Tissue-specific splicing regulator Fox-1 induces exon skipping by interfering E complex formation on the downstream intron of human F1γ gene

被引:36
作者
Fukumura, Kazuhiro
Kato, Ayako
Jin, Yui
Ideue, Takashi
Hirose, Tetsuro
Kataoka, Naoyuki
Fujiwara, Toshinobu
Sakamoto, Hiroshi
Inoue, Kunio
机构
[1] Kobe Univ, Dept Biol, Grad Sch Sci, Nada Ku, Kobe, Hyogo 6578501, Japan
[2] Natl Inst Adv Ind Sci & Technol, Biol Informat Res Ctr, Tokyo 1350064, Japan
[3] Kyoto Univ, Inst Virus Res, Kyoto 6068507, Japan
基金
日本学术振兴会;
关键词
D O I
10.1093/nar/gkm569
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
Fox-1 is a regulator of tissue-specific splicing, via binding to the element (U) GCAUG in mRNA precursors, in muscles and neuronal cells. Fox-1 can regulate splicing positively or negatively, most likely depending on where it binds relative to the regulated exon. In cases where the (U) GCAUG element lies in an intron upstream of the alternative exon, Fox-1 protein functions as a splicing repressor to induce exon skipping. Here we report the mechanism of exon skipping regulated by Fox-1, using the hF1 gamma gene as a model system. We found that Fox-1 induces exon 9 skipping by repressing splicing of the downstream intron 9 via binding to the GCAUG repressor elements located in the upstream intron 8. In vitro splicing analyses showed that Fox-1 prevents formation of the pre-spliceosomal early (E) complex on intron 9. In addition, we located a region of the Fox-1 protein that is required for inducing exon skipping. Taken together, our data show a novel mechanism of how RNA-binding proteins regulate alternative splicing.
引用
收藏
页码:5303 / 5311
页数:9
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