The roles of structural dynamics in the cellular functions of RNAs

被引:306
作者
Ganser, Laura R. [1 ]
Kelly, Megan L. [1 ]
Herschlag, Daniel [2 ,3 ,4 ]
Al-Hashimi, Hashim M. [1 ,5 ]
机构
[1] Duke Univ, Sch Med, Dept Biochem, Durham, NC 27708 USA
[2] Stanford Univ, Dept Biochem, Stanford ChEM H Chem Engn & Med Human Hlth, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Chem Engn, Stanford ChEM H Chem Engn & Med Human Hlth, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Chem, Stanford ChEM H Chem Engn & Med Human Hlth, Stanford, CA 94305 USA
[5] Duke Univ, Dept Chem, Durham, NC 27706 USA
基金
美国国家卫生研究院;
关键词
SECONDARY STRUCTURE; SMALL MOLECULES; CONFORMATIONAL ENSEMBLES; TERTIARY STRUCTURE; STRUCTURE REVEALS; PHASE-SEPARATION; GENE-EXPRESSION; PROTEIN-BINDING; INDUCED FIT; MECHANISM;
D O I
10.1038/s41580-019-0136-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
RNAs fold into 3D structures that range from simple helical elements to complex tertiary structures and quaternary ribonucleoprotein assemblies. The functions of many regulatory RNAs depend on how their 3D structure changes in response to a diverse array of cellular conditions. In this Review, we examine how the structural characterization of RNA as dynamic ensembles of conformations, which form with different probabilities and at different timescales, is improving our understanding of RNA function in cells. We discuss the mechanisms of gene regulation by microRNAs, riboswitches, ribozymes, post-transcriptional RNA modifications and RNA-binding proteins, and how the cellular environment and processes such as liquid-liquid phase separation may affect RNA folding and activity. The emerging RNA-ensemble-function paradigm is changing our perspective and understanding of RNA regulation, from in vitro to in vivo and from descriptive to predictive.
引用
收藏
页码:474 / 489
页数:16
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