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洞穴鱼基因组揭示了导致眼睛退化的候选基因。

The cavefish genome reveals candidate genes for eye loss.

作者信息

McGaugh Suzanne E, Gross Joshua B, Aken Bronwen, Blin Maryline, Borowsky Richard, Chalopin Domitille, Hinaux Hélène, Jeffery William R, Keene Alex, Ma Li, Minx Patrick, Murphy Daniel, O'Quin Kelly E, Rétaux Sylvie, Rohner Nicolas, Searle Steve M J, Stahl Bethany A, Tabin Cliff, Volff Jean-Nicolas, Yoshizawa Masato, Warren Wesley C

机构信息

The Genome Institute, Washington University, Campus Box 8501, St Louis, Missouri 63108, USA.

Department of Biological Sciences, University of Cincinnati, 711B Rieveschl Hall, 312 College Drive, Cincinnati, Ohio 45221, USA.

出版信息

Nat Commun. 2014 Oct 20;5:5307. doi: 10.1038/ncomms6307.

Abstract

Natural populations subjected to strong environmental selection pressures offer a window into the genetic underpinnings of evolutionary change. Cavefish populations, Astyanax mexicanus (Teleostei: Characiphysi), exhibit repeated, independent evolution for a variety of traits including eye degeneration, pigment loss, increased size and number of taste buds and mechanosensory organs, and shifts in many behavioural traits. Surface and cave forms are interfertile making this system amenable to genetic interrogation; however, lack of a reference genome has hampered efforts to identify genes responsible for changes in cave forms of A. mexicanus. Here we present the first de novo genome assembly for Astyanax mexicanus cavefish, contrast repeat elements to other teleost genomes, identify candidate genes underlying quantitative trait loci (QTL), and assay these candidate genes for potential functional and expression differences. We expect the cavefish genome to advance understanding of the evolutionary process, as well as, analogous human disease including retinal dysfunction.

摘要

受到强大环境选择压力的自然种群为了解进化变化的遗传基础提供了一个窗口。洞穴鱼种群,即墨西哥丽脂鲤(硬骨鱼纲:脂鲤科),在包括眼睛退化、色素丧失、味蕾和机械感觉器官的大小和数量增加以及许多行为特征的转变等多种性状上表现出反复、独立的进化。表层和洞穴形态的鱼可以杂交,这使得该系统适合进行遗传研究;然而,缺乏参考基因组阻碍了人们识别负责墨西哥丽脂鲤洞穴形态变化的基因的努力。在这里,我们展示了首个墨西哥丽脂鲤洞穴鱼的从头基因组组装,将重复元件与其他硬骨鱼基因组进行对比,识别数量性状位点(QTL)潜在的候选基因,并分析这些候选基因的潜在功能和表达差异。我们期望洞穴鱼基因组能够促进对进化过程的理解,以及对包括视网膜功能障碍在内的类似人类疾病的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce01/4218959/8fbbc2aa0a5f/ncomms6307-f1.jpg

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