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International Journal of Evolutionary Biology
Volume 2012 (2012), Article ID 490894, 8 pages
The Evolution of Novelty in Conserved Gene Families
Department for Evolutionary Biology, Max Planck Institute for Developmental Biology, Spemannstraße 37, 72076 Tübingen, Germany
Received 16 March 2012; Accepted 23 April 2012
Academic Editor: Frédéric Brunet
Copyright © 2012 Gabriel V. Markov and Ralf J. Sommer. 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.
One of the major aims of contemporary evolutionary biology is the understanding of the current pattern of biological diversity. This involves, first, the description of character distribution at various nodes of the phylogenetic tree of life and, second, the functional explanation of such changes. The analysis of character distribution is a powerful tool at both the morphological and molecular levels. Recent high-throughput sequencing approaches provide new opportunities to study the genetic architecture of organisms at the genome-wide level. In eukaryotes, one overarching finding is the absence of simple correlations of gene count and biological complexity. Instead, the domain architecture of proteins is becoming a central focus for large-scale evolutionary innovations. Here, we review examples of the evolution of novelty in conserved gene families in insects and nematodes. We highlight how in the absence of whole-genome duplications molecular novelty can arise, how members of gene families have diversified at distinct mechanistic levels, and how gene expression can be maintained in the context of multiple innovations in regulatory mechanisms.
To understand evolutionary novelty and its contribution to the generation of new species, biologists search for character differences between closely related species and try to determine the functional meaning of such changes. Characters range from morphological traits, like the trichome pattern on the cuticle of a fruit fly larva, to molecular characters such as nucleotide sequences. The genomics era is now providing an increasing number and also new kinds of molecular characters, such as gene numbers in multigenic families, gene position on chromosomes, microRNAs, or insertions of mobile elements at various places in a genome. In addition, next-generation sequencing approaches provide genome-wide single-nucleotide polymorphism (SNP) and copy number variation (CNV) data in a number of model organisms . Nonetheless, it remains challenging to articulate knowledge concerning all these characters in a comprehensive functional framework. While there are some cases with a direct link between various levels of character changes, such as the small number of single-nucleotide mutations in a transcriptional enhancer that can modify the trichome pattern on the larval cuticle in Drosophila sechellia , there are many other cases where great variation at the molecular level has no simply interpretable effect at the level of the organism. Although this does not mean that such changes are necessarily neutral, there is a strong tendency to correlate any unexpected genomic finding, such as genome duplication or peculiar gene family expansion, with an adaptation to special environmental conditions, often without proper justification . These attempts reflect an understandable quest for generalization. It was recently stressed that evolutionary relevant mutations are not distributed at random in the genome, and that a precise understanding of the contribution of genetic factors to evolution requires the consideration of the specific functional properties of genes . One aspect that is often forgotten in these discussions is that cross-genome comparisons between species are mostly challenged by the inherent difficulty to infer homology between deeply rooted species [3–5].
Here, we review some cases where spectacular molecular changes do not correlate with any clear phenotypic novelty at the organismal level, and we highlight the need to cope with different types of variation to understand their reciprocal interactions. We will review three examples dealing with (i) novelty by genome diversification in the absence of whole-genome duplication, (ii) novelty in large gene families, and (iii) novelty in promoter regions. For practical reasons, we focus our example choices on ecdysozoans, an animal group that contains two of the best genetic models, the fruit fly Drosophila melanogaster and the nematode worm Caenorhabditis elegans, each of which is complemented by satellite organisms, allowing us to make sophisticated comparisons by functional investigations .
