Chromosome-level Genome Assembly of the Small Snakehead (Channa asiatica) Provides Insights into the Genetic Basis for its Pelvic Fin Loss.

IF 2.2 2区 生物学 Q2 EVOLUTIONARY BIOLOGY
Minmin Xie, Mingpeng Zheng, Yixuan Chen, Pinpin Zhang, Zhongyi Wang, Zhaobin Song, Yi Liu, Chuang Zhou
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Abstract

The paired appendages of vertebrates are a pivotal developmental innovation, of which the pelvic fins of teleosts are evolutionarily homologous to the hind limbs of tetrapods. The small snakehead (Channa asiatica), an important freshwater fish with significant commercial value, lacks the pelvic fins while some other fish species in the same genus have. To determine the genetic changes underlying the pelvic fin loss in the small snakehead, we assembled the chromosome-level genome of the species based on PacBio HiFi and Hi-C sequencing technology and performed comparative genomics analyses. The final genome assembly of the small snakehead has a total length of 714.57 Mb with 23 chromosomes (contig N50 of 27.93 Mb and scaffold N50 of 28.54 Mb), and 193.09 Mb (27.02%) interspersed repeats and 22,300 protein-coding genes were annotated. Phylogenetic and divergence analyses indicated that the small snakehead was the sister branch to the combination of the northern snakehead (C. argus) and the blotched snakehead (C. maculata) and diverged from the common ancestor approximately 24.7 Mya. Three small snakehead-specific missense mutations were identified in tbx4 gene whose loss could cause the pelvic fin loss. Significant chromosomal rearrangement and 214 small snakehead-specific structural variations (SSSVs) were detected between the small snakehead and other Channa species. Among these SSSVs, the deletion in pax7a was likely to play a role in the pelvic fin loss. Furthermore, the specific loss of conserved non-coding regulatory elements (CNEs) related to limb/fin development was detected in the small snakehead, which possibly led to the pelvic fin loss of the small snakehead. The present study generated the high-quality chromosome-scale reference genome of the small snakehead, which provided a valuable genomic resource for the follow-up studies, and our findings shed light on the important genetic clues regarding pelvic fin loss in the species.

小黑鱼(Channa asiatica)染色体水平的基因组组装为其骨盆鳍丧失的遗传基础提供了见解。
脊椎动物的成对附属物是一种关键的发育创新,其中硬骨鱼的腹鳍在进化上与四足动物的后肢是同源的。小黑鱼是一种重要的淡水鱼,具有重要的商业价值,它没有腹鳍,而同属的其他一些鱼类却有。为了确定小蛇头骨盆鳍丢失的遗传变化,我们基于PacBio HiFi和Hi-C测序技术组装了该物种的染色体水平基因组,并进行了比较基因组学分析。小蛇头的最终基因组组装总长度为714.57 Mb,有23条染色体(contig N50为27.93 Mb, scaffold N50为28.54 Mb),有193.09 Mb(27.02%)的重复序列,有22,300个蛋白质编码基因被注释。系统发育和分化分析表明,小蛇头是北方蛇头(C. argus)和斑点蛇头(C. maculata)组合的姐妹分支,大约在24.7万年左右从共同祖先分化而来。在tbx4基因中发现了3个小的蛇头特异性错义突变,其缺失可导致腹鳍缺失。小蛇头与中国其他种类的小蛇头存在显著的染色体重排和214个小蛇头特异性结构变异(SSSVs)。在这些sssv中,pax7a的缺失可能在骨盆鳍丢失中起作用。此外,在小蛇头中检测到与肢体/鳍发育相关的保守非编码调控元件(CNEs)的特异性缺失,这可能导致小蛇头的盆鳍缺失。本研究获得了高质量的小蛇头染色体尺度参考基因组,为后续研究提供了有价值的基因组资源,并为该物种盆鳍丢失提供了重要的遗传线索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Heredity
Journal of Heredity 生物-遗传学
CiteScore
5.20
自引率
6.50%
发文量
63
审稿时长
6-12 weeks
期刊介绍: Over the last 100 years, the Journal of Heredity has established and maintained a tradition of scholarly excellence in the publication of genetics research. Virtually every major figure in the field has contributed to the journal. Established in 1903, Journal of Heredity covers organismal genetics across a wide range of disciplines and taxa. Articles include such rapidly advancing fields as conservation genetics of endangered species, population structure and phylogeography, molecular evolution and speciation, molecular genetics of disease resistance in plants and animals, genetic biodiversity and relevant computer programs.
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