Author
Listed:
- Wei Yin
(Zhongshan School of Medicine, Sun Yat-sen University)
- Zong-ji Wang
(Life Sciences Institute, The Key Laboratory of Conservation Biology for Endangered Wildlife of the Ministry of Education, Zhejiang University
China National Genebank, BGI-Shenzhen
State Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences
School of Bioscience & Bioengineering, South China University of Technology)
- Qi-ye Li
(China National Genebank, BGI-Shenzhen
State Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences
Centre for GeoGenetics, Natural History Museum of Denmark, University of Copenhagen)
- Jin-ming Lian
(China National Genebank, BGI-Shenzhen)
- Yang Zhou
(China National Genebank, BGI-Shenzhen)
- Bing-zheng Lu
(Zhongshan School of Medicine, Sun Yat-sen University)
- Li-jun Jin
(China National Genebank, BGI-Shenzhen)
- Peng-xin Qiu
(Zhongshan School of Medicine, Sun Yat-sen University)
- Pei Zhang
(China National Genebank, BGI-Shenzhen)
- Wen-bo Zhu
(Zhongshan School of Medicine, Sun Yat-sen University)
- Bo Wen
(BGI-Shenzhen)
- Yi-jun Huang
(Zhongshan School of Medicine, Sun Yat-sen University)
- Zhi-long Lin
(BGI-Shenzhen)
- Bi-tao Qiu
(China National Genebank, BGI-Shenzhen
Centre for Social Evolution, University of Copenhagen)
- Xing-wen Su
(Zhongshan School of Medicine, Sun Yat-sen University)
- Huan-ming Yang
(BGI-Shenzhen
James D. Watson Institute of Genome Sciences)
- Guo-jie Zhang
(China National Genebank, BGI-Shenzhen
State Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences
Centre for Social Evolution, University of Copenhagen)
- Guang-mei Yan
(Zhongshan School of Medicine, Sun Yat-sen University)
- Qi Zhou
(Life Sciences Institute, The Key Laboratory of Conservation Biology for Endangered Wildlife of the Ministry of Education, Zhejiang University
University of California, Berkeley)
Abstract
Snakes have numerous features distinctive from other tetrapods and a rich history of genome evolution that is still obscure. Here, we report the high-quality genome of the five-pacer viper, Deinagkistrodon acutus, and comparative analyses with other representative snake and lizard genomes. We map the evolutionary trajectories of transposable elements (TEs), developmental genes and sex chromosomes onto the snake phylogeny. TEs exhibit dynamic lineage-specific expansion, and many viper TEs show brain-specific gene expression along with their nearby genes. We detect signatures of adaptive evolution in olfactory, venom and thermal-sensing genes and also functional degeneration of genes associated with vision and hearing. Lineage-specific relaxation of functional constraints on respective Hox and Tbx limb-patterning genes supports fossil evidence for a successive loss of forelimbs then hindlimbs during snake evolution. Finally, we infer that the ZW sex chromosome pair had undergone at least three recombination suppression events in the ancestor of advanced snakes. These results altogether forge a framework for our deep understanding into snakes’ history of molecular evolution.
Suggested Citation
Wei Yin & Zong-ji Wang & Qi-ye Li & Jin-ming Lian & Yang Zhou & Bing-zheng Lu & Li-jun Jin & Peng-xin Qiu & Pei Zhang & Wen-bo Zhu & Bo Wen & Yi-jun Huang & Zhi-long Lin & Bi-tao Qiu & Xing-wen Su & H, 2016.
"Evolutionary trajectories of snake genes and genomes revealed by comparative analyses of five-pacer viper,"
Nature Communications, Nature, vol. 7(1), pages 1-11, December.
Handle:
RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms13107
DOI: 10.1038/ncomms13107
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