2. Genome Diversification in the Absence of Whole-Genome Duplication
The spectacular examples of land plants and vertebrates highlight the importance of genome duplications for evolutionary success measured in a number of ways, such as number of species, morphological innovations, and ecological diversification . In the animals, however, two other phyla outcompete the vertebrates in all these characteristics. Insects and nematodes are the largest animal phyla with respect to species number as well as morphological and ecological diversification [8, 9]. It is often forgotten that they managed to reach the highest levels of species diversity among animals without the involvement of genome duplication. At the same time, it has to be stressed that the absence of genome duplications in insects and nematodes does not mean that these two groups are lacking noticeable genomic innovations. For example, genome-wide comparisons of aminoacid substitution patterns lead to the estimate that the 39-million-year time interval between the separation of dipterans and coleopterans and the split of the two main dipteran lineages was characterized by an episodic threefold increase in evolutionary rate relative to the mean rate found for the coleopteran representative Tribolium castaneum . It was then established that lepidopterans have branches of similar length than dipterans, whereas other holometabolous insects have shorter branches, indicating substitution rates comparable to those of coleopterans [11, 12]. Both dipterans and lepidopterans are, along with a three less diverse orders, members of an insect clade called “Mecopterida” (Table 1), and members of these three orders also experienced a strong acceleration of aminoacid substitution rate at least for the ecdysone receptor gene, a major regulator of molting . Taken together, these data suggest that the acceleration of evolutionary rate took place at the stem of Mecopterida. Interestingly, the interaction between the two proteins that make the ecdysone receptor, USP and EcR, was conserved in spite of the acceleration, because it was compensated by the acquisition of a new dimerization surface that stabilized both partners . The fact that the name “Mecopterida” is almost unknown outside entomology circles illustrates the absence of correlation between this strong molecular divergence and any major phenotypic change. In contrast, the two other species-rich insect orders, hymenopterans and coleopterans, have not experienced such a genome-wide acceleration, indicating that the understanding of this process will require more than a simplistic adaptationist scenario.
In nematodes, similar findings can be made. For example, in the major nematode model species C. elegans, one of the most salient genomic features is the presence of some protein families with high numbers of duplications or coding genes. This is the case for the hedgehog-related sterol-binding secreted signaling proteins , which are mainly expressed in cuticular cells . It is also the case for the guanylyl cyclases , tyrosine kinases , seven-transmembrane receptors , and nuclear receptors , as well as a number of other families that have not been studied specifically in nematodes. The analysis of members of multigene families that duplicated early in metazoan evolution or even before requires detailed phylogenetic investigations of each of these families, which is not always available. Therefore, it is still impossible to provide a comprehensive overview of genome diversification based on single-gene duplications. Moreover, the precise functional meaning of such amplifications remains quite obscure, even if these expansions show readily discernible patterns.
The functional gene categories most prone to lineage-specific expansions in eukaryotes seem to be structural proteins. This involves enzymes functioning in response to pathogens and environmental stress and includes various components of signaling pathways responsible for specificity, such as ubiquitin ligase subunits and transcription factors . While the duplication pattern of nematode genes is roughly consistent with this notion, lineage-specific variations also exist, especially concerning the spatial distribution of duplicates in the genome. In C. elegans, for example, the number of duplicates varies greatly depending on the chromosomal location. The highest concentration of duplicates is found on chromosome V, which reflects tandem amplification in a specifically dynamic chromosomal context and indicates that purely structural factors can also drive the pattern of gene duplication pattern . At least in C. elegans and its close relative C. briggsae, there is a strong difference with regard to the position along the chromosome, as duplicated genes are more abundant in the chromosomal arms than in the centromeric part [23–25].
Apart from gene duplications, a major unexpected outcome of nematode genome sequencing is the importance of horizontal gene transfer (HGT), a process that was previously thought to be rare among eukaryotes with sexual reproduction. It turns out that many genes encoding for plant cell-wall modifying proteins were acquired in some nematode lineages many times independently and from various donor organisms [26–28]. Recipients of HGT-acquired cell-wall modifying proteins were plant-parasitic nematodes of the genera Bursaphelenchus, Meloidogyne, Heterodera, Globodera, Pratylenchus, and Xiphinema (for review, see ). Additionally, some nonplant parasitic nematodes such as the necromenic species Pristionchus pacificus have obtained cellulases from protist-type donors .
A major bottleneck for better understanding gene duplications and other processes such as HGT in their short-term and long-term evolutionary consequences is the lack of precise functional knowledge about the majority of these paralogous genes. This includes the well-studied genetic model system C. elegans. Compounded with the absence of functional genetic data for many paralogous genes is that little is known about the population structure and polymorphism rates in C. elegans. For example, when positive selection was detected among the srz family (the Z family of the serpentine receptor superfamily), where no protein had a precisely known physiological function, there were no additional data that would help to interpret the meaning of this observation . This represents an important challenge for future studies because pure computational detection of candidate gene for positive selection is not sufficient to ascertain that an evolutionary event has a real functional meaning. Indeed, the frequency of adaptative substitutions can sometimes be overestimated due to the interplay of other processes that also influence the frequency of nucleotide substitutions, such as genetic hitchhiking or epistatic effects between nonindependent sites, processes of which vary greatly among lineages .
