Su Shengyan, Munganga Brian Pelekelo, Tian Can, Li Jianlin, Yu Fan, Li Hongxia, Wang Meiyao, He Xinjin, Tang Yongkai
Key Laboratory of Genetic Breeding and Aquaculture Biology of Freshwater Fishes, Ministry of Agriculture, Freshwater Fisheries Research Center, Chinese Academy of Fishery Sciences, Wuxi 214081, China.
Wuxi Fisheries College, Nanjing Agricultural University, Wuxi 214081, China.
Life (Basel). 2021 May 25;11(6):480. doi: 10.3390/life11060480.
In the present study, we used RNA-Seq to investigate the expression changes in the transcriptomes of two molting stages (postmolt (M) and intermolt (NM)) of the red swamp crayfish and identified differentially expressed genes. The transcriptomes of the two molting stages were de novo assembled into 139,100 unigenes with a mean length of 675.59 bp. The results were searched against the NCBI, NR, KEGG, Swissprot, and KOG databases, to annotate gene descriptions, associate them with gene ontology terms, and assign them to pathways. Furthermore, using the DESeq R package, differentially expressed genes were evaluated. The analysis revealed that 2347 genes were significantly ( > 0.05) differentially expressed in the two molting stages. Several genes and other factors involved in several molecular events critical for the molting process, such as energy requirements, hormonal regulation, immune response, and exoskeleton formation were identified and evaluated by correlation and KEGG analysis. The expression profiles of transcripts detected via RNA-Seq were validated by real-time PCR assay of eight genes. The information presented here provides a transient view of the hepatopancreas transcripts available in the postmolt and intermolt stage of crayfish, hormonal regulation, immune response, and skeletal-related activities during the postmolt stage and the intermolt stage.
在本研究中,我们使用RNA测序技术来研究红螯螯虾两个蜕皮阶段(蜕壳后阶段(M)和蜕壳间期(NM))转录组中的表达变化,并鉴定差异表达基因。将两个蜕皮阶段的转录组进行从头组装,得到139,100个单基因,平均长度为675.59 bp。将结果与NCBI、NR、KEGG、Swissprot和KOG数据库进行比对,以注释基因描述、将它们与基因本体学术语相关联并将它们分配到代谢途径中。此外,使用DESeq R包评估差异表达基因。分析显示,在两个蜕皮阶段有2347个基因存在显著(> 0.05)差异表达。通过相关性分析和KEGG分析,鉴定并评估了几个参与蜕皮过程关键分子事件的基因和其他因素,如能量需求、激素调节、免疫反应和外骨骼形成。通过对八个基因进行实时PCR检测,验证了通过RNA测序检测到的转录本的表达谱。本文提供的信息展示了小龙虾蜕壳后阶段和蜕壳间期肝胰腺转录本的概况,以及蜕壳后阶段和蜕壳间期的激素调节、免疫反应和骨骼相关活动。