分子生物学
IVD分子诊断
细胞培养与分析
蛋白研究
细胞因子
重组蛋白
抗体
高通量测序建库
病原检测UCF系列
生物医药
工具酶
抑制剂激活剂与常用试剂
仪器
耗材

Comparative analysis of testis transcriptome between a genetic male sterile line (GMS) and its wild-type 898WB in silkworm, Bombyx mori

Xinglin Mei, Mengjie Gao, Tianchen Huang, Dongxu Shen, Dingguo Xia, Zhiyong Qiu, Qiaoling Zhao

Journal:Comparative Biochemistry and Physiology D-Genomics & Proteomics

IF:3.31

DOI:10.1016/j.cbd.2022.100961

PMID:35074722

Published:2022-01-15

research field:肿瘤学肿瘤微环境分子生物学免疫学癌症免疫治疗

Abstract

The silkworm , Bombyx mori , is an important model organism of lepidopteran insects, and its testis is a main male reproductive organ and spermatogenesis place. Studying the testis helps to understand the mechanisms of genetic sterility of lepidopteran insects and to achieve sterile insect technique (SIT) for pest control. Herein, we performed a comparative transcriptome analysis of testes between three biological replicates of the GMS mutant and wild strain 898WB, respectively. In total, 1872 up-regulated genes and 1823 down-regulated genes were identified in the testis of the GMS mutant. Several genes contribute significantly to spermatogenesis and testis development , such as “serine/threonine protein kinase”, “organic cation transporter protein”, “tyrosine protein kinase”, “lncRNAs” and “immune-associated genes”. The KEGG pathway analysis shows that the DEGs were annotated to 123 pathways, and 10 pathways were significantly enriched, such as “metabolic pathway”, “biosynthesis of amino acids”, and “phagosome–lysosome pathway”, which are associated with testis development and spermatogenesis. The results of the qPCR expression were consistent with the RNA-seq data, which shows that the RNA-seq results were accurate. The DEGs of the testes between GMS mutant and 898WB were screened by RNA-Seq technology, which provides a reliable reference to understand the molecule mechanism of male sterility of the GMS mutant.

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