Context-dependent control of alternative splicing by RNA-binding proteins

被引:753
作者
Fu, Xiang-Dong [1 ,2 ]
Ares, Manuel, Jr. [3 ,4 ]
机构
[1] Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Inst Genom Med, La Jolla, CA 92093 USA
[3] Univ Calif Santa Cruz, Ctr Mol Biol RNA, Santa Cruz, CA 95064 USA
[4] Univ Calif Santa Cruz, Dept Mol Cell & Dev Biol, Santa Cruz, CA 95064 USA
基金
美国国家卫生研究院;
关键词
GENOME-WIDE ANALYSIS; CELL-FREE FORMATION; PRE-MESSENGER-RNAS; SR PROTEIN; HNRNP-L; EXON DEFINITION; COMBINATORIAL CONTROL; SECONDARY STRUCTURE; REGULATORY NETWORK; HITS-CLIP;
D O I
10.1038/nrg3778
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Sequence-specific RNA-binding proteins (RBPs) bind to pre-mRNA to control alternative splicing, but it is not yet possible to read the 'splicing code' that dictates splicing regulation on the basis of genome sequence. Each alternative splicing event is controlled by multiple RBPs, the combined action of which creates a distribution of alternatively spliced products in a given cell type. As each cell type expresses a distinct array of RBPs, the interpretation of regulatory information on a given RNA target is exceedingly dependent on the cell type. RBPs also control each other's functions at many levels, including by mutual modulation of their binding activities on specific regulatory RNA elements. In this Review, we describe some of the emerging rules that govern the highly context-dependent and combinatorial nature of alternative splicing regulation.
引用
收藏
页码:689 / 701
页数:13
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