长期低盐和高盐胁迫下大琥珀幼体的脑转录组谱

IF 1.9 4区 农林科学 Q2 FISHERIES Aquaculture Research Pub Date : 2025-01-09 DOI:10.1155/are/2157396
Xiaoying Ru, Yang Huang, Tong Zhou, Tonglin Yang, Peipei Chen, Jiahui Yang, Chunhua Zhu, Hongjuan Shi
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引用次数: 0

摘要

鱼的大脑在调节生长、繁殖、发育和适应环境压力方面起着至关重要的作用。然而,很少有研究考察了整个鱼脑转录组及其对长期低盐和高盐胁迫的反应。大琥珀(Seriola dumerili)由于其高生长速度和优异的肉质,在全世界的海水养殖中具有很高的商业价值。因此,高通量RNA-Seq通过鉴定暴露于升高和/或降低盐度环境下的大琥珀大脑中的基因表达变化来阐明盐度适应的分子调控机制。我们将个体置于20、30和40 ppt(千分之一)的盐度水平下30天。在B30与B20组中共鉴定出272个(上调198个,下调74个)差异表达基因,在B30与B40组中鉴定出21个(上调10个,下调11个)差异表达基因,在B20与B40组中鉴定出343个(上调119个,下调224个)差异表达基因。转录组学分析显示,盐度胁迫影响了氨基酸代谢和转运相关基因(gpt、arg2、LOC111237759、slc3a2和slc7a5)、碳水化合物代谢(aldob、ldhba和gapdh)和信号转导(map3k8、map3k2、map2k7和lepr)的表达。京都基因与基因组百科全书(KEGG)富集分析表明,这些基因在代谢途径中显著富集,特别是在氨基酸和碳水化合物代谢、转录、翻译等方面。此外,基因集富集分析(GSEA)表明,代谢、信号转导、翻译、免疫系统以及运输和分解代谢途径在大脑中更为活跃。这些发现为进一步阐明海洋鱼类大脑盐度适应和转录调控的分子机制奠定了基础。
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Brain Transcriptome Profiles of Greater Amberjack (Seriola dumerili) Juveniles Under Long-Term Hypo- and Hypersaline Stress

The fish brain plays a crucial role in regulating growth, reproduction, development, and adaptation to environmental stress. However, there are few studies that have examined the entire fish brain transcriptome and its responses to long-term hypo- and hyper-salinity stress. Greater amberjack (Seriola dumerili) has a high commercial value in mariculture worldwide due to its high growth rate and excellent flesh quality. Consequently, high-throughput RNA-Seq was employed to elucidate the molecular regulatory mechanisms underlying salinity adaptation by identifying gene expression changes in the brain of greater amberjack exposed to elevated and/or reduced salinity environments. We subjected individuals to salinity levels of 20, 30, and 40 ppt (parts per thousand) for 30 days. A total of 272 (198 up-regulated and 74 down-regulated) differentially expressed genes (DEGs) were identified in the B30 vs. B20 group, 21 (10 up-regulated and 11 down-regulated) DEGs in the B30 vs. B40 group, and 343 (119 up-regulated and 224 down-regulated) DEGs in the B20 vs. B40 group. Transcriptomic analysis revealed that salinity stress influenced the expression of genes associated with amino acid metabolism and transport (gpt, arg2, LOC111237759, slc3a2, and slc7a5), carbohydrate metabolism (aldob, ldhba, and gapdh), and signal transduction (map3k8, map3k2, map2k7, and lepr). Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis indicated that the DEGs were significantly enriched in metabolism pathways, especially in amino acid and carbohydrate metabolism, transcription, translation, et cetera. Furthermore, gene set enrichment analysis (GSEA) demonstrated that the metabolism, signal transduction, translation, immune system, and transport and catabolism pathways were more active in the brain. These findings provide a foundation for further studies to clarify the molecular mechanisms of salinity adaptation and transcriptional regulation in the brain of marine fish.

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来源期刊
Aquaculture Research
Aquaculture Research 农林科学-渔业
CiteScore
4.60
自引率
5.00%
发文量
464
审稿时长
5.3 months
期刊介绍: International in perspective, Aquaculture Research is published 12 times a year and specifically addresses research and reference needs of all working and studying within the many varied areas of aquaculture. The Journal regularly publishes papers on applied or scientific research relevant to freshwater, brackish, and marine aquaculture. It covers all aquatic organisms, floristic and faunistic, related directly or indirectly to human consumption. The journal also includes review articles, short communications and technical papers. Young scientists are particularly encouraged to submit short communications based on their own research.
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