生物
阿尔戈瑙特
基因沉默
小RNA
基因
RNA干扰
小核仁RNA
遗传学
基因敲除
掷骰子
细胞生物学
效应器
核酸外切酶
德罗沙
分子生物学
核糖核酸
非编码RNA
聚合酶
作者
GeunYoung Sim,Audrey C. Kehling,Mi Seul Park,Jackson Secor,Cameron Divoky,Huaqun Zhang,Nipun Malhotra,Divyaa Bhagdikar,Ekram W. Abd El–Wahab,Kotaro Nakanishi
标识
DOI:10.1073/pnas.2214335119
摘要
MicroRNAs (miRNAs) are about 22-nucleotide (nt) noncoding RNAs forming the effector complexes with Argonaute (AGO) proteins to repress gene expression. Although tiny RNAs (tyRNAs) shorter than 19 nt have been found to bind to plant and vertebrate AGOs, their biogenesis remains a long-standing question. Here, our in vivo and in vitro studies show several 3′→5′ exonucleases, such as interferon-stimulated gene 20 kDa (ISG20), three prime repair exonuclease 1 (TREX1), and ERI1 (enhanced RNAi, also known as 3′hExo), capable of trimming AGO-associated full-length miRNAs to 14-nt or shorter tyRNAs. Their guide trimming occurs in a manganese-dependent manner but independently of the guide sequence and the loaded four human AGO paralogs. We also show that ISG20-mediated guide trimming makes Argonaute3 (AGO3) a slicer. Given the high Mn 2+ concentrations in stressed cells, virus-infected cells, and neurodegeneration, our study sheds light on the roles of the Mn 2+ -dependent exonucleases in remodeling gene silencing.
科研通智能强力驱动
Strongly Powered by AbleSci AI