Serine/arginine-rich protein-dependent suppression of exon skipping by exonic splicing enhancers

被引:99
作者
Ibrahim, EC
Schaal, TD
Hertel, KJ
Reed, R
Maniatis, T
机构
[1] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
[2] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
[3] Univ Calif Irvine, Dept Microbiol & Mol Genet, Irvine, CA 92697 USA
关键词
intronic splicing silencers; pre-mRNA splicing; accurate splice-site recognition and pairing;
D O I
10.1073/pnas.0500543102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The 5' and 3' splice sites within an intron can, in principle, be joined to those within any other intron during pre-mRNA splicing. However, exons are joined in a strict 5' to 3' linear order in constitutively spliced pre-mRNAs. Thus, specific mechanisms must exist to prevent the random joining of exons. Here we report that insertion of exon sequences into an intron can inhibit splicing to the downstream 3' splice site and that this inhibition is independent of intron size. The exon sequences required for splicing inhibition were found to be exonic enhancer elements, and their inhibitory activity requires the binding of serine/arginine-rich splicing factors. We conclude that exonic enhancers can act as barriers to prevent exon skipping and thereby may play a key role in ensuring the correct 5' to 3' linear order of exons in spliced mRNA.
引用
收藏
页码:5002 / 5007
页数:6
相关论文
共 38 条
[1]   EXON RECOGNITION IN VERTEBRATE SPLICING [J].
BERGET, SM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (06) :2411-2414
[2]  
Black D L, 2003, Prog Mol Subcell Biol, V31, P187
[3]   Mechanisms of alternative pre-messenger RNA splicing [J].
Black, DL .
ANNUAL REVIEW OF BIOCHEMISTRY, 2003, 72 :291-336
[4]   Exonic splicing enhancers: mechanism of action, diversity and role in human genetic diseases [J].
Blencowe, BJ .
TRENDS IN BIOCHEMICAL SCIENCES, 2000, 25 (03) :106-110
[5]   Ser/Arg-rich protein-mediated communication between U1 and U2 small nuclear ribonucleoprotein particles [J].
Boukis, LA ;
Liu, N ;
Furuyama, S ;
Bruzik, JP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (28) :29647-29653
[6]   Listening to silence and understanding nonsense: Exonic mutations that affect splicing [J].
Cartegni, L ;
Chew, SL ;
Krainer, AR .
NATURE REVIEWS GENETICS, 2002, 3 (04) :285-298
[7]   The splicing factors 9G8 and SRp20 transactivate splicing through different and specific enhancers [J].
Cavaloc, Y ;
Bourgeois, CF ;
Kister, L ;
Stévenin, J .
RNA, 1999, 5 (03) :468-483
[8]   Human splicing factor ASF/SF2 encodes for a repressor domain required for its inhibitory activity on pre-mRNA splicing [J].
Dauksaite, V ;
Akusjärvi, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (15) :12579-12586
[9]   hnRNP A1 and the SR proteins ASF/SF2 and SC35 have antagonistic functions in splicing of β-tropomyosin exon 6B [J].
Expert-Bezançon, A ;
Sureau, A ;
Durosay, P ;
Salesse, R ;
Groeneveld, H ;
Lecaer, JP ;
Marie, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (37) :38249-38259