Genome-Wide Analysis of RNA Secondary Structure

被引:164
|
作者
Bevilacqua, Philip C. [1 ,2 ,3 ]
Ritchey, Laura E. [1 ,3 ]
Su, Zhao [4 ]
Assmann, Sarah M. [4 ]
机构
[1] Penn State Univ, Dept Chem, University Pk, PA 16802 USA
[2] Penn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USA
[3] Penn State Univ, Ctr RNA Mol Biol, University Pk, PA 16802 USA
[4] Penn State Univ, Dept Biol, University Pk, PA 16802 USA
来源
基金
美国国家科学基金会;
关键词
DMS-seq; genome-wide; in vivo RNA folding; RNA structurome; SHAPE; Structure-seq; NEAREST-NEIGHBOR PARAMETERS; LIVING CELLS; THERMODYNAMIC PARAMETERS; TRANSLATION INITIATION; STRUCTURE PREDICTION; PROTEIN INTERACTION; GENE-EXPRESSION; GLOBAL ANALYSIS; BASE-PAIRS; MOD-SEQ;
D O I
10.1146/annurev-genet-120215-035034
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Single-stranded RNA molecules fold into extraordinarily complicated secondary and tertiary structures as a result of intramolecular base pairing. In vivo, these RNA structures are not static. Instead, they are remodeled in response to changes in the prevailing physicochemical environment of the cell and as a result of intermolecular base pairing and interactions with RNA binding proteins. Remarkable technical advances now allow us to probe RNA secondary structure at single-nucleotide resolution and genome-wide, both in vitro and in vivo. These data sets provide new glimpses into the RNA universe. Analyses of RNA structuromes in HIV, yeast, Arabidopsis, and mammalian cells and tissues have revealed regulatory effects of RNA structure on messenger RNA (mRNA) polyadenylation, splicing, translation, and turnover. Application of new methods for genome-wide identification of mRNA modifications, particularly methylation and pseudouridylation, has shown that the RNA "epitranscriptome" both influences and is influenced by RNA structure. In this review, we describe newly developed genome-wide RNA structure-probing methods and synthesize the information emerging from their application.
引用
收藏
页码:235 / 266
页数:32
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