比较转录组初步揭示了克氏原螯虾生长速率的分子机制

Yude Wang , Dishan Hong , Jiajun Yao , Huifang Tan , Shi Wang , Jinlong Li , Yaxin Luo , Dongwu Wang , Shaojun Liu
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引用次数: 0

摘要

克氏原螯虾(Procambarus clarkii)是众所周知的入侵物种。它已成为中国最重要的淡水养殖资源之一。本研究报道了克氏原螯虾的核型和全线粒体基因组。此外,我们还对来自两个不同体型种群的克氏原螯虾进行了转录组分析。随机选取体型较大的3只,即LS组,体长16.24 ~ 18.85 cm,体重38.96 ~ 45.36 g。随机选取体长10.50 ~ 12.70 cm、体重19.56 ~ 25.95 g的3只小个体,即SS组。对克氏原螯虾进行转录组比较分析,共发现36个差异表达基因(DEGs),其中SS组有20个基因上调,16个基因下调。功能分析显示,4个基因(金属还原酶Steap4样(Steap4)、肌球蛋白重链快骨骼肌、肌样(MH)、卵磷脂膜外层蛋白i样(VMO-I)、酸性和富含半胱氨酸的分泌蛋白(SPARC))参与了克拉氏杆菌细胞增殖、肌肉生长和能量代谢的调控,提示4个基因与克拉氏杆菌的生长有关。我们利用实时荧光定量PCR验证了这四个差异表达基因在LS和SS中的表达水平。这些结果提供了对克氏杆菌生长差异的调控机制的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative transcriptome preliminary reveals the molecular mechanism of the growth rate of Procambarus clarkii

The red swamp crayfish (Procambarus clarkii) is a well-known invasive species. It has become one of the most important freshwater aquaculture resources in China. In this study, we reported the karyotype and whole mitochondrial genome of Procambarus clarkii. In addition, we performed transcriptome analysis of Procambarus clarkii from two different body size populations. The three large individuals, namely, the LS group, were randomly chosen, with body lengths and weights of 16.24–18.85 ​cm and 38.96–45.36 ​g, respectively. The three small individuals, namely, the SS group, were randomly chosen, with body lengths and weights of 10.50–12.70 ​cm and 19.56–25.95 ​g, respectively. Comparative transcriptomic analysis of Procambarus clarkii characterized 36 differentially expressed genes (DEGs), comprising 20 upregulated genes and 16 downregulated genes in the SS group. Functional analyses revealed that four genes (metalloreductase STEAP4-like (Steap4), myosin heavy chain fast skeletal muscle, muscle-like (MH), vitelline membrane outer layer protein I-like protein (VMO-I), and secreted protein acidic and rich in cysteine (SPARC)) were involved in the regulation of cell proliferation, muscle growth and energy metabolism, suggesting that four genes were related to growth in P. clarkii. We validated the expression levels of these four differentially expressed genes in LS and SS using Quantitative real-time PCR. These results provide insights into the regulatory mechanisms underlying the difference in P. clarkii growth.

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