shiwu Gao equally contributed to this paper.

Acknowledgments

This work was supported by the National Natural Science Foundation of China (30871581), the Earmarked Fund for the Modern Agroindustry Technology Research System (CARS-20), and the 948 Program on the Introduction of International Advanced Agricultural Science and Techniques of the Department of Agriculture (2014-S18).

References

J. L. Guo, L. P. Xu, Y. C. Su et al., “ScMT2-1-3, a metallothionein gene of sugarcane, plays an important role in the regulation of heavy metal tolerance/accumulation,” BioMed Research International, vol. 2013, Article ID 904769, 12 pages, 2013.
View at: Publisher Site | Google Scholar
R. K. Chen, L. P. Xu, Y. Q. Lin et al., Chinese Monograph: Modern Sugarcane Genetic Breeding, China Agriculture Press, 2011.
Y. Xie, M. Wang, D. Xu, R. Li, and G. Zhou, “Simultaneous detection and identification of four sugarcane viruses by one-step RT-PCR,” Journal of Virological Methods, vol. 162, no. 1-2, pp. 64–68, 2009.
View at: Publisher Site | Google Scholar
F. Revers, O. L. Gall, T. Candresse, and A. J. Maule, “New advances in understanding the molecular biology of plant/potyvirus interactions,” Molecular Plant-Microbe Interactions, vol. 12, no. 5, pp. 367–376, 1999.
View at: Publisher Site | Google Scholar
Z. N. Yang and T. E. Mirkov, “Sequence and relationships of sugarcane mosaic and sorghum mosaic virus strains and development of RT-PCR-based RFLPS for strain discrimination,” Phytopathology, vol. 87, no. 9, pp. 932–939, 1997.
View at: Publisher Site | Google Scholar
V. R. Mali and R. P. Thakur, “Natural infection of sugarcane by an immunity breaking strain of sorghum mosaic potyvirus (SR MV-IBS) in peninsular India,” Sugar Tech, vol. 2, no. 3, pp. 20–25, 2000.
View at: Google Scholar
C. G. Marcos, P. R. Luciana, C. S. Silvana, and G. A. L. Marcros, “Virus diseases of sugarcane A constant challenge to sugarcane breeding in Brazil,” Functional Plant Science and Biotechnology, vol. 6, pp. 108–112, 2012.
View at: Google Scholar
M. P. Grisham and Y.-B. Pan, “A genetic shift in the virus strains that cause mosaic in Louisiana sugarcane,” Plant Disease, vol. 91, no. 4, pp. 453–458, 2007.
View at: Publisher Site | Google Scholar
Y. H. Chen, Z. J. Zhou, Q. Y. Lin, and L. H. Xie, “A preliminary report on strains of sugarcane mosaic virus,” Chinese Journal: Journal of Fujian Agriculture College, vol. 17, no. 1, pp. 44–48, 1988.
View at: Google Scholar
Y. Guo, “Identification of the viral pathogen of sugarcane mosaic disease in 4 sugarcane planting states of China and gene analysis of virus protein,” in Chinese Degree: Fujian Agriculture and Forestry University, Supervisor: M. Q. Zhang, pp. 26–27, 2008.
View at: Google Scholar
P. P. Abel, R. S. Nelson, B. de et al., “Delay of disease development in transgenic plants that express the tobacco mosaic virus coat protein gene,” Science, vol. 232, no. 4751, pp. 738–743, 1986.
View at: Publisher Site | Google Scholar
E. Gammelgård, M. Mohan, and J. P. T. Valkonen, “Potyvirus-induced gene silencing: the dynamic process of systemic silencing and silencing suppression,” Journal of General Virology, vol. 88, no. 8, pp. 2337–2346, 2007.
View at: Publisher Site | Google Scholar
P. A. Joyce, R. B. McQualter, J. A. Handley, J. L. Dale, R. M. Harding, and G. R. Smith, “Transgenic sugarcane resistant to sugarcane mosaic virus,” in Proceedings of the 20th Conference of the Australian Society of Sugar Cane Technologists, Ballina, Australia, 1998.
View at: Google Scholar