Biases in codon composition that are taken as molecular signatures for positive selection can also be produced by a specific bias in DNA turnover at that particular part of the genome. Such a mechanism was already suggested 30 years ago under the concept “molecular drive”  and got further support by whole-genome studies on the distribution of sites that are predicted to be under positive selection [34, 35]. Advances in population-genetic theory showed the emergence of certain kinds of aminoacid substitutions and protein-protein complexes restricted to taxa with relatively small effective population sizes . Besides this structure-driven effect of gene family amplification, one should also take into account the possibility that the structure of some signaling networks necessitates the retention of duplicates, similar to what occurs in Mecopterida, where many members of the same ecdysone-signaling network have undergone a supplemental acceleration in nucleotide turnover when compared to the rest of the genome . Furthermore, it should be noted that following an original gene duplication, “new” functions that arise subsequently are not really new but represent cases of subfunctionalization and cooption . In addition, it has recently been proposed that there is no definitive proof that orthologous genes are functionally more similar than closely related paralogs . Comparisons of aminoacid substitution patterns between the speciation event that separated insects and chordates and the duplication event at the basis of vertebrate show similar trends, suggesting that speciation is as important as duplication to promote novelty in gene families .
Taken together, genome-wide analyses of species-rich groups of insects and nematodes have identified mechanisms by which genomes can diversify to create novelty in the absence of complete genome duplications. Although both groups show an extraordinary level of genome data and have been studied by the scientific community for more than a century, the functional understanding of genes is often limited. Given space restrictions, we are unable to discuss fully the many hypotheses that have been proposed in association with the limitations of our current understanding, and so we refer the reader to cited literature for more in depth discussions.
3. A Case Study: Molecular Novelty in a Conserved Gene Family
Gene families have been identified as a major target for the generation of molecular novelty in eukaryotes. One of the gene families with a spectacular duplication rate is the nuclear receptor family. In nematodes, for example, the majority of duplicates arose from the amplification of a single member of the family, named HNF4 (NR2A), up to more than 250 duplicates in C. elegans . In general, nuclear receptors are currently defined as ligand-activated transcription factors that can undergo a conformational change in response to the binding of a small molecule . Some studies based on ancestral sequence reconstruction and in vitro analysis document up to the level of individual mutations how innovations in ligand-binding ability have arisen [43, 44]. This family is one of the most stable at the metazoan level, its members showing a conserved modular structure comprising a DNA-binding domain and a ligand-binding domain that are well characterized at the structural level . However, even among nuclear receptors, there are some atypical members that can have important functional roles in spite of an altered functional structure (Figure 1). For example, the vertebrate DAX-1 (NR0B) is a receptor that has no DNA-binding domain. It is involved in X-linked adrenal hypoplasia congenita, a developmental disorder of the human adrenal gland, where it acts as a dominant-negative receptor that blocks the activation ability of other nuclear receptors . In Drosophila, a similar situation appears during the molting cycle. One of the receptors involved in the regulation of molting, E75 (NR1D), has many isoforms that are expressed at various stages in the molting cycle. The isoform E75B lacks half of its DNA-binding domain, having only one zinc finger instead of two for a canonical DNA-binding domain. Being itself unable to bind DNA, it acts as a transcriptional repressor by blocking the transactivation abilities of its dimerization partner . This example nicely demonstrates that even a single gene can give rise to proteins with different and even antagonistic functions, due to the variability generated by alternative splicing.
Other members of the nuclear receptor family are devoid of a ligand-binding domain. This is the case for the developmental control gene knirps (NR0A1), a Drosophila segmentation gene whose expression in the posterior part of the fly embryo is responsible for the presence of abdominal segments 1–7 . It is also involved in head morphogenesis and in tracheal formation later in development. Interestingly, some of its functions in late development are redundant with those of its close paralog knrl , but the greater intron size of knrl relative to knirps prevents it from functional complementation duringsegmentation, where transcription time during short mitotic cycles provides a physiological barrier to transcript size . While both genes arose from a duplication event in the cyclorrhaphan diptera, their nonduplicated ortholog in Tribolium castaneum also plays a role that is essential for head patterning .
