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RNA-seq 联合蛋白质组学分析揭示了两种密切相关的海洋贻贝物种之间精子蛋白组的高度变异。

RNA-seq coupled to proteomic analysis reveals high sperm proteome variation between two closely related marine mussel species.

机构信息

Department of Biochemistry, Genetics and Immunology, Faculty of Biology, University of Vigo, Vigo, Spain; Marine Research Centre, University of Vigo (CIM-UVIGO), Isla de Toralla, Vigo, Spain.

Department of Biochemistry, Genetics and Immunology, Faculty of Biology, University of Vigo, Vigo, Spain.

出版信息

J Proteomics. 2019 Feb 10;192:169-187. doi: 10.1016/j.jprot.2018.08.020. Epub 2018 Sep 4.

Abstract

Speciation mechanisms in marine organisms have attracted great interest because of the apparent lack of substantial barriers to genetic exchange in marine ecosystems. Marine mussels of the Mytilus edulis species complex provide a good model to study mechanisms underlying species formation. They hybridise extensively at many localities and both pre- and postzygotic isolating mechanisms may be operating. Mussels have external fertilisation and sperm cells should show specific adaptations for survival and successful fertilisation. Sperm thus represent key targets in investigations of the molecular mechanisms underlying reproductive isolation. We undertook a deep transcriptome sequencing (RNA-seq) of mature male gonads and a 2DE/MS-based proteome analysis of sperm from Mytilus edulis and M. galloprovincialis raised in a common environment. We provide evidence of extensive expression differences between the two mussel species, and general agreement between the transcriptomic and proteomic results in the direction of expression differences between species. Differential expression is marked for mitochondrial genes and for those involved in spermatogenesis, sperm motility, sperm-egg interactions, the acrosome reaction, sperm capacitation, ATP reserves and ROS production. Proteins and their corresponding genes might thus be good targets in further genomic analysis of reproductive barriers between these closely related species. SIGNIFICANCE: Model systems for the study of fertilization include marine invertebrates with external fertilisation, such as abalones, sea urchins and mussels, because of the ease with which large quantities of gametes released into seawater can be collected after induced spawning. Unlike abalones and sea urchins, hybridisation has been reported between mussels of different Mytilus spp., which thus makes them very appealing for the study of reproductive isolation at both pre- and postzygotic levels. There is a lack of empirical proteomic studies on sperm samples comparing different Mytilus species, which could help to advance this study. A comparative analysis of sperm proteomes across different taxa may provide important insights into the fundamental molecular processes and mechanisms involved in reproductive isolation. It might also contribute to a better understanding of sperm function and of the adaptive evolution of sperm proteins in different taxa. There is now growing evidence from genomics studies that multiple protein complexes and many individual proteins might have important functions in sperm biology and the fertilisation process. From an applied perspective, the identification of sperm-specific proteins could also contribute to the improved understanding of fertility problems and as targets for fertility control.

摘要

海洋生物的物种形成机制引起了人们的极大兴趣,因为海洋生态系统中遗传交换的明显障碍很少。贻贝属的贻贝是研究物种形成机制的良好模型。它们在许多地方广泛杂交,并且可能存在前合子和后合子隔离机制。贻贝具有体外受精,精子细胞应该具有生存和成功受精的特定适应性。因此,精子是研究生殖隔离分子机制的关键目标。我们对在共同环境中饲养的贻贝属和马氏珠母贝的成熟雄性性腺进行了深度转录组测序(RNA-seq),并对精子进行了 2DE/MS 基于蛋白质组分析。我们提供了证据,证明这两种贻贝之间存在广泛的表达差异,并且转录组和蛋白质组结果在物种间表达差异的方向上具有很好的一致性。差异表达标记为线粒体基因和参与精子发生、精子运动、精子-卵子相互作用、顶体反应、精子获能、ATP 储备和 ROS 产生的基因。因此,蛋白质及其对应的基因可能是这些密切相关的物种之间生殖障碍的进一步基因组分析的良好目标。意义:受精的模式系统包括具有体外受精的海洋无脊椎动物,如鲍鱼、海胆和贻贝,因为在诱导产卵后很容易从海水中收集大量释放的配子。与鲍鱼和海胆不同,已报道不同贻贝属之间存在杂交,因此它们非常适合研究前合子和后合子水平的生殖隔离。关于比较不同贻贝物种的精子样本的蛋白质组学研究很少,这可能有助于推进这项研究。对不同分类群的精子蛋白质组进行比较分析可能为生殖隔离所涉及的基本分子过程和机制提供重要的见解。它还可能有助于更好地理解精子功能以及不同分类群中精子蛋白的适应性进化。越来越多的基因组学研究证据表明,多个蛋白质复合物和许多单个蛋白质可能在精子生物学和受精过程中具有重要功能。从应用的角度来看,鉴定精子特异性蛋白质也有助于更好地理解生育问题,并作为生育控制的靶标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0367/6309513/6e2c8f1d3331/nihms-1509222-f0002.jpg

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