Multi-disciplinary methods to define RNA-protein interactions and regulatory networks

被引:38
作者
Ascano, Manuel
Gerstberger, Stefanie
Tuschl, Thomas [1 ]
机构
[1] Rockefeller Univ, Howard Hughes Med Inst, New York, NY 10065 USA
关键词
GENOME-WIDE IDENTIFICATION; TRACT-BINDING-PROTEIN; POLYPYRIMIDINE TRACT; MESSENGER-RNAS; CROSS-LINKING; RECOGNITION; PURIFICATION; COMPLEXES; REVEALS; PUMILIO;
D O I
10.1016/j.gde.2013.01.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The advent of high-throughput technologies including deep-sequencing and protein mass spectrometry is facilitating the acquisition of large and precise data sets toward the definition of post-transcriptional regulatory networks. While early studies that investigated specific RNA-protein interactions in isolation laid the foundation for our understanding of the existence of molecular machines to assemble and process RNAs, there is a more recent appreciation of the importance of individual RNA-protein interactions that contribute to post-transcriptional gene regulation. The multitude of RNA-binding proteins (RBPs) and their many RNA targets has only been captured experimentally in recent times. In this review, we will examine current multidisciplinary approaches toward elucidating RNA-protein networks and their regulation.
引用
收藏
页码:20 / 28
页数:9
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