Such a patterning role of nuclear receptors during insect segmentation is not restricted to receptors that have lost their ligand-binding domain but can also be observed in the orphan receptor encoded by the tailless gene (NR2E2). This protein has a recognizable ligand-binding domain but no known ligand. In Drosophila, this transcription factor belongs to the segmentation genes like knirps, and it functions in the segmentation gene hierarchy by providing an early subdivision into groups of segments of the embryo by acting as a transcriptional repressor . This function seems to be conserved among holometabolous insects . However, the most conserved part of tailless function seems to be its role in the specification of the anterior nervous system (Figure 2). In Drosophila, tailless controls the formation of the protocerebral neuroblasts and acts in eye formation . In mammals, it is involved in brain and visual system development, as well as in neural stem-cell renewal at the adult stage . In C. elegans, the tailless ortholog, named nhr-67, is expressed in six head neurons, but is also involved in other processes, such as the patterning of the vulva  and the control of the migration of the linker cell in the male gonad .
All these examples from nuclear receptors that do not act as ligand-activated transcription factors show that even in a family that is very well conserved at the structural level, there can be many functional variations and novelty. These unusual cases are involved in the control of important biological processes, providing a powerful first glance at the complexity of eukaryotic genomes. One should be aware, however, that such studies can lead only to partial conclusions, which need to be completed by more precise functional investigations. The genes described above, like any other gene in eukaryotic genomes, might have acquired novel but simple protein domains, that are not easily detectable by bioinformatic means. For example, the origin of four amino acid SH3-binding domains in an otherwise conserved LIN-18/Ryk/derailed receptor in WNT signaling has allowed new wiring in the signaling pathway leading to vulva formation in the nematode Pristionchus pacificus but which is not present in C. elegans . Such domains would go unnoticed without functional studies by unbiased genetic approaches.
4. cis -Regulatory Novelties in the Promoter of a Gene with Conserved Expression Pattern
In the recent years, there has been an ongoing debate about the contribution of cis-regulatory elements versus protein-coding regions in evolutionary innovation [59, 60]. The arguments are extensively reviewed in detail elsewhere , so we will concentrate on the complementary side of the problem, the fact that high promoter turnover and changes in transcriptional regulation are compatible with a conserved gene expression pattern.
The evolution of the promoter of the tailless gene is especially well studied in holometabolous insects (Figure 2). The expression of the tailless gene in Drosophila melanogaster is regulated by a complex set of transcription factors, the most important being bicoid  and two other genes that are in the downstream torso signaling pathway . The promoter of another dipteran fly, Musca domestica, contains binding sites for all these transcription factors in similar numbers, although the binding sites are organized in a different order. The expression of tailless is highly similar in the two flies at the blastodermal stage , the only subtle difference being the split of the expression pattern in the anterior cap from the Musca embryo, which does not occur in Drosophila. Additionally, the promoter of Musca is able to drive a Drosophila-like expression pattern of a reporter gene when inserted in Drosophila embryos . These observations completed by estimations about the mutation rates in Drosophila gene promoters suggest that the promoter region was fully renewed during the 100 million years following the divergence of Drosophila and Musca . It has therefore been argued that the regulation by the same transcription factors was maintained by constant loss and de novo acquisitions of similar promoter elements .
In the flour beetle Tribolium castaneum, the expression pattern of tailless during embryogenesis is similar to that in flies, and the activation by the torso pathway is conserved as well. In contrast, transcriptional control by bicoid is not possible, because bicoid is specific to flies . In contrast to flies and beetles, hymenopterans represent again a different case. In the parasitic wasp Nasonia vitripennis, in which components of the torso pathway are missing, the expression of tailless is activated by orthodenticle-1 . In the honeybee Apis mellifera, anterior expression of tailless also depends on orthodenticle-1, but its posterior expression is due to maternal RNA . A contribution of orthodenticle-1 to tailless expression also in T. castaneum is likely, given the fact that orthodenticle-1 is a proposed substitute for bicoid in this insect , but direct binding from orthodenticle-1 to the tailless promoter is yet to be reported. In spite of this remaining question, the comparison of the regulatory mechanisms for the tailless expression shows that there are already four slightly different ways that are known to maintain this pattern in holometabolous insects.
The tailless case is particularly well documented in terms of species sampling. Yet there are many other examples of high promoter turnover in genes whose expression is conserved (reviewed in ). This illustrates the notion of developmental system drift, describing the fact that many changes in developmental pathways occur during evolution without phenotypic effect and thus are more likely to be the result of contingent historical events than the response to selection pressure .
