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
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