Coupling of transcription with alternative splicing:: RNA pol II promoters modulate SF2/ASF and 9G8 effects on an exonic splicing enhancer

被引:253
作者
Cramer, P
Cáceres, JF
Cazalla, D
Kadener, S
Muro, AF
Baralle, FE
Kornblihtt, AR
机构
[1] Univ Buenos Aires, Fac Ciencias Exactas & Nat, Dept Ciencias Biol, Lab Fisiol & Biol Mol, RA-1428 Buenos Aires, DF, Argentina
[2] Western Gen Hosp, MRC, Human Genet Unit, Edinburgh EH4 2XU, Midlothian, Scotland
[3] Int Ctr Genet Engn & Biotechnol, I-34012 Trieste, Italy
基金
英国医学研究理事会;
关键词
D O I
10.1016/S1097-2765(00)80372-X
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 mRNA splicing of the fibronectin EDI exon is controlled by a purine-rich exonic splicing enhancer (ESE), postulated as a binding site for SR proteins. By using a transient expression alternative splicing assay combined with promoter swapping, we have demonstrated that the promoter can also control EDI splicing, arguing for coupling between the transcription and splicing machineries. We now report that the SR proteins SF2/ASF and 9G8 stimulate EDI splicing in vivo and that their effect requires an intact EDI ESE. Most importantly, we show that sensitivity to these SR proteins critically depends on the promoter structure, suggesting that the transcription machinery modulates their recruitment to the ESE.
引用
收藏
页码:251 / 258
页数:8
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