In his autobiography, Darwin  wrote the following about the reasons that pushed him to write two extensive monographies about cirripedes: ‘‘When on the coast of Chile, I found a most curious form, which burrowed into the shells of Concholepas, and which differed so much from all other Cirripedes that I had to form a new sub-order for its sole reception. […] To understand the structure of my new Cirripede, I had to examine and dissect many of the common forms: and this gradually led me on to take up the whole group.’’ This illustrates perfectly well what lies on the agenda of today’s evolutionary biologists. What has changed since Darwin’s time is that now we have the tools required to describe natural variation from the molecular level to the ecological one. It follows that, for a given node of a phylogenetic tree, variation and repartition of characters can and need to be addressed at all these levels. What we have to understand is the connection between the various layers of biological complexity, combining and integrating the results of laboratory and fieldwork approaches .
We argue that the partial data on genomic variation are already sufficient to indicate that no specific attribute of a given molecular structure can indicate a priori more potentials than others to contribute to novelty at a higher phenotypic level. Uncoupling and buffering of natural variation at various integration scales has been clearly demonstrated, implying that the number of molecular events that can be directly correlated with a phenotypic change at the organismal level is probably very low, and that they are the results of exceptional contingency and structural constraints . The possibility to detect de novo such interesting changes in nonmodel organisms is thus also probably very low, and it decreases quickly with an increase of the phylogenetic distance. Additionally, one should not forget that to really understand the link between genetic variation and phenotypic diversity, it is necessary to be able to explain cases where a molecular change triggers novelty, and those where phenotypic traits are maintained in spite of molecular innovations in the genes that specify them.
The authors thank members of the Sommer Lab for discussions and Dr. Erik J. Ragsdale for carefully reading the paper. This work was supported by funding from the Max Planck Society.
- M. Nordborg and D. Weigel, “Next-generation genetics in plants,” Nature, vol. 456, no. 7223, pp. 720–723, 2008.
- N. S. Frankel, D. F. Erezyilmaz, A. P. McGregor, S. Wang, F. Payre, and D. L. Stern, “Morphological evolution caused by many subtle-effect substitutions in regulatory DNA,” Nature, vol. 474, no. 7353, pp. 598–603, 2011.
- M. Lynch, “The frailty of adaptive hypotheses for the origins of organismal complexity,” Proceedings of the National Academy of Sciences of the United States of America, vol. 104, no. 1, pp. 8597–8604, 2007.
- D. L. Stern and V. Orgogozo, “Is genetic evolution predictable?” Science, vol. 323, no. 5915, pp. 746–751, 2009.
- R. J. Sommer, “Homology and the hierarchy of biological systems,” BioEssays, vol. 30, no. 7, pp. 653–658, 2008.
- R. J. Sommer, “The future of evo-devo: model systems and evolutionary theory,” Nature Reviews Genetics, vol. 10, no. 6, pp. 416–422, 2009.
- Y. Van De Peer, S. Maere, and A. Meyer, “The evolutionary significance of ancient genome duplications,” Nature Reviews Genetics, vol. 10, no. 10, pp. 725–732, 2009.
- D. Grimaldi and M. S. Engel, Evolution of the Insects, Cambridge University Press, Cambridge, UK, 2005.
- D. L. Lee, Ed., The Biology of Nematodes, Taylor & Francis, London, UK, 2002.
- J. Savard, D. Tautz, and M. J. Lercher, “Genome-wide acceleration of protein evolution in flies (Diptera),” BMC Evolutionary Biology, vol. 6, article 7, 2006.
- J. Savard, D. Tautz, S. Richards et al., “Phylogenomic analysis reveals bees and wasps (Hymenoptera) at the base of the radiation of Holometabolous insects,” Genome Research, vol. 16, no. 11, pp. 1334–1338, 2006.
- E. M. Zdobnov and P. Bork, “Quantification of insect genome divergence,” Trends in Genetics, vol. 23, no. 1, pp. 16–20, 2007.
- F. Bonneton, F. G. Brunet, J. Kathirithamby, and V. Laudet, “The rapid divergence of the ecdysone receptor is a synapomorphy for Mecopterida that clarifies the Strepsiptera problem,” Insect Molecular Biology, vol. 15, no. 3, pp. 351–362, 2006.
- T. Iwema, A. Chaumot, R. A. Studer et al., “Structural and evolutionary innovation of the heterodimerization interface between USP and the ecdysone receptor ECR in insects,” Molecular Biology and Evolution, vol. 26, no. 4, pp. 753–768, 2009.
- G. Aspöck, H. Kagoshima, G. Niklaus, and T. R. Bürglin, “Caenorhabditis elegans has scores of hedgehog-related genes: sequence and expression analysis,” Genome Research, vol. 9, no. 10, pp. 909–923, 1999.
