Splicing regulation: From a parts list of regulatory elements to an integrated splicing code

被引:720
作者
Wang, Zefeng [1 ]
Burge, Christopher B. [2 ]
机构
[1] Univ N Carolina, Sch Med, Dept Pharmacol, Chapel Hill, NC 27599 USA
[2] MIT, Dept Biol, Cambridge, MA 02139 USA
关键词
context dependence; pre-mRNA splicing; splicing code; splicing factor; splicing regulation;
D O I
10.1261/rna.876308
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alternative splicing of pre-mRNAs is a major contributor to both proteomic diversity and control of gene expression levels. Splicing is tightly regulated in different tissues and developmental stages, and its disruption can lead to a wide range of human diseases. An important long-term goal in the splicing field is to determine a set of rules or "code'' for splicing that will enable prediction of the splicing pattern of any primary transcript from its sequence. Outside of the core splice site motifs, the bulk of the information required for splicing is thought to be contained in exonic and intronic cis-regulatory elements that function by recruitment of sequence-specific RNA-binding protein factors that either activate or repress the use of adjacent splice sites. Here, we summarize the current state of knowledge of splicing cis-regulatory elements and their context-dependent effects on splicing, emphasizing recent global/genome-wide studies and open questions.
引用
收藏
页码:802 / 813
页数:12
相关论文
共 147 条
[101]   MAZ elements alter transcription elongation and silencing of the fibroblast growth factor receptor 2 exon IIIb [J].
Robson-Dixon, ND ;
Garcia-Blanco, MA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (28) :29075-29084
[102]   A conserved signal-responsive sequence mediates activation-induced alternative splicing of CD45 [J].
Rothrock, C ;
Cannon, B ;
Hahm, B ;
Lynch, KW .
MOLECULAR CELL, 2003, 12 (05) :1317-1324
[103]   HnRNP L represses exon splicing via a regulated exonic splicing silencer [J].
Rothrock, CR ;
House, AE ;
Lynch, KW .
EMBO JOURNAL, 2005, 24 (15) :2792-2802
[104]   Sequence features responsible for intron retention in human [J].
Sakabe, Noboru Jo ;
de Souza, Sandro Jose .
BMC GENOMICS, 2007, 8 (1)
[105]  
Schaal TD, 1999, MOL CELL BIOL, V19, P261
[106]   Members of the heterogeneous nuclear ribonucleoprotein H family activate splicing of an HIV-1 splicing substrate by promoting formation of ATP-dependent spliceosomal complexes [J].
Schaub, Michael C. ;
Lopez, Suzette R. ;
Caputi, Massimo .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (18) :13617-13626
[107]   Polypyrimidine tract binding protein blocks the 5′ splice site-dependent assembly of U2AF and the presplicelosomal E complex [J].
Sharma, S ;
Falick, AM ;
Black, DL .
MOLECULAR CELL, 2005, 19 (04) :485-496
[108]   Deletion of the N-terminus of SF2/ASF Permits RS-Domain-Independent Pre-mRNA Splicing [J].
Shaw, Stephanie D. ;
Chakrabarti, Sutapa ;
Ghosh, Gourisankar ;
Krainer, Adrian R. .
PLOS ONE, 2007, 2 (09)
[109]   RS domains contact splicing signals and promote splicing by a common mechanism in yeast through humans [J].
Shen, Haihong ;
Green, Michael R. .
GENES & DEVELOPMENT, 2006, 20 (13) :1755-1765
[110]   Arginine-serine-rich domains bound at splicing enhancers contact the branchpoint to promote prespliceosome assembly [J].
Shen, HH ;
Kan, JLC ;
Green, MR .
MOLECULAR CELL, 2004, 13 (03) :367-376