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长读测序揭示了对不同盐度条件的转录组响应。

Transcriptome Responses to Different Salinity Conditions in Revealed by Long-Read Sequencing.

机构信息

CAS and Shandong Province Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China.

Laboratory of Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266237, China.

出版信息

Genes (Basel). 2024 Feb 28;15(3):317. doi: 10.3390/genes15030317.

Abstract

The marine nematode is widely distributed in intertidal zones around the globe, yet the mechanisms underlying its broad adaptation to salinity remain elusive. In this study, we applied ONT long-read sequencing technology to unravel the transcriptome responses to different salinity conditions in . Through ONT sequencing under 3‱, 30‱ and 60‱ salinity environments, we obtained 131.78 G clean data and 26,647 non-redundant long-read transcripts, including 6464 novel transcripts. The DEGs obtained from the current ONT lrRNA-seq were highly correlated with those identified in our previously reported Illumina short-read RNA sequencing data. When we compared the 30‱ to the 3‱ salinity condition, we found that GO terms such as oxidoreductase activity, cation transmembrane transport and ion transmembrane transport were shared between the ONT lrRNA-seq and Illumina data. Similarly, GO terms including extracellular space, structural constituents of cuticle, substrate-specific channel activity, ion transport and substrate-specific transmembrane transporter activity were shared between the ONT and Illumina data under 60‱ compared to 30‱ salinity. In addition, we found that 79 genes significantly increased, while 119 genes significantly decreased, as the salinity increased. Furthermore, through the GO enrichment analysis of 214 genes containing DAS, in 30‱ compared to 3‱ salinity, we found that GO terms such as cellular component assembly and coenzyme biosynthetic process were enriched. Additionally, we observed that GO terms such as cellular component assembly and coenzyme biosynthetic process were also enriched in 60‱ compared to 30‱ salinity. Moreover, we found that 86, 125, and 81 genes that contained DAS were also DEGs, in comparisons between 30‱ and 3‱, 60‱ and 30‱, and 60‱ and 3‱ salinity, respectively. In addition, we demonstrated the landscape of alternative polyadenylation in marine nematode under different salinity conditions This report provides several novel insights for the further study of the mechanisms by which euryhalinity formed and evolved, and it might also contribute to the investigation of salinity dynamics induced by global climate change.

摘要

海洋线虫广泛分布于全球潮间带,但它们广泛适应盐度的机制仍不清楚。在这项研究中,我们应用ONT 长读测序技术来揭示在不同盐度条件下的转录组反应。通过在 3‰、30‰和 60‰盐度环境下进行 ONT 测序,我们获得了 131.78 G 的清洁数据和 26647 条非冗余的长读转录本,其中包括 6464 条新转录本。从当前的 ONT lrRNA-seq 中获得的 DEGs 与我们之前报道的 Illumina 短读 RNA 测序数据中鉴定的 DEGs 高度相关。当我们将 30‰与 3‰盐度条件进行比较时,我们发现 ONT lrRNA-seq 和 Illumina 数据之间共享氧化还原酶活性、阳离子跨膜运输和离子跨膜运输等 GO 术语。同样,在 60‰与 30‰盐度条件下,ONT 和 Illumina 数据之间共享包括细胞外空间、角质层结构成分、底物特异性通道活性、离子运输和底物特异性跨膜转运体活性等 GO 术语。此外,我们发现随着盐度的增加,79 个基因显著增加,而 119 个基因显著减少。此外,通过对包含 DAS 的 214 个基因进行 GO 富集分析,我们发现与 3‰相比,在 30‰盐度条件下,细胞成分组装和辅酶生物合成过程等 GO 术语得到了富集。此外,我们观察到在 60‰与 30‰盐度条件下,细胞成分组装和辅酶生物合成过程等 GO 术语也得到了富集。此外,我们发现 86、125 和 81 个包含 DAS 的基因在 30‰与 3‰、60‰与 30‰和 60‰与 3‰盐度条件下的比较中也是 DEGs。此外,我们还展示了海洋线虫在不同盐度条件下的可变多聚腺苷酸化景观。本报告为进一步研究广盐性形成和进化的机制提供了一些新的见解,也可能有助于研究全球气候变化引起的盐度动态。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e91a/10970011/a29acac41695/genes-15-00317-g001.jpg

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