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High throughput sequencing of RNA transcriptomes in Ruditapes philippinarum identifies genes involved in osmotic stress response

机译:菲律宾Ruditapes中RNA转录组的高通量测序可鉴定涉及渗透胁迫反应的基因

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摘要

Ruditapes philippinarum, is an economically important marine bivalve species. The ability to cope with low salinity stress is quite important for the survival of aquatic species under natural conditions. In this study, the transcriptional response of the Manila clam to low salinity stress was characterized using RNA sequencing. The transcriptomes of a low salinity-treatment group (FRp1, FRp2), which survived under low salinity stress, and control group (SRp1, SRp2), which was not subjected to low salinity stress, were sequenced with the Illumina HiSeq platform. A total of 196,578 unigenes were generated. GO and KEGG analyses revealed that signal transduction, immune response, cellular component organization or biogenesis, and energy production processes were the most highly enriched pathways among the genes that were differentially expressed under low salinity stress. All these pathways could be assigned to the following biological functions in the low salinity tolerant Manila clam: signal response to low salinity stress, antioxidant response, intracellular free amino acid transport and metabolism, energy production and conversion, cell signaling pathways, and regulation of ionic content and cell volume. In summary, this is the first study using high-throughput sequencing to identify gene targets that could explain osmotic regulation mechanisms under salinity stress in R. philippinarum.
机译:Ruditapes philippinarum,是一种经济上重要的海洋双壳类。应对低盐度胁迫的能力对于自然条件下水生物种的生存非常重要。在这项研究中,使用RNA测序表征了马尼拉蛤对低盐度胁迫的转录反应。用Illumina HiSeq平台对低盐度处理组(FRp1,FRp2)和低盐度处理组(SRp1,SRp2)的转录组进行测序。总共产生了196,578个单基因。 GO和KEGG分析表明,在低盐度胁迫下差异表达的基因中,信号转导,免疫应答,细胞成分的组织或生物发生以及能量产生过程是最丰富的途径。在耐盐度低的马尼拉蛤中,所有这些途径都可以分配给以下生物学功能:对低盐度胁迫的信号响应,抗氧化剂响应,细胞内游离氨基酸转运和代谢,能量产生和转化,细胞信号传导途径以及离子调节含量和细胞体积。总而言之,这是第一项使用高通量测序来鉴定可解释盐渍胁迫下盐胁迫下渗透调节机制的基因靶标的研究。

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