I. L. Ingelbrecht, J. E. Irvine, and T. E. Mirkov, “Posttranscriptional gene silencing in transgenic sugarcane. Dissection of homology-dependent virus resistance in a monocot that has a complex polyploid genome,” Plant Physiology, vol. 119, no. 4, pp. 1187–1198, 1999.
View at: Publisher Site | Google Scholar
W. Yao, A. L. Yu, J. S. Xu, G. L. Geng, M. Q. Zhang, and R. K. Chen, “Analysis and identification for transgenic sugarcane of ScMV-CP gene,” Chinese Journal of Molecular Plant Breeding, vol. 2, no. 1, pp. 13–18, 2004.
View at: Google Scholar
A. Aigner, “Gene silencing through RNA interference (RNAi) in vivo: strategies based on the direct application of siRNAs,” Journal of Biotechnology, vol. 124, no. 1, pp. 12–25, 2006.
View at: Publisher Site | Google Scholar
H. J. Kim, M.-J. Kim, J. H. Pak et al., “Characterization of SMV resistance of soybean produced by genetic transformation of SMV-CP gene in RNAi,” Plant Biotechnology Reports, vol. 7, no. 4, pp. 425–433, 2013.
View at: Publisher Site | Google Scholar
Y. B. Niu, D. F. Wang, M. Yao, Z. Yan, and W. X. You, “Transgenic tobacco plants resistant to two viruses via RNA silencing,” Acta Agronomica Sinica, vol. 37, no. 3, pp. 484–488, 2011.
View at: Google Scholar
E. Bucher, D. Lohuis, P. M. J. A. van Poppel, C. Geerts-Dimitriadou, R. Goldbach, and M. Prins, “Multiple virus resistance at a high frequency using a single transgene construct,” Journal of General Virology, vol. 87, no. 12, pp. 3697–3701, 2006.
View at: Publisher Site | Google Scholar
V. O. Ntui, K. Kynet, P. Azadi et al., “Transgenic accumulation of a defective cucumber mosaic virus (CMV) replicase derived double stranded RNA modulates plant defence against CMV strains O and Y in potato,” Transgenic Research, vol. 22, no. 6, pp. 1191–1205, 2013.
View at: Publisher Site | Google Scholar
M.-B. Wang, D. C. Abbott, and P. M. Waterhouse, “A single copy of a virus-derived transgene encoding hairpin RNA gives immunity to barley yellow dwarf virus,” Molecular Plant Pathology, vol. 1, no. 6, pp. 347–356, 2000.
View at: Publisher Site | Google Scholar
C.-Y. Lin, H.-M. Ku, W.-S. Tsai, S. K. Green, and F.-J. Jan, “Resistance to a DNA and a RNA virus in transgenic plants by using a single chimeric transgene construct,” Transgenic Research, vol. 20, no. 2, pp. 261–270, 2011.
View at: Publisher Site | Google Scholar
Z.-Y. Zhang, L. Yang, S.-F. Zhou, H.-G. Wang, W.-C. Li, and F.-L. Fu, “Improvement of resistance to maize dwarf mosaic virus mediated by transgenic RNA interference,” Journal of Biotechnology, vol. 153, no. 3-4, pp. 181–187, 2011.
View at: Publisher Site | Google Scholar
T. Shimizu, E. Nakazono-Nagaoka, F. Akita et al., “Hairpin RNA derived from the gene for Pns9, a viroplasm matrix protein of Rice gall dwarf virus, confers strong resistance to virus infection in transgenic rice plants,” Journal of Biotechnology, vol. 157, no. 3, pp. 421–427, 2012.
View at: Publisher Site | Google Scholar
K. Osabe, S. R. Mudge, M. W. Graham, and R. G. Birch, “RNAi mediated down-regulation of PDS gene expression in sugarcane (Saccharum), a highly polyploid crop,” Tropical Plant Biology, vol. 2, no. 3, pp. 143–148, 2009.
View at: Publisher Site | Google Scholar
J. H. Jung, W. M. Fouad, W. Vermerris, M. Gallo, and F. Altpeter, “RNAi suppression of lignin biosynthesis in sugarcane reduces recalcitrance for biofuel production from lignocellulosic biomass,” Plant Biotechnology Journal, vol. 10, no. 9, pp. 1067–1076, 2012.
View at: Publisher Site | Google Scholar