- L. Hao, R. Johnsen, G. Lauter, D. Baillie, and T. R. Bürglin, “Comprehensive analysis of gene expression patterns of hedgehog-related genes,” BMC Genomics, vol. 7, article 280, 2006.
- D. A. Fitzpatrick, D. M. O'Halloran, and A. M. Burnell, “Multiple lineage specific expansions within the guanylyl cyclase gene family,” BMC Evolutionary Biology, vol. 6, article 26, p. 18, 2006.
- C. Popovici, R. Roubin, F. Coulier, P. Pontarotti, and D. Birnbaum, “The family of Caenorhabditis elegans tyrosine kinase receptors: similarities and differences with mammalian receptors,” Genome Research, vol. 9, no. 11, pp. 1026–1039, 1999.
- H. M. Robertson and J. H. Thomas, “The putative chemoreceptor families of C. elegans,” in WormBook, The C. elegans Research Community, Ed., 2006.
- A. E. Sluder, S. W. Mathews, D. Hough, V. P. Yin, and C. V. Maina, “The nuclear receptor superfamily has undergone extensive proliferation and diversification in nematodes,” Genome Research, vol. 9, no. 2, pp. 103–120, 1999.
- O. Lespinet, Y. I. Wolf, E. V. Koonin, and L. Aravind, “The role of lineage-specific gene family expansion in the evolution of eukaryotes,” Genome Research, vol. 12, no. 7, pp. 1048–1059, 2002.
- A. R. O. Cavalcanti, R. Ferreira, Z. Gu, and W. H. Li, “Patterns of gene duplication in Saccharomyces cerevisiae and Caenorhabditis elegans,” Journal of Molecular Evolution, vol. 56, no. 1, pp. 28–37, 2003.
- C. Elegans Sequencing Consortium, “Genome sequence of the nematode C. elegans: a platform for investigating biology,” Science, vol. 282, no. 5396, pp. 2012–2018, 1998.
- H. M. Robertson, “Updating the str and srj (stl) families of chemoreceptors in Caenorhabditis nematodes reveals frequent gene movement within and between chromosomes,” Chemical Senses, vol. 26, no. 2, pp. 151–159, 2001.
- L. D. Stein, Z. Bao, D. Blasiar et al., “The genome sequence of Caenorhabditis briggsae: a platform for comparative genomics,” PLoS Biology, vol. 1, no. 2, article E45, 2003.
- G. Smant, J. P. W. G. Stokkermans, Y. Yan et al., “Endogenous cellulases in animals: isolation of β-1,4-endoglucanase genes from two species of plant-parasitic cyst nematodes,” Proceedings of the National Academy of Sciences of the United States of America, vol. 95, no. 9, pp. 4906–4911, 1998.
- T. Kikuchi, J. T. Jones, T. Aikawa, H. Kosaka, and N. Ogura, “A family of glycosyl hydrolase family 45 cellulases from the pine wood nematode Bursaphelenchus xylophilus,” FEBS Letters, vol. 572, no. 1–3, pp. 201–205, 2004.
- E. G. J. Danchin, M. N. Rosso, P. Vieira et al., “Multiple lateral gene transfers and duplications have promoted plant parasitism ability in nematodes,” Proceedings of the National Academy of Sciences of the United States of America, vol. 107, no. 41, pp. 17651–17656, 2010.
- R. J. Sommer and A. Streit, “Comparative genetics and genomics of nematodes: genome structure, development, and lifestyle,” Annual Reviews of Genetics, vol. 45, pp. 1–20, 2011.
- C. Dieterich, S. W. Clifton, L. N. Schuster et al., “The Pristionchus pacificus genome provides a unique perspective on nematode lifestyle and parasitism,” Nature Genetics, vol. 40, no. 10, pp. 1193–1198, 2008.
- J. H. Thomas, J. L. Kelly, H. M. Robertson, K. Ly, and W. J. Swanson, “Adaptive evolution in the SRZ chemoreceptor families of Caenorhabditis elegans and Caenorhabditis briggsae,” Proceedings of the National Academy of Sciences of the United States of America, vol. 102, no. 12, pp. 4476–4481, 2005.
- J. C. Fay, “Weighing the evidence for adaptation at the molecular level,” Trends in Genetics, vol. 27, no. 9, pp. 343–349, 2011.
- G. Dover, “Molecular drive: a cohesive mode of species evolution,” Nature, vol. 299, no. 5879, pp. 111–117, 1982.
