昆虫学报 ›› 2023, Vol. 66 ›› Issue (9): 1221-1232.doi: 10.16380/j.kcxb.2023.09.009

• 研究论文 • 上一篇    下一篇

刺猎蝽属种间转录组比较分析

邓美菁1, 赵萍2,*   

  1. (1.南宁师范大学, 环境与生命科学学院, 南宁 530100; 2. 南宁师范大学, 地理与海洋研究院, 南宁 530100)
  • 出版日期:2023-09-20 发布日期:2023-09-27

Interspecific comparative analysis of transcriptome in the genus Sclomina

DENG Mei-Jing1, ZHAO Ping2,*   

  1.  (1. School of Environmental and Life Sciences, Nanning Normal University, Nanning 530100, China; 2. Institute of Geography and Oceanography, Nanning Normal University, Nanning 530100, China)
  • Online:2023-09-20 Published:2023-09-27

摘要: 【目的】建立刺猎蝽属Sclomina 3种的转录组数据库,分析近缘种间转录组表达差异,探讨在转录组水平的种间趋异情况。【方法】采用Illumina HiSeqTM4000高通量测序平台进行刺猎蝽属齿缘刺猎蝽S. erinacea、兴仁刺猎蝽S. xingrensis和广西刺猎蝽S. guangxiensis 3种转录组测序;利用Nr, Swiss-Prot, COG/KOG和KEGG 数据库进行基因功能注释;对种间差异表达基因(differentially expressed genes, DEGs)进行GO功能注释和KEGG通路富集分析。【结果】齿缘刺猎蝽、兴仁刺猎蝽和广西刺猎蝽转录组测序组装获得42 215个unigenes。21 117个基因在上述4个数据库中得到注释(各数据库注释基因数为: Nr, 20 522; Swiss-Prot, 15 550; COG/KOG, 13 969; KEGG,10 850)。兴仁刺猎蝽vs齿缘刺猎蝽转录组有3 390个DEGs (803个上调,2 587个下调),兴仁刺猎蝽vs广西刺猎蝽转录组有12 543个DEGs (6 639个上调,5 904个下调),齿缘刺猎蝽vs广西刺猎蝽转录组有3 580个DEGs(2 485个上调,1 095个下调)。GO功能注释结果显示,上述DEGs被注释到生物学过程、细胞组分和分子功能3个功能大类和功能亚类,兴仁刺猎蝽vs齿缘刺猎蝽转录组中DEGs分别注释到代谢过程、细胞和细胞部分等50个功能亚类中,下调基因多,上调基因少;兴仁刺猎蝽vs广西刺猎蝽转录组中DEGs被注释到生物学过程、细胞部分和细胞等54个功能亚类中;齿缘刺猎蝽vs广西刺猎蝽转录组中DEGs被分别注释到细胞部分、代谢过程等46个功能亚类中。6 254个DEGs被注释到KEGG代谢通路,涉及多个不同的代谢通路,包括代谢通路、药物代谢细胞色素P450、核糖体等;兴仁刺猎蝽vs齿缘刺猎蝽转录组702个DEGs富集到164个KEGG通路;兴仁刺猎蝽 vs广西刺猎蝽转录组中2 091个DEGs富集得到201个KEGG通路;齿缘刺猎蝽vs广西刺猎蝽转录组中865个DEGs富集得到129个KEGG通路;兴仁刺猎蝽vs广西刺猎蝽转录组DEGs富集到代谢通路、药物代谢细胞色素P450和核糖体等KEGG通路的数量最多。【结论】本研究结果丰富了刺猎蝽属的分子生物学数据;在转录组水平上呈现了齿缘刺猎蝽、兴仁刺猎蝽和广西刺猎蝽的种间差异,探索了该属物种分化的实际情况。

关键词: 刺猎蝽属, 高通量测序, 转录组, 差异表达基因

Abstract: 【Aim】To establish the transcriptome databases of three species of the genus Sclomina, analyze the expression differences of transcriptomes among related species, and investigate the interspecific divergence at the transcriptome level.【Methods】The Illumina HiSeqTM4000 high-throughput sequencing platform was used for transcriptome sequencing in the three Sclomina species, S. erinacea, S. xingrensis and S. guangxiensis. The gene function annotation was conducted by using Nr, Swiss-Prot, COG/KOG and KEGG databases. The GO functional annotation and KEGG pathway enrichment analysis were performed for the interspecific differentially expressed genes (DEGs).【Results】A total of 42 215 unigenes were obtained by transcriptome sequencing of S. erinacea, S. xingrensis and S. guangxiensis. A total of 21 117 genes were annotated in the above four databases (number of genes: Nr, 20 522; Swiss-Prot, 15 550; COG/KOG, 13 969, KEGG, 10 850). There were 3 390 DEGs (803 up-regulated, 2 587 down-regulated) in the S. xingrensis vs S. erinacea transcriptomes, 12 543 DEGs (6 639 up-regulated, 5 904 down-regulated) in the S. xingrensis vs S. guangxiensis transcriptomes, and 3 580 DEGs (2 485 up-regulated, 1 095 down-regulated) in the S. erinacea vs S. guangxiensis transcriptomes. GO functional annotation result showed that all of the above DEGs were annotated into three functional classes including biological process, cellular component and molecular function, and some functional subclasses. The DEGs in the S. xingrensis vs S. erinacea transcriptomes were annotated into 50 functional subclasses, such as metabolic process, cell and cell part, and more genes were down-regulated, and a few genes were up-regulated. The DEGs in the S. xingrensis vs S. guangxiensis transcriptomes were annotated into 54 functional subclasses, such as biological process, cell part and cell. The DEGs in the S. erinacea vs S. guangxiensis transcriptomes were annotated into 46 functional subclasses, such as cell part and metabolic process. A total of 6 254 DEGs were annotated to KEGG metabolic pathways involving several different metabolic pathways, including metabolic pathway, drug metabolism-cytochrome P450, ribosome, etc. A total of 702 DEGs in the S. xingrensis vs S. erinacea transcriptomes were enriched in 164 KEGG pathways. A total of 2 091 DEGs in the S. xingrensis vs S. guangxiensis transcriptomes were enriched to 201 KEGG pathways. A total of 865 DEGs in the S. erinacea vs S. guangxiensis transcriptomes were enriched to 129 KEGG pathways. The number of DEGs enriched in metabolic pathway, drug metabolism-cytochrome P450 and ribosome in the S. xingrensis vs S. guangxiensis transcriptomes was the highest.【Conclusion】This study results enrich the molecular biological data of the genus Sclomina. At the level of transcriptome, the interspecies difference in S. erinacea, S. xingrensis and S. guangxiensis, and the actual situation of species divergence in this genus Sclomina are explored.

Key words: Sclomina, high-throughput sequencing, transcriptome, differentially expressed genes