Fisheries College of Jimei University, Xiamen 361021, China; Key Laboratory of Healthy Mariculture for the East China Sea, Ministry of Agriculture and Rural Affairs, China.
Fisheries College of Jimei University, Xiamen 361021, China; Key Laboratory of Healthy Mariculture for the East China Sea, Ministry of Agriculture and Rural Affairs, China.
Gene. 2021 Jun 30;787:145642. doi: 10.1016/j.gene.2021.145642. Epub 2021 Apr 20.
Penaeus vannamei is the principle cultured shrimp species in China. However, with the increase of culture density, the growth difference between individuals is also expanding. Here, we make use of RNA-seq to study the growth mechanisms of P. vannamei. After 120 days, we examined the transcriptomes of rapid-growing individuals (RG) and slow-growing individuals (SG). A total of 2116 and 176 differentially expressed genes (DEGs) were found in SG and RG, respectively. Moreover, the main DEGs are opsin, heat shock protein (HSP), actin, myosin, superoxide dismutase (SOD), cuticle protein, and chitinase. GO analysis further revealed that the DEGs were enriched in biological processes significantly, such as "sensory perception," "sensory perception of light stimulus," "response to stimulus," and "response to stress." Additionally, KEGG enrichment analysis showed that the DEGs were mainly enriched in "pentose and glucuronate interconversions," "amino sugar and nucleotide sugar metabolism," "glycophospholipid biosynthesis," and "glutathione metabolism." Interestingly, the upstream genes in the ecdysone signaling pathway, including molting inhibition hormone (MIH) and crustacean hyperglycemic hormone (CHH), did not differ significantly between RG and SG, which suggests that the cause for the inconsistent growth performance is due to the stress levels rather than the ecdysone signal pathway. In summary, this work provides data that will be useful for future studies on shrimp growth and development.
凡纳滨对虾是中国主要的养殖虾种。然而,随着养殖密度的增加,个体之间的生长差异也在扩大。在这里,我们利用 RNA-seq 来研究凡纳滨对虾的生长机制。120 天后,我们检测了快速生长个体(RG)和缓慢生长个体(SG)的转录组。在 SG 和 RG 中分别发现了 2116 个和 176 个差异表达基因(DEGs)。此外,主要的 DEGs 是视蛋白、热休克蛋白(HSP)、肌动蛋白、肌球蛋白、超氧化物歧化酶(SOD)、甲壳质蛋白和几丁质酶。GO 分析进一步表明,DEGs 显著富集于生物学过程,如“感官感知”、“光刺激感官感知”、“对刺激的反应”和“对压力的反应”。此外,KEGG 富集分析表明,DEGs 主要富集于“戊糖和葡萄糖醛酸相互转化”、“氨基糖和核苷酸糖代谢”、“糖脂生物合成”和“谷胱甘肽代谢”。有趣的是,蜕皮激素信号通路中的上游基因,包括蜕皮抑制激素(MIH)和甲壳动物高血糖激素(CHH),在 RG 和 SG 之间没有显著差异,这表明生长表现不一致的原因是由于应激水平而不是蜕皮激素信号通路。总之,这项工作为未来的虾类生长和发育研究提供了有用的数据。