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基础脊椎动物阐明了与纤毛病相关基因 Tmem138 和 Tmem216 相关的进化史。

Basal vertebrates clarify the evolutionary history of ciliopathy-associated genes Tmem138 and Tmem216.

机构信息

Comparative Genomics Lab, Institute of Molecular and Cell Biology, A*STAR, Biopolis, Singapore.

出版信息

Mol Biol Evol. 2013 Jan;30(1):62-5. doi: 10.1093/molbev/mss215. Epub 2012 Aug 30.

Abstract

Recently, Lee et al. (Lee JH, Silhavy JL, Lee JE, et al. (30 co-authors). 2012. Evolutionarily assembled cis-regulatory module at a human ciliopathy locus. Science (335:966-969.) demonstrated that mutation in either of the transmembrane protein encoding genes, TMEM138 or TMEM216, causes phenotypically indistinguishable ciliopathy. Furthermore, on the basis of the observation that their orthologs are linked in a head-to-tail configuration in other mammals and Anolis, but present on different scaffolds or chromosomes in Xenopus tropicalis and zebrafish, the authors concluded that the two genes were joined by chromosomal rearrangement at the evolutionary amphibian-to-reptile transition to form a functional module. We have sequenced these gene loci in a cartilaginous fish, the elephant shark, and found that the two genes together with a related gene (Tmem80) constitute a tandem cluster. This suggests that the two genes were already linked in the vertebrate ancestor and then rearranged independently in Xenopus and zebrafish. Analyses of the coelacanth and lamprey genomes support this hypothesis. Our study highlights the importance of basal vertebrates as critical reference genomes.

摘要

最近,Lee 等人(Lee JH、Silhavy JL、Lee JE 等 30 位共同作者)。2012. 人类纤毛病相关基因座上的进化组装顺式调控模块。科学(335:966-969)。表明,跨膜蛋白编码基因 TMEM138 或 TMEM216 中的任何一个突变都会导致表型上无法区分的纤毛病。此外,基于它们的同源物在其他哺乳动物和 Anolis 中以头尾相连的方式连接的观察结果,但在 Xenopus tropicalis 和斑马鱼中位于不同的支架或染色体上,作者得出结论,这两个基因在进化的两栖动物到爬行动物过渡过程中通过染色体重排连接在一起,形成了一个功能模块。我们在软骨鱼类,即象鲨中对这些基因座进行了测序,发现这两个基因与一个相关基因(Tmem80)一起构成了串联簇。这表明这两个基因在脊椎动物祖先中已经连接在一起,然后在 Xenopus 和斑马鱼中独立重排。对腔棘鱼和七鳃鳗基因组的分析支持这一假设。我们的研究强调了基础脊椎动物作为关键参考基因组的重要性。

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