Research Center for Quality, Safety and Risk Assessment of Grass and Livestock Products, Institute of Grassland Research, Chinese Academy of Agricultural Sciences, Hohhot, China.
College of Horticulture and Plant Protection, Inner Mongolia Agricultural University, Hohhot, China.
Arch Insect Biochem Physiol. 2021 Jun;107(2):e21789. doi: 10.1002/arch.21789. Epub 2021 Apr 16.
Exorista civilis Rondani (Diptera:Tachinidae) is an excellent dominant parasitic enemy all over the world. But there has been a lack of research on the molecular regulation of diapause in E. civilis. To investigate the important diapause-associated genes and metabolic pathways in E. civilis, we can provide a theoretical basis for clarifying the molecular mechanism of diapause at the transcriptome level. The Illumina HiSeq. 2000 platform was used to perform transcriptome sequencing and bioinformatics analysis of the non-diapause and diapause pupae of E. civilis. 58,050 unigenes were successfully assembled, in which 4355 upregulated and 3158 downregulated unigenes were differentially expressed. Moreover, by Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichments, 896 kinds of the differentially expressed genes were specifically analyzed and showed that diapause-associated genes were related to be involved in the pathways of cold resistance, amino acid metabolism, and energy metabolism. Furthermore, these upregulated five genes showed the same trends of expression patterns between quantitative real-time polymerase chain reaction and RNA-Seq. This study provides a theoretical basis for the further study of the diapausing molecular mechanisms of E. civilis.
黄腹追寄蝇(Diptera:Tachinidae)是一种在全世界都具有卓越优势的寄生性天敌昆虫。但对于黄腹追寄蝇滞育的分子调控研究却相对较少。为了研究黄腹追寄蝇滞育相关的重要基因和代谢途径,我们可以在转录组水平上为阐明滞育的分子机制提供理论依据。本研究利用 Illumina HiSeq. 2000 平台对非滞育和滞育蛹期的黄腹追寄蝇进行了转录组测序和生物信息学分析。成功组装了 58050 条 unigenes,其中有 4355 个上调和 3158 个下调的 unigenes表现出差异表达。此外,通过京都基因与基因组百科全书(KEGG)通路富集分析,对 896 种差异表达基因进行了特异性分析,结果表明滞育相关基因与抗寒、氨基酸代谢和能量代谢途径有关。进一步研究发现,这 5 个上调基因的表达模式与实时荧光定量聚合酶链式反应(qPCR)和 RNA-Seq 的结果一致。本研究为进一步研究黄腹追寄蝇的滞育分子机制提供了理论基础。