甲壳类动物海陆过渡后,鳃的渗透调节进化促进了盐度适应。

IF 5.8 2区 生物学 Q1 MARINE & FRESHWATER BIOLOGY
Marine Life Science & Technology Pub Date : 2025-05-15 eCollection Date: 2025-05-01 DOI:10.1007/s42995-025-00298-6
Hongguang Liu, Xiaokun Wang, Zeyu Liu, Shuqiang Li, Zhonge Hou
{"title":"甲壳类动物海陆过渡后,鳃的渗透调节进化促进了盐度适应。","authors":"Hongguang Liu, Xiaokun Wang, Zeyu Liu, Shuqiang Li, Zhonge Hou","doi":"10.1007/s42995-025-00298-6","DOIUrl":null,"url":null,"abstract":"<p><p>The sea-land transition is one of the most dramatic evolutionary changes and requires an adaptive genetic response to salinity changes and osmotic stress. Here, we used multi-species genomes and multi-tissue transcriptomes of the talitrid crustaceans, a living sea-land transition model, to investigate the adaptive genetic changes and osmoregulatory organs that facilitated their salinity adaptation. Genomic analyses detected numerous osmoregulatory genes in terrestrial talitrids undergoing gene family expansions and positive selection. Gene expression comparisons among species and tissues confirmed the gill being the primary organ responsible for ion transport and identified the genetic expression variation that enable talitrids to adapt to marine and land habitats. V-type H<sup>+</sup>-ATPases related to H<sup>+</sup> transport play a crucial role in land adaptations, while genes related to the transport of inorganic ions (Na<sup>+</sup>, K<sup>+</sup>, Cl<sup>-</sup>) are upregulated in marine habitats. Our results demonstrate that talitrids have divergent genetic responses to salinity change that led to the uptake or excretion of ions in the gills and promoted habitat adaptation. These findings suggest that detecting gene expression changes in talitrids presents promising potential as a biomarker for salinity monitoring.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s42995-025-00298-6.</p>","PeriodicalId":53218,"journal":{"name":"Marine Life Science & Technology","volume":"7 2","pages":"205-217"},"PeriodicalIF":5.8000,"publicationDate":"2025-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12102416/pdf/","citationCount":"0","resultStr":"{\"title\":\"Osmoregulatory evolution of gills promoted salinity adaptation following the sea-land transition of crustaceans.\",\"authors\":\"Hongguang Liu, Xiaokun Wang, Zeyu Liu, Shuqiang Li, Zhonge Hou\",\"doi\":\"10.1007/s42995-025-00298-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The sea-land transition is one of the most dramatic evolutionary changes and requires an adaptive genetic response to salinity changes and osmotic stress. Here, we used multi-species genomes and multi-tissue transcriptomes of the talitrid crustaceans, a living sea-land transition model, to investigate the adaptive genetic changes and osmoregulatory organs that facilitated their salinity adaptation. Genomic analyses detected numerous osmoregulatory genes in terrestrial talitrids undergoing gene family expansions and positive selection. Gene expression comparisons among species and tissues confirmed the gill being the primary organ responsible for ion transport and identified the genetic expression variation that enable talitrids to adapt to marine and land habitats. V-type H<sup>+</sup>-ATPases related to H<sup>+</sup> transport play a crucial role in land adaptations, while genes related to the transport of inorganic ions (Na<sup>+</sup>, K<sup>+</sup>, Cl<sup>-</sup>) are upregulated in marine habitats. Our results demonstrate that talitrids have divergent genetic responses to salinity change that led to the uptake or excretion of ions in the gills and promoted habitat adaptation. These findings suggest that detecting gene expression changes in talitrids presents promising potential as a biomarker for salinity monitoring.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s42995-025-00298-6.</p>\",\"PeriodicalId\":53218,\"journal\":{\"name\":\"Marine Life Science & Technology\",\"volume\":\"7 2\",\"pages\":\"205-217\"},\"PeriodicalIF\":5.8000,\"publicationDate\":\"2025-05-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12102416/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Marine Life Science & Technology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1007/s42995-025-00298-6\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/5/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q1\",\"JCRName\":\"MARINE & FRESHWATER BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Marine Life Science & Technology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s42995-025-00298-6","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/5/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"MARINE & FRESHWATER BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

海陆过渡是最剧烈的进化变化之一,需要对盐度变化和渗透胁迫作出适应性的遗传反应。本研究利用海陆转换模式的多物种基因组和多组织转录组,研究了促进其盐度适应的适应性遗传变化和渗透调节器官。基因组分析检测到许多渗透调节基因在经历基因家族扩展和积极选择的陆生海藻。物种和组织之间的基因表达比较证实了鳃是负责离子运输的主要器官,并确定了使鳍鱼适应海洋和陆地栖息地的遗传表达变异。与H+转运相关的v型H+- atp酶在陆地适应中起着至关重要的作用,而与无机离子(Na+, K+, Cl-)转运相关的基因在海洋栖息地中上调。我们的研究结果表明,海藻对盐度变化有不同的遗传反应,导致鳃吸收或排泄离子,促进栖息地适应。这些发现表明,检测盐盐中基因表达的变化作为盐度监测的生物标志物具有很大的潜力。补充信息:在线版本包含补充资料,可在10.1007/s42995-025-00298-6获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Osmoregulatory evolution of gills promoted salinity adaptation following the sea-land transition of crustaceans.

The sea-land transition is one of the most dramatic evolutionary changes and requires an adaptive genetic response to salinity changes and osmotic stress. Here, we used multi-species genomes and multi-tissue transcriptomes of the talitrid crustaceans, a living sea-land transition model, to investigate the adaptive genetic changes and osmoregulatory organs that facilitated their salinity adaptation. Genomic analyses detected numerous osmoregulatory genes in terrestrial talitrids undergoing gene family expansions and positive selection. Gene expression comparisons among species and tissues confirmed the gill being the primary organ responsible for ion transport and identified the genetic expression variation that enable talitrids to adapt to marine and land habitats. V-type H+-ATPases related to H+ transport play a crucial role in land adaptations, while genes related to the transport of inorganic ions (Na+, K+, Cl-) are upregulated in marine habitats. Our results demonstrate that talitrids have divergent genetic responses to salinity change that led to the uptake or excretion of ions in the gills and promoted habitat adaptation. These findings suggest that detecting gene expression changes in talitrids presents promising potential as a biomarker for salinity monitoring.

Supplementary information: The online version contains supplementary material available at 10.1007/s42995-025-00298-6.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Marine Life Science & Technology
Marine Life Science & Technology MARINE & FRESHWATER BIOLOGY-
CiteScore
9.60
自引率
10.50%
发文量
58
期刊介绍: Marine Life Science & Technology (MLST), established in 2019, is dedicated to publishing original research papers that unveil new discoveries and theories spanning a wide spectrum of life sciences and technologies. This includes fundamental biology, fisheries science and technology, medicinal bioresources, food science, biotechnology, ecology, and environmental biology, with a particular focus on marine habitats. The journal is committed to nurturing synergistic interactions among these diverse disciplines, striving to advance multidisciplinary approaches within the scientific field. It caters to a readership comprising biological scientists, aquaculture researchers, marine technologists, biological oceanographers, and ecologists.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信