Anatomy of four human Argonaute proteins

被引:56
|
作者
Nakanishi, Kotaro [1 ,2 ]
机构
[1] Ohio State Univ, Dept Chem & Biochem, Columbus, OH 43210 USA
[2] Ctr RNA Biol, Columbus, OH 43210 USA
关键词
CRYSTAL-STRUCTURE; STRUCTURAL BASIS; RNA RECOGNITION; INTELLECTUAL DISABILITY; TARGET RECOGNITION; GUIDE RNA; BINDING; PHOSPHORYLATION; RISC; DOMAIN;
D O I
10.1093/nar/gkac519
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs (miRNAs) bind to complementary target RNAs and regulate their gene expression post-transcriptionally. These non-coding regulatory RNAs become functional after loading into Argonaute (AGO) proteins to form the effector complexes. Humans have four AGO proteins, AGO1, AGO2, AGO3 and AGO4, which share a high sequence identity. Since most miRNAs are found across the four AGOs, it has been thought that they work redundantly, and AGO2 has been heavily studied as the exemplified human paralog. Nevertheless, an increasing number of studies have found that the other paralogs play unique roles in various biological processes and diseases. In the last decade, the structural study of the four AGOs has provided the field with solid structural bases. This review exploits the completed structural catalog to describe common features and differences in target specificity across the four AGOs.
引用
收藏
页码:6618 / 6638
页数:21
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