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

miR-2188-5p promotes GCRV replication by the targeted degradation of klf2a in Ctenopharyngodon idellus

Yangyu Li, Liangming Chen, Yangyang Li, Ping Deng, Cheng Yang, Yongming Li, Lanjie Liao, Zuoyan Zhu, Yaping Wang, Rong Huang

Journal:DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY

IF:3.61

DOI:10.1016/j.dci.2022.104516

PMID:36084755

Published:2022-09-06

research field:分子生物学免疫学微生物学

Abstract

Studies on host immunity evasion by aquatic viruses have largely focused on coding genes. There is accumulating evidence for the important biological functions of non-coding miRNAs in virus–host interactions. The regulatory functions of non-coding miRNAs in fish reovirus–host interactions remain unknown. Here, miR-2188-5p in grass carp ( Ctenopharyngodon idellus ), a miRNA specific to teleosts, was predicted to target the 3′ UTR of the transcription factor klf2a . A correlation analysis and dual-luciferase reporter assay revealed that miR-2188-5p could induce the degradation of klf2a . The expression of miR-2188-5p induced the degradation of klf2a in a dose-dependent manner, suppressing the type I interferon response and promoting grass carp reovirus (GCRV) replication. As determined by a co-expression analysis , klf2a inhibited viral infection when miR-2188-5p was overexpressed. The targeted degradation of klf2a by miR-2188-5p could inhibit the type I interferon response and promote the replication of GCRV; however, this targeted degradation ability was insufficient to fully inhibit GCRV infection. These results provide novel insights into the regulatory effects and biological functions of non-coding miRNAs in fish–virus interactions.

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