Exonic splicing enhancers: mechanism of action, diversity and role in human genetic diseases

被引:534
作者
Blencowe, BJ [1 ]
机构
[1] Univ Toronto, Charles H Best Inst, Dept Med Res, Toronto, ON M5G 1L6, Canada
关键词
D O I
10.1016/S0968-0004(00)01549-8
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
Exonic splicing enhancers (ESEs) are discrete sequences within exons that promote both constitutive and regulated splicing, The precise mechanism by which ESEs facilitate the assembly of splicing complexes has been controversial. However, recent studies have provided insights into this question and have led to a new model for ESE function, Other recent work has suggested that ESEs are comprised of diverse sequences and occur frequently within exons, Ominously, these latter studies predict that many human genetic diseases linked to mutations within exons might be caused by the inactivation of ESEs.
引用
收藏
页码:106 / 110
页数:5
相关论文
共 36 条
[1]   Cross-intron bridging interactions in the yeast commitment complex are conserved in mammals [J].
Abovich, N ;
Rosbash, M .
CELL, 1997, 89 (03) :403-412
[2]   EXON RECOGNITION IN VERTEBRATE SPLICING [J].
BERGET, SM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (06) :2411-2414
[3]   SR-related proteins and the processing of messenger RNA precursors [J].
Blencowe, BJ ;
Bowman, JAL ;
McCracken, S ;
Rosonina, E .
BIOCHEMISTRY AND CELL BIOLOGY, 1999, 77 (04) :277-291
[4]   The PWI motif: a new protein domain in splicing factors [J].
Blencowe, BJ ;
Ouzounis, CA .
TRENDS IN BIOCHEMICAL SCIENCES, 1999, 24 (05) :179-180
[5]   The SRm160/300 splicing coactivator subunits [J].
Blencowe, BJ ;
Baurén, G ;
Eldridge, AG ;
Issner, R ;
Nickerson, JA ;
Rosonina, E ;
Sharp, PA .
RNA, 2000, 6 (01) :111-120
[6]   A coactivator of pre-mRNA splicing [J].
Blencowe, BJ ;
Issner, R ;
Nickerson, JA ;
Sharp, PA .
GENES & DEVELOPMENT, 1998, 12 (07) :996-1009
[7]  
BURGE CB, 1999, RNA WORLD, V2
[8]   The regulation of splice-site selection, and its role in human disease [J].
Cooper, TA ;
Mattox, W .
AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (02) :259-266
[9]   Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements [J].
D'Souza, I ;
Poorkaj, P ;
Hong, M ;
Nochlin, D ;
Lee, VMY ;
Bird, TD ;
Schellenberg, GD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (10) :5598-5603
[10]   The SRm160/300 splicing coactivator is required for exon-enhancer function [J].
Eldridge, AG ;
Li, Y ;
Sharp, PA ;
Blencowe, BJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (11) :6125-6130