- G. Marais, D. Mouchiroud, and L. Duret, “Does recombination improve selection on codon usage? Lessons from nematode and fly complete genomes,” Proceedings of the National Academy of Sciences of the United States of America, vol. 98, no. 10, pp. 5688–5692, 2001.
- N. Galtier and L. Duret, “Adaptation or biased gene conversion? Extending the null hypothesis of molecular evolution,” Trends in Genetics, vol. 23, no. 6, pp. 273–277, 2007.
- M. Lynch, L.-M. Bobay, F. Catania, J.-F. Gout, and M. Rho, “The repatterning of eukaryotic genomes by random genetic drift,” Annual Reviews of Genomics and Human Genetics, vol. 12, pp. 347–366, 2011.
- F. Bonneton, A. Chaumot, and V. Laudet, “Annotation of Tribolium nuclear receptors reveals an increase in evolutionary rate of a network controlling the ecdysone cascade,” Insect Biochemistry and Molecular Biology, vol. 38, no. 4, pp. 416–429, 2008.
- G. C. Conant and K. H. Wolfe, “Turning a hobby into a job: how duplicated genes find new functions,” Nature Reviews Genetics, vol. 9, no. 12, pp. 938–950, 2008.
- R. A. Studer and M. Robinson-Rechavi, “How confident can we be that orthologs are similar, but paralogs differ?” Trends in Genetics, vol. 25, no. 5, pp. 210–216, 2009.
- R. A. Studer and M. Robinson-Rechavi, “Large-scale analysis of orthologs and paralogs under covarion-like and constant-but-different models of amino acid evolution,” Molecular Biology and Evolution, vol. 27, no. 11, pp. 2618–2627, 2010.
- M. Robinson-Rechavi, C. V. Maina, C. R. Gissendanner, V. Laudet, and A. Sluder, “Explosive lineage-specific expansion of the orphan nuclear receptor HNF4 in nematodes,” Journal of Molecular Evolution, vol. 60, no. 5, pp. 577–586, 2005.
- H. Gronemeyer, J. Å. Gustafsson, and V. Laudet, “Principles for modulation of the nuclear receptor superfamily,” Nature Reviews Drug Discovery, vol. 3, no. 11, pp. 950–964, 2004.
- J. T. Bridgham, S. M. Carroll, and J. W. Thornton, “Evolution of hormone-receptor complexity by molecular exploitation,” Science, vol. 312, no. 5770, pp. 97–101, 2006.
- S. M. Carroll, E. A. Ortlund, and J. W. Thornton, “Mechanisms for the evolution of a derived function in the ancestral glucocorticoid receptor,” PLoS Genetics, vol. 7, no. 6, Article ID e1002117, 2011.
- P. Huang, V. Chandra, and F. Rastinejad, “Structural overview of the nuclear receptor superfamily: insights into physiology and therapeutics,” Annual Review of Physiology, vol. 72, pp. 247–272, 2009.
- E. Zanaria, F. Muscatelli, B. Bardoni et al., “An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita,” Nature, vol. 372, no. 6507, pp. 635–641, 1994.
- C. S. Thummel, “Dueling orphans—interacting nuclear receptors coordinate Drosophila metamorphosis,” BioEssays, vol. 19, no. 8, pp. 669–672, 1997.
- U. Nauber, M. J. Pankratz, A. Kienlin, E. Seifert, U. Klemm, and H. Jackle, “Abdominal segmentation of the Drosophila embryo requires a hormone receptor-like protein encoded by the gap gene knirps,” Nature, vol. 336, no. 6198, pp. 489–492, 1988.
- M. Gonzalez-Gaitan, M. Rothe, E. A. Wimmer, H. Taubert, and H. Jackle, “Redundant functions of the genes knirps and knirps-related for the establishment of anterior Drosophila head structures,” Proceedings of the National Academy of Sciences of the United States of America, vol. 91, no. 18, pp. 8567–8571, 1994.
- M. Rothe, M. Pehl, H. Taubert, and H. Jackle, “Loss of gene function through rapid mitotic cycles in the Drosophila embryo,” Nature, vol. 359, no. 6391, pp. 156–159, 1992.
- A. C. Cerny, D. Grossmann, G. Bucher, and M. Klingler, “The Tribolium ortholog of knirps and knirps-related is crucial for head segmentation but plays a minor role during abdominal patterning,” Developmental Biology, vol. 321, no. 1, pp. 284–294, 2008.
