沈晔, 王兴强, 曹梅, 郑年昊, 陈百尧, 秦传新. 脊尾白虾对低盐胁迫响应的转录组学分析[J]. 南方水产科学, 2020, 16(5): 19-32. DOI: 10.12131/20190267
引用本文: 沈晔, 王兴强, 曹梅, 郑年昊, 陈百尧, 秦传新. 脊尾白虾对低盐胁迫响应的转录组学分析[J]. 南方水产科学, 2020, 16(5): 19-32. DOI: 10.12131/20190267
SHEN Ye, WANG Xingqiang, CAO Mei, ZHENG Nianhao, CHEN Baiyao, QIN Chuanxin. Transcriptome analysis of Exopalaemon carinicauda under low salinity stress[J]. South China Fisheries Science, 2020, 16(5): 19-32. DOI: 10.12131/20190267
Citation: SHEN Ye, WANG Xingqiang, CAO Mei, ZHENG Nianhao, CHEN Baiyao, QIN Chuanxin. Transcriptome analysis of Exopalaemon carinicauda under low salinity stress[J]. South China Fisheries Science, 2020, 16(5): 19-32. DOI: 10.12131/20190267

脊尾白虾对低盐胁迫响应的转录组学分析

Transcriptome analysis of Exopalaemon carinicauda under low salinity stress

  • 摘要: 转录组测序可在各种环境条件下对物种进行高通量测序,通过基因结构分析和功能注释,探讨特定条件下相关基因的功能和表达情况。该研究分别获取低盐胁迫组 (盐度0.2) 和自然海水组 (盐度31) 脊尾白虾 (Exopalaemon carinicauda) 样品,通过Illumina平台进行转录组测序,获得13.92 Gb高质量测序数据,组装得到111 618条转录本和72 734条Unigenes,其中有22 879条Unigenes得到注释,比对到Nr数据库的Unigenes为21 931条;筛选出1 492条脊尾白虾低盐胁迫差异显著表达基因,包括829条上调基因和663条下调基因,其中有810条差异表达基因得到注释。通过差异表达基因GO功能注释和富集分析及KEGG通路富集分析,锁定大量脊尾白虾在自然海水和淡水环境下的差异表达基因,为深入探讨脊尾白虾在低盐胁迫条件下的生理保护机制提供了技术支撑。

     

    Abstract: Transcriptome sequencing can be used for high-throughput sequencing of species under various environmental conditions. We explored the function and expression of related genes under specific conditions by gene structure analysis and gene function annotation. E. carinicauda samples at freshwater (salinity 0.2) and natural seawater (salinity 31) were sequenced by Illumina platform, and 13.92 Gb high-quality sequencing data was obtained. 111 618 transcripts and 72 734 unigenes were assembled. A total of 22 879 unigenes were annotated, of which 21 931 were compared to the Nr database. 1 492 differentially expressed genes were screened, including 829 up-regulated genes and 663 down-regulated genes, 810 of which were annotated. According to the GO function annotation, enrichment analysis and enrichment analysis of KEGG pathway of differentially expressed gene, we excavated differentially expressed genes of the natural seawater and freshwater environments, which provides technical support for further research on the physiological protection mechanism of E. carinicauda under low salinity stress.

     

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