The genome and transcriptome of Japanese flounder provide insights into flatfish asymmetry

Changwei Shao(Qingdao National Laboratory for Marine Science and Technology), Baolong Bao(Shanghai Ocean University), Zhiyuan Xie(BGI Group (China)), Xinye Chen(Shanghai Ocean University), Bo Li(BGI Group (China)), Xiaodong Jia(Qingdao National Laboratory for Marine Science and Technology), Qiulin Yao(BGI Group (China)), Guillermo Ortı́(George Washington University), Wenhui Li(BGI Group (China)), Xihong Li(Qingdao National Laboratory for Marine Science and Technology), Kristin Hamre(University of Bergen), Juan Xu(Shanghai Ocean University), Lei Wang(Qingdao National Laboratory for Marine Science and Technology), Fangyuan Chen(BGI Group (China)), Yongsheng Tian(Qingdao National Laboratory for Marine Science and Technology), A Schreiber(St. Lawrence University), Na Wang(Qingdao National Laboratory for Marine Science and Technology), Fen Wei(Shanghai Ocean University), Jilin Zhang(BGI Group (China)), Zhongdian Dong(Qingdao National Laboratory for Marine Science and Technology), Lei Gao(Shanghai Ocean University), Junwei Gai(Shanghai Ocean University), Takashi Sakamoto(Tokyo University of Marine Science and Technology), Sudong Mo(Qingdao National Laboratory for Marine Science and Technology), Wenjun Chen(Shanghai Ocean University), Qiong Shi(BGI Group (China)), Hui Li(Shanghai Ocean University), Yunji Xiu(Qingdao National Laboratory for Marine Science and Technology), Yangzhen Li(Qingdao National Laboratory for Marine Science and Technology), Wenteng Xu(Qingdao National Laboratory for Marine Science and Technology), Zhiyi Shi(Shanghai Ocean University), Guojie Zhang(BGI Group (China)), Deborah M. Power(Shanghai Ocean University), Qingyin Wang(Qingdao National Laboratory for Marine Science and Technology), Manfred Schartl(University of Würzburg), Songlin Chen(Qingdao National Laboratory for Marine Science and Technology)
Nature Genetics
December 5, 2016
Cited by 247Open Access
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Abstract

Songlin Chen, Manfred Schartl, Qingyin Wang, Deborah M. Power and colleagues analyze the genome of the Japanese flounder and its transcriptome dynamics during metamorphosis. They report a role for thyroid hormone and retinoic acid signaling, as well as phototransduction pathways, in the regulation of craniofacial asymmetry. Flatfish have the most extreme asymmetric body morphology of vertebrates. During metamorphosis, one eye migrates to the contralateral side of the skull, and this migration is accompanied by extensive craniofacial transformations and simultaneous development of lopsided body pigmentation1,2,3,4,5. The evolution of this developmental and physiological innovation remains enigmatic. Comparative genomics of two flatfish and transcriptomic analyses during metamorphosis point to a role for thyroid hormone and retinoic acid signaling, as well as phototransduction pathways. We demonstrate that retinoic acid is critical in establishing asymmetric pigmentation and, via cross-talk with thyroid hormones, in modulating eye migration. The unexpected expression of the visual opsins from the phototransduction pathway in the skin translates illumination differences and generates retinoic acid gradients that underlie the generation of asymmetry. Identifying the genetic underpinning of this unique developmental process answers long-standing questions about the evolutionary origin of asymmetry, but it also provides insight into the mechanisms that control body shape in vertebrates.


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