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首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >De novo assembly and transcriptome analysis of osmoregulation in Litopenaeus vannamei under three cultivated conditions with different salinities
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De novo assembly and transcriptome analysis of osmoregulation in Litopenaeus vannamei under three cultivated conditions with different salinities

机译:不同盐度三种耕作条件下南美白对虾渗透调节的从头组装和转录组分析

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Litopenaeus vannamei, one of the most important euryhaline crustaceans, is cultured in seawater, brackish water, and freshwater worldwide. We performed Illumina RNA sequencing of L. vannamei gills, generating 124,914,870; 119,250,450; and 105,487,350 raw reads from the shrimps cultured in seawater, brackish water, and freshwater, respectively. From these reads, 466,293 transcripts were de novo assembled and annotated. Comparative genomic analysis showed that 1752 genes were significantly differentially expressed in the freshwater group compared with the seawater group, including 1242 upregulated and 510 downregulated genes. In addition, 1246 genes were differentially expressed in the brackish group vs. the seawater water group, including 659 upregulated and 587 downregulated genes. These differentially expressed genes were mainly involved in energy metabolism, substance metabolism, ion transport and signal transduction, and genetic process. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway enrichment analysis were used to analyze the functional significance of the differentially expressed genes, included those responding to salinity through diverse biological functions and processes and numerous potential genes associated with the osmotic response. L vannamei responses to the three cultivated salinities were analyzed using next-generation sequencing. The transcriptional database established from the current research adds to the information available on L vannamei and the findings expand our knowledge of the molecular basis of osmoregulation mechanisms in this species. (C) 2015 Elsevier B.V. All rights reserved.
机译:凡纳滨对虾(Litopenaeus vannamei)是最重要的淡季甲壳类动物之一,在全世界的海水,微咸水和淡水中都有养殖。我们对南美白对虾进行Illumina RNA测序,产生124,914,870; 119,250,450;分别从海水,微咸水和淡水中养殖的虾中读取了105,487,350个原始读物。从这些读物中,重新组装并注释了466,293个转录物。比较基因组分析表明,与海水组相比,淡水组的1752个基因表达差异显着,其中包括1242个上调基因和510个下调基因。另外,在咸淡水组与海水组中有1246个基因差异表达,包括659个上调基因和587个下调基因。这些差异表达的基因主要参与能量代谢,物质代谢,离子转运和信号转导以及遗传过程。使用基因本体论和《京都议定书》全书中的基因和基因组途径富集分析来分析差异表达基因的功能意义,包括那些通过多种生物学功能和过程对盐分作出反应的基因以及与渗透反应相关的众多潜在基因。使用下一代测序分析了南美白对南美白对盐分的响应。从当前研究建立的转录数据库增加了南美白对虾的可用信息,这些发现扩展了我们对该物种渗透调节机制的分子基础的认识。 (C)2015 Elsevier B.V.保留所有权利。

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