Key Laboratory of Mariculture, Ocean University of China, Ministry of Education, Qingdao 266003, China.
Genes (Basel). 2020 Jun 8;11(6):631. doi: 10.3390/genes11060631.
is a euryhaline fish widely distributed in coastal, bay and estuarine areas, showing a strong tolerance to salinity. In order to understand the mechanism of adaptation to salinity stress, RNA-seq was used to compare the transcriptome responses of to the changes of salinity. Four salinity gradients, 0 psu, 15 psu (control), 30 psu and 45 psu were set to conduct the experiment. In total, 131,225 unigenes were obtained from the gill tissue of using the Illumina HiSeq 2000 platform (San Diego, USA). Compared with the gene expression profile of the control group, 572 differentially expressed genes (DEGs) were screened, with 150 at 0 psu, 170 at 30 psu, and 252 at 45 psu. Additionally, among these DEGs, Gene Ontology (GO) analysis indicated that binding, metabolic processes and cellular processes were significantly enriched. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways analysis detected 3, 5 and 8 pathways related to signal transduction, metabolism, digestive and endocrine systems at 0 psu, 30 psu and 45 psu, respectively. Based on GO enrichment analysis and manual literature searches, the results of the present study indicated that mainly responded to energy metabolism, ion transport and signal transduction to resist the damage caused by salinity stress. Eight DEGs were randomly selected for further validation by quantitative real-time PCR (qRT-PCR) and the results were consistent with the RNA-seq data.
是一种广布于沿海、海湾和河口区的广盐性鱼类,对盐度具有很强的耐受性。为了了解其适应盐度胁迫的机制,本研究采用 RNA-seq 技术比较了 对盐度变化的转录组响应。设置 0 psu、15 psu(对照)、30 psu 和 45 psu 四个盐度梯度进行实验。共从 鳃组织中获得了 131225 条 unigenes,使用 Illumina HiSeq 2000 平台(美国圣地亚哥)进行测序。与对照组的基因表达谱相比,筛选出 572 个差异表达基因(DEGs),其中 0 psu 时有 150 个,30 psu 时有 170 个,45 psu 时有 252 个。此外,这些 DEGs 中的基因本体论(GO)分析表明,结合、代谢过程和细胞过程显著富集。京都基因与基因组百科全书(KEGG)通路分析检测到 0 psu、30 psu 和 45 psu 分别与信号转导、代谢、消化和内分泌系统相关的 3、5 和 8 条通路。基于 GO 富集分析和文献检索,本研究结果表明, 主要通过能量代谢、离子转运和信号转导来应对盐度胁迫造成的损伤。随机选择了 8 个 DEGs 进行定量实时 PCR(qRT-PCR)验证,结果与 RNA-seq 数据一致。