RNA-protein interactions in vivo: global gets specific

被引:70
作者
Aenkoe, Minna-Liisa [1 ]
Neugebauer, Karla M. [1 ]
机构
[1] Max Planck Inst Cell Biol & Genet, Dresden, Germany
关键词
TRACT-BINDING-PROTEIN; GENOME-WIDE ANALYSIS; GENERAL SPLICING REPRESSOR; MESSENGER-RNAS; STRUCTURAL BASIS; ANALYSIS REVEALS; VITRO SELECTION; MOLECULAR-BASIS; SR PROTEINS; RECOGNITION;
D O I
10.1016/j.tibs.2012.02.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
RNA-binding proteins (RBPs) impact every process in the cell; they act as splicing and polyadenylation factors, transport and localization factors, stabilizers and destabilizers, modifiers, and chaperones. RNA-binding capacity can be attributed to numerous protein domains that bind a limited repertoire of short RNA sequences. How is specificity achieved in cells? Here we focus on recent advances in determining the RNA-binding properties of proteins in vivo and compare these 10 in vitro determinations, highlighting insights into how endogenous RNA molecules are recognized and regulated. We also discuss the crucial contribution of structural determinations for understanding RNA-binding specificity and mechanisms.
引用
收藏
页码:255 / 262
页数:8
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