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潮间带环境对太平洋牡蛎生理表型和 DNA 甲基化的跨代影响。

Transgenerational effects of intertidal environment on physiological phenotypes and DNA methylation in Pacific oysters.

机构信息

CAS and Shandong Province Key Laboratory of Experimental Marine Biology, Center for Ocean Mega-Science, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China; Laboratory for Marine Fisheries Science and Food Production Processes, Pilot National Laboratory for Marine Science and Technology, Qingdao 266237, China; National and Local Joint Engineering Laboratory of Ecological Mariculture, Qingdao 266071, China.

CAS and Shandong Province Key Laboratory of Experimental Marine Biology, Center for Ocean Mega-Science, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China; Laboratory for Marine Biology and Biotechnology, Pilot National Laboratory for Marine Science and Technology, Qingdao 266237, China; National and Local Joint Engineering Laboratory of Ecological Mariculture, Qingdao 266071, China.

出版信息

Sci Total Environ. 2023 May 1;871:162112. doi: 10.1016/j.scitotenv.2023.162112. Epub 2023 Feb 9.

Abstract

Climate change and intensifying human activity are posing serious threats to marine organisms. The fluctuating intertidal zone forms a miniature ecosystem of a rapidly changing environment for studying biological adaptation. Transgenerational plasticity (TGP), an evolutionary phenomenon in which parental experience influences offspring phenotypes, provides an avenue for adaptation, but the molecular mechanism was poorly understood in marine molluscs. In this study, wild Pacific oysters (Crassostrea gigas), which were collected from intertidal zones, were used to conduct two-generation breeding in a subtidal area combined with a heat shock experiment in the laboratory to investigate the intertidal environment-induced TGP under temperate subtidal condition and thermally exposed condition, respectively. We showed that TGP could influence the physiological phenotypes related to the status of oxidation and energy in non-stress-exposed subtidal offspring for at least two generations. Genomic DNA methylation exhibited heritable divergence between intertidal and subtidal oysters, and 1655 (or 42.83 %) differentially methylated genes (DMGs) in F were continuously reserved to F, which may mediate physiological TGP by participating in biological processes including macromolecule metabolism, cellular responses to stress, and the positive regulation of molecular function, especially fatty acid metabolism. The intertidal experience also influenced the thermal plasticity of physiological phenotypes within and across generations. Totally, 320 (or 14.74 %) specific thermal response DMGs in the intertidal F generation were identified in F and F, participating in pathways including carbohydrate, lipid, and energy metabolism, signal transduction, and the organismal immune system, which suggested transgenerational intertidal effect mediated by these genes could positively contribute to stress adaptation and had potential applications for aquaculture. This study demonstrates an epigenetic mechanism for TGP in stress adaptation in marine molluscs, and provides new avenues to improve the stress adaptation for marine resource conservation and aquaculture.

摘要

气候变化和人类活动的加剧对海洋生物构成了严重威胁。波动的潮间带形成了一个快速变化环境的微型生态系统,是研究生物适应的理想场所。跨代可塑性(TGP)是一种进化现象,即亲代的经验会影响后代的表型,为适应提供了途径,但在海洋软体动物中,其分子机制还知之甚少。在这项研究中,从潮间带收集的野生太平洋牡蛎(Crassostrea gigas)在亚潮带进行了两代繁殖,并结合实验室的热激实验,分别研究了温带亚潮带条件和热暴露条件下的潮间带环境诱导的 TGP。结果表明,TGP 至少可以影响非胁迫亚潮带后代与氧化和能量状态相关的生理表型达两代。基因组 DNA 甲基化表现出潮间带和亚潮带牡蛎之间的可遗传差异,并且 F 代中 1655 个(或 42.83%)差异甲基化基因(DMGs)连续保留到 F2 代,这可能通过参与生物过程(包括大分子代谢、细胞应激反应和分子功能的正向调节)来介导生理 TGP,特别是脂肪酸代谢。潮间带经历也会影响生理表型在代内和代间的热可塑性。总共在 F1 代的潮间带中鉴定到 320 个(或 14.74%)特定的热响应 DMGs,它们参与了包括碳水化合物、脂质和能量代谢、信号转导和机体免疫系统在内的途径,这表明这些基因介导的跨代潮间带效应可以积极促进应激适应,并具有水产养殖应用的潜力。该研究为海洋软体动物在应激适应中的 TGP 提供了一个表观遗传机制,并为海洋资源保护和水产养殖的应激适应提供了新的途径。

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