基于转录组学的鲈鱼生长迟缓分析

IF 2.2 2区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Comparative Biochemistry and Physiology D-Genomics & Proteomics Pub Date : 2024-07-23 DOI:10.1016/j.cbd.2024.101298
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引用次数: 0

摘要

大鳞鲈是世界许多地区具有重要经济价值的甲壳类动物,但近年来,生长迟缓已成为一个日益严重的问题。虽然根本原因尚不清楚,但这已不可避免地影响到水产养殖和产量。在这项研究中,利用高通量测序技术对具有明显生长差异的罗氏鲈的鳃、肝胰腺和肌肉组织样本进行了转录组测序和生物信息学分析。共注释了 59,796 个单基因。差异表达分析表明,在鳃组织中筛选出的差异表达基因(DEGs)最多(1790 个 DEGs)。在肌肉和肝胰腺组织中,分别筛选出了 696 个和 598 个 DEGs。这些 DEGs 被注释到《京都基因和基因组百科全书》的通路中,发现了几个与生长代谢相关的显著富集通路,如 PI3K-AKT、糖酵解/糖元生成、淀粉和蔗糖代谢。这些结果表明,生长代谢水平低可能是 M. rosenbergii 生长迟缓的原因之一。我们的数据为进一步研究 M. rosenbergii 生长迟缓的原因和分子机制提供了支持。
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Transcriptomics-based analysis of Macrobrachium rosenbergii growth retardation

Macrobrachium rosenbergii is an economically important crustacean in many parts of the world, but in recent years, growth retardation has become an increasingly serious issue. While the underlying causes remain unclear, this has inevitably impacted on aquaculture and production outputs. In this study, gill, hepatopancreas, and muscle tissue samples from M. rosenbergii, with distinct growth differences, underwent transcriptome sequencing and bioinformatics analyses using high-throughput sequencing. In total, 59,796 unigenes were annotated. Differential expression analyses showed that the most differentially expressed genes (DEGs) were screened in gill tissue (1790 DEGs). In muscle and hepatopancreas tissues, 696 and 598 DEGs were screened, respectively. These DEGs were annotated to Kyoto Encyclopedia of Genes and Genomes pathways, which identified several significantly enriched pathways related to growth metabolism, such as PI3K-AKT, glycolysis/gluconeogenesis, and starch and sucrose metabolism. These results suggest that low growth metabolism levels may be one cause of M. rosenbergii growth retardation. Our data provide support for further investigations into the causes and molecular mechanisms underpinning growth retardation in M. rosenbergii.

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来源期刊
CiteScore
5.10
自引率
3.30%
发文量
69
审稿时长
33 days
期刊介绍: Comparative Biochemistry & Physiology (CBP) publishes papers in comparative, environmental and evolutionary physiology. Part D: Genomics and Proteomics (CBPD), focuses on “omics” approaches to physiology, including comparative and functional genomics, metagenomics, transcriptomics, proteomics, metabolomics, and lipidomics. Most studies employ “omics” and/or system biology to test specific hypotheses about molecular and biochemical mechanisms underlying physiological responses to the environment. We encourage papers that address fundamental questions in comparative physiology and biochemistry rather than studies with a focus that is purely technical, methodological or descriptive in nature.
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