A polar mechanism coordinates different regions of alternative splicing within a single gene

被引:53
作者
Fededa, JP
Petrillo, E
Gelfand, MS
Neverov, AD
Kadener, S
Nogués, G
Pelisch, F
Baralle, FE
Muro, AF
Kornblihtt, AR
机构
[1] Univ Buenos Aires, Lab Fisiol & Biol Mol, Dept Fisiol Biol Mol & Celular, IFIBYNE,CONICET,Fac Ciencias Exactas & Nat, Buenos Aires, DF, Argentina
[2] Russian Acad Sci, Inst Informat Transmiss Problems, Moscow 127994, Russia
[3] Int Ctr Genet Engn & Biotechnol, I-34012 Trieste, Italy
[4] State Res Ctr GosNIIGenet, Moscow 117545, Russia
关键词
D O I
10.1016/j.molcel.2005.06.035
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 plays a key role in generating protein diversity. Transfections with minigenes; revealed coordination between two distant, alternatively spliced exons in the same gene. Mutations that either inhibit or stimulate inclusion of the upstream alternative exon deeply affect inclusion of the downstream one. However, similar mutations at the downstream alternative exon have little effect on the upstream one. This polar effect is promoter specific and is enhanced by inhibition of transcriptional elongation. Consistently, cells from mutant mice with either constitutive or null inclusion of a fibronectin alternative exon revealed coordination with a second alternative splicing region, located far downstream. Using allele-specific RT-PCR, we demonstrate that this coordination occurs in cis and is also affected by transcriptional elongation rates. Bioinformatics supports the generality of these findings, indicating that 25% of human genes contain multiple alternative splicing regions and identifying several genes with nonrandom distribution of mRNA isoforms at two alternative regions.
引用
收藏
页码:393 / 404
页数:12
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