Pseudo-chromosome–length genome assembly for a deep-sea eel Ilyophis brunneus sheds light on the deep-sea adaptation

被引:0
|
作者
Jie Chen [1 ,2 ]
Honghui Zeng [3 ]
Wenqi Lv [3 ,2 ]
Ning Sun [3 ,2 ]
Cheng Wang [3 ,2 ]
Wenjie Xu [4 ]
Mingliang Hu [4 ]
Xiaoni Gan [3 ]
Lisheng He [1 ,2 ]
Shunping He [1 ,3 ]
Chengchi Fang [3 ,2 ]
机构
[1] Institute of Deep-Sea Science and Engineering,Chinese Academy of Sciences
[2] University of Chinese Academy of Sciences
[3] State Key Laboratory of Freshwater Ecology and Biotechnology,Institute of Hydrobiology,Chinese Academy of Sciences
[4] School for Ecological and Environmental Sciences,Northwestern Polytechnical University
基金
中国国家自然科学基金;
关键词
D O I
暂无
中图分类号
Q953 [动物遗传学];
学科分类号
071007 ; 090501 ;
摘要
High hydrostatic pressure,low temperature,and scarce food supply are the major factors that limit the survival of vertebrates in extreme deep-sea environments.Here,we constructed a high-quality genome of the deep-sea Muddy arrowtooth eel(MAE,Ilyophis brunneus,captured below a depth of 3,500 m) by using Illumina,Pac Bio,and Hi-C sequencing.We compare it against those of shallow-water eel and other outgroups to explore the genetic basis that underlies the adaptive evolution to deep-sea biomes.The MAE genome was estimated to be 1.47 Gb and assembled into 14 pseudo-chromosomes.Phylogenetic analyses indicated that MAE diverged from its closely related shallow-sea species,European eel,~111.9 Mya and experienced a rapid evolution.The genome evolutionary analyses primarily revealed the following:(i) under high hydrostatic pressure,the positively selected gene TUBGCP3 and the expanded family MLC1 may improve the cytoskeleton stability; ACOX1 may enhance the fluidity of cell membrane and maintain transport activity; the expansion of ABCC12 gene family may enhance the integrity of DNA;(ii) positively selected HARS likely maintain the transcription ability at low temperatures; and(iii) energy metabolism under a food-limited environment may be increased by expanded and positively selected genes in AMPK and m TOR signaling pathways.
引用
收藏
页码:1379 / 1391
页数:13
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