- E. Morán and G. Jiménez, “The tailless nuclear receptor acts as a dedicated repressor in the early Drosophila embryo,” Molecular and Cellular Biology, vol. 26, no. 9, pp. 3446–3454, 2006.
- M. J. Wilson and P. K. Dearden, “Tailless patterning functions are conserved in the honeybee even in the absence of Torso signaling,” Developmental Biology, vol. 335, no. 1, pp. 276–287, 2009.
- K. M. Rudolph, G. J. Liaw, A. Daniel et al., “Complex regulatory region mediating tailless expression in early embryonic patterning and brain development,” Development, vol. 124, no. 21, pp. 4297–4308, 1997.
- H. Gui, M. L. Li, and C. C. Tsai, “A tale of tailless,” Developmental Neuroscience, vol. 33, no. 1, pp. 1–13, 2011.
- J. S. Fernandes and P. W. Sternberg, “The tailless ortholog nhr-67 regulates patterning of gene expression and morphogenesis in the C. elegans vulva,” PLoS Genetics, vol. 3, no. 4, article e69, 2007.
- M. Kato and P. W. Sternberg, “The C. elegans tailless/Tlx homolog nhr-67 regulates a stage-specific program of linker cell migration in male gonadogenesis,” Development, vol. 136, no. 23, pp. 3907–3915, 2009.
- X. Wang and R. J. Sommer, “Antagonism of LIN-17/frizzled and LIN-18/RyK in nematode vulva induction reveals evolutionary alterations in core developmental pathways,” PLoS Biology, vol. 9, no. 7, Article ID e1001110, 2011.
- H. E. Hoekstra and J. A. Coyne, “The locus of evolution: evo devo and the genetics of adaptation,” Evolution, vol. 61, no. 5, pp. 995–1016, 2007.
- S. B. Carroll, “Evo-devo and an expanding evolutionary synthesis: a genetic theory of morphological evolution,” Cell, vol. 134, no. 1, pp. 25–36, 2008.
- D. L. Stern and V. Orgogozo, “The loci of evolution: how predictable is genetic evolution?” Evolution, vol. 62, no. 9, pp. 2155–2177, 2008.
- G. J. Liaw and J. A. Lengyel, “Control of tailless expression by bicoid, dorsal and synergistically interacting terminal system regulatory elements,” Mechanisms of Development, vol. 40, no. 1-2, pp. 47–61, 1992.
- G. J. Liaw, K. M. Rudolph, J. D. Huang, T. Dubnicoff, A. J. Courey, and J. A. Lengyel, “The torso response element binds GAGA and NTF-1/Elf-1, and regulates tailless by relief of repression,” Genes and Development, vol. 9, no. 24, pp. 3163–3176, 1995.
- R. Sommer and D. Tautz, “Segmentation gene expression in the housefly Musca domestica,” Development, vol. 113, no. 2, pp. 419–430, 1991.
- N. S. Wratten, A. P. McGregor, P. J. Shaw, and G. A. Dover, “Evolutionary and functional analysis of the tailless enhancer in Musca domestica and Drosophila melanogaster,” Evolution and Development, vol. 8, no. 1, pp. 6–15, 2006.
- M. Schoppmeier and R. Schröder, “Maternal torso signaling controls body axis elongation in a short germ insect,” Current Biology, vol. 15, no. 23, pp. 2131–2136, 2005.
- J. A. Lynch, E. C. Olesnicky, and C. Desplan, “Regulation and function of tailless in the long germ wasp Nasonia vitripennis,” Development Genes and Evolution, vol. 216, no. 7-8, pp. 493–498, 2006.
- R. Schröder, “The genes orthodenticle and hunchback substitute for bicoid in the beetle Tribolium,” Nature, vol. 422, no. 6932, pp. 621–625, 2003.
- M. T. Weirauch and T. R. Hughes, “Conserved expression without conserved regulatory sequence: the more things change, the more they stay the same,” Trends in Genetics, vol. 26, no. 2, pp. 66–74, 2010.
- J. R. True and E. S. Haag, “Developmental system drift and flexibility in evolutionary trajectories,” Evolution and Development, vol. 3, no. 2, pp. 109–119, 2001.
- C. Darwin, The Autobiography of Charles Darwin 1809–1882, With Original Omissions Restored, Edited With Appendix and Notes by Nora Barlow, Harcourt, Brace & Co., New York, NY, USA, 1959.
- G. P. Wagner, “The developmental genetics of homology,” Nature Reviews Genetics, vol. 8, no. 6, pp. 473–479, 2007.