盐度普通生物对低盐压力的不同反应为硅藻在淡水中的定殖提供了启示。

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Ecology Pub Date : 2024-10-21 DOI:10.1111/mec.17556
Kathryn J. Judy, Eveline Pinseel, Kala M. Downey, Jeffrey A. Lewis, Andrew J. Alverson
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引用次数: 0

摘要

环境转变(如海水和淡水之间的盐度分界线)在浅层和深层时间尺度上塑造了生物多样性,开辟了新的生态位,为加速物种演化和适应性辐射创造了机会。了解环境适应的遗传学是理解生物如何在新的栖息地定居并随后实现多样化的核心。我们利用时间分辨转录组学对比了两种硅藻的低盐度应激反应。Skeletonema marinoi具有深海祖先,但最近侵入了咸水。Cyclotella cryptica具有深层淡水的血统,能承受的盐度范围更广。与隐杆线虫相比,海鞘在缓解轻度盐度胁迫方面的能力较弱,而隐杆线虫具有独特的机制,可迅速缓解低盐度胁迫并在低盐度环境中长期生长。我们的研究表明,低盐度耐受性的细胞机制使硅藻在全球淡水栖息地中实现了多样化,其中包括在整个硅藻系中既保守又可变的元素。浮游植物中祖先和品系特有的环境响应之间的平衡在进化时间尺度上决定了海洋-淡水的过渡,而在当代时间尺度上,将影响哪些品系生存下来并适应不断变化的海洋条件。
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The Divergent Responses of Salinity Generalists to Hyposaline Stress Provide Insights Into the Colonisation of Freshwaters by Diatoms

Environmental transitions, such as the salinity divide separating marine and fresh waters, shape biodiversity over both shallow and deep timescales, opening up new niches and creating opportunities for accelerated speciation and adaptive radiation. Understanding the genetics of environmental adaptation is central to understanding how organisms colonise and subsequently diversify in new habitats. We used time-resolved transcriptomics to contrast the hyposalinity stress responses of two diatoms. Skeletonema marinoi has deep marine ancestry but has recently invaded brackish waters. Cyclotella cryptica has deep freshwater ancestry and can withstand a much broader salinity range. Skeletonema marinoi is less adept at mitigating even mild salinity stress compared to Cyclotella cryptica, which has distinct mechanisms for rapid mitigation of hyposaline stress and long-term growth in low salinity. We show that the cellular mechanisms underlying low salinity tolerance, which has allowed diversification across freshwater habitats worldwide, includes elements that are both conserved and variable across the diatom lineage. The balance between ancestral and lineage-specific environmental responses in phytoplankton have shaped marine–freshwater transitions on evolutionary timescales and, on contemporary timescales, will affect which lineages survive and adapt to changing ocean conditions.

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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
期刊最新文献
Population Genetics and Invasion History of the European Starling Across Aotearoa New Zealand. An Early-Life Disruption of Gut Microbiota Has Opposing Effects on Parasite Resistance in Two Host Species. Genetic Monitoring of a Lethal Control Programme for Wild Canids With Complex Mating Strategies. Elevational Range Impacts Connectivity and Predicted Deme Sizes From Models of Habitat Suitability. Michael C. Whitlock-Recipient of the 2024 Molecular Ecology Prize.
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