M. Holsters, D. de Waele, A. Depicker, E. Messens, M. van Montagu, and J. Schell, “Transfection and transformation of Agrobacterium tumefaciens,” Molecular & General Genetics, vol. 163, no. 2, pp. 181–187, 1978.
View at: Publisher Site | Google Scholar
M. Gómez, A. M. Rago, and G. Serino, “Rapid identification of viruses causing sugarcane mosaic by direct sequencing of RT-PCR products from crude extracts: a method for large scale virus surveys,” Journal of Virological Methods, vol. 157, no. 2, pp. 188–194, 2009.
View at: Publisher Site | Google Scholar
A. Użarowska, G. Dionisio, B. Sarholz et al., “Validation of candidate genes putatively associated with resistance to SCMV and MDMV in maize (Zea mays L.) by expression profiling,” BMC Plant Biology, vol. 9, article 15, 2009.
View at: Publisher Site | Google Scholar
G. R. Smith, R. L. Gambley, and B. T. Egan, “Progress in development of a sugarcane meristem transformation system and production of SCMV-resistant transgenics,” Proceedings of the Australian Society of Sugar Cane Technologists, vol. 15, pp. 237–250, 1994.
View at: Google Scholar
R. A. Gilbert, M. Gallo-Meagher, J. C. Comstock, J. D. Miller, M. Jain, and A. Abouzid, “Agronomic evaluation of sugarcane lines transformed for resistance to Sugarcane mosaic virus strain E,” Crop Science, vol. 45, no. 5, pp. 2060–2067, 2005.
View at: Publisher Site | Google Scholar
Y. Guo, M. H. Ruan, W. Yao, L. Chen, R. K. Chen, and M. Q. Zhang, “Difference of coat protein mediated resistance to sugarcane mosaic virus between Badila and Funong 91–4621,” Journal of Fujian Agriculture and Forestry University (Natural Science Edition), vol. 37, no. 1, pp. 7–12, 2008 (Chinese).
View at: Google Scholar
A. D. Arencibia, E. R. Carmona, P. Téllez et al., “An efficient protocol for sugarcane (Saccharum spp. L.) transformation mediated by Agrobacterium tumefaciens,” Transgenic Research, vol. 7, no. 3, pp. 213–222, 1998.
View at: Publisher Site | Google Scholar
B. Xue, J. Guo, Y. Que, Z. Fu, L. Wu, and L. Xu, “Selection of suitable endogenous reference genes for relative copy number detection in sugarcane,” International Journal of Molecular Sciences, vol. 15, no. 5, pp. 8846–8862, 2014.
View at: Publisher Site | Google Scholar
W. Tang, R. J. Newton, and D. A. Weidner, “Genetic transformation and gene silencing mediated by multiple copies of a transgene in eastern white pine,” Journal of Experimental Botany, vol. 58, no. 3, pp. 545–554, 2007.
View at: Publisher Site | Google Scholar
A. R. Wenck, M. Quinn, R. W. Whetten, G. Pullman, and R. Sederoff, “High-efficiency agrobacterium-mediated transformation of Norway spruce (Picea abies) and loblolly pine (Pinus taeda),” Plant Molecular Biology, vol. 39, no. 3, pp. 407–416, 1999.
View at: Publisher Site | Google Scholar
M. N. Somleva, Z. Tomaszewski, and B. V. Conger, “Agrobacterium-mediated genetic transformation of switchgrass,” Crop Science, vol. 42, no. 6, pp. 2080–2087, 2002.
View at: Publisher Site | Google Scholar
G. Meister and T. Tuschl, “Mechanisms of gene silencing by double-stranded RNA,” Nature, vol. 431, no. 7006, pp. 343–349, 2004.
View at: Publisher Site | Google Scholar
S. Varsha Wesley, C. A. Helliwell, N. A. Smith et al., “Construct design for efficient, effective and high-throughput gene silencing in plants,” Plant Journal, vol. 27, no. 6, pp. 581–590, 2001.
View at: Publisher Site | Google Scholar

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Copyright © 2015 Jinlong Guo 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.

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