渗透调节基因定向选择对鼻蝽淡水适应的适应性进化。

IF 3.9 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Shuang Han, Jie Wang, Taixing Lin, Jingping Zhang, Adelino V M Canario, Qigen Liu, Liangbiao Chen
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引用次数: 0

摘要

海洋鱼类适应淡水生境的分子机制尚不清楚。弹尾凤尾鱼,如Coilia nasus,起源于海洋环境,包括溯河和淡水居住的同种鱼,使它们成为研究从海洋到淡水栖息地适应进化的理想选择。本文对来自长江干流和河口地区的两个不同的鼻窦猿谱系进行了比较种群基因组和转录组分析,其中一个是溯河种群,另一个是淡水种群。通过对溯河种群和淡水种群的全基因组基因分型,我们观察到与生态适应和迁移能量消耗相关的渗透调节、能量代谢和免疫反应途径存在显著差异。一些离子转运基因如CAMK1、ATP1α3、KCNJ1和SLC30A2可能有助于淡水适应。值得注意的是,许多矿物皮质激素信号基因(如NR3C2、SGK1、ATP1α3、KCNJ1)在咸水种群和淡水种群之间表现出动态变化,表明激素皮质醇在调节盐盐鱼类的盐度适应中起重要作用。在这些基因中,离子通道ATP1α3经历了适应性氨基酸替换(Val317Ile和Thr329Ser),根据同源性比较,这似乎是迁徙物种的进化热点。这些变异可能促进钠/钾运输,并强调盐度耐受性是溯河鱼类向淡水过渡的关键驱动因素。这些结果增强了我们对溯河鱼类跨渗透边界适应淡水的遗传基础的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adaptive Evolution for Freshwater Adaptation in Coilia nasus by Directional Selection on Osmoregulation Genes.

The molecular mechanisms underlying the adaptation to freshwater habitats in fish of marine origin remain unclear. Grenadier anchovies, such as Coilia nasus, originate from marine environments and include both anadromous and freshwater-resident conspecifics, making them ideal for studying adaptive evolution from marine to freshwater habitats. We conducted a comparative population genomic and transcriptome analysis of two distinct C. nasus lineages, one anadromous and the other freshwater-resident, collected from mainstream and estuarine regions of the Yangtze River, China. By genome-wide genotyping of the anadromous and the freshwater-resident populations, we observed significant divergence in osmoregulation, energy metabolism, and immune response pathways associated with ecological adaptation and energy expenditure for migration. Some ion transport genes such as CAMK1, ATP1α3, KCNJ1 and SLC30A2 were identified that may contribute to freshwater adaptation. Notably, numerous mineralocorticoid signalling genes (e.g., NR3C2, SGK1, ATP1α3, KCNJ1) exhibit dynamic change between the anadromous and freshwater populations, suggesting an important role for the hormone cortisol in regulating salinity acclimation in euryhaline fish. Among these genes, the ion channel ATP1α3 experienced adaptive amino acid substitutions (Val317Ile and Thr329Ser), which appear to be evolutionary hotspots across migratory species based on ortholog comparisons. These variants may facilitate sodium/potassium transport and highlight salinity tolerance as a key driver of divergence in anadromous fish transitioning to freshwater. These results enhance our understanding of the genetic basis underlying freshwater adaptation for an anadromous fish across osmotic boundaries.

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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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