A vertebrate RNA-binding protein Fox-1 regulates tissue-specific splicing via the pentanucleotide GCAUG

被引:254
作者
Jin, Y
Suzuki, H
Maegawa, S
Endo, H
Sugano, S
Hashimoto, K
Yasuda, K
Inoue, K [1 ]
机构
[1] Nara Inst Sci & Technol, Grad Sch Biol Sci, Ikoma 6300101, Japan
[2] Jichi Med Sch, Dept Biochem, Minamimaki, Tochigi 3290498, Japan
[3] Univ Tokyo, Inst Med Sci, Tokyo 1088639, Japan
[4] Natl Inst Infect Dis, Div Genet Resources, Tokyo 1628640, Japan
关键词
alternative splicing; Fox-1; GCAUG; RNA binding;
D O I
10.1093/emboj/cdg089
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 is one of the central mechanisms that regulate eukaryotic gene expression. Here we report a tissue-specific RNA-binding protein, Fox-1, which regulates alternative splicing in vertebrates. Fox-1 bound specifically to a pentanucleotide GCAUG in vitro. In zebrafish and mouse,fox-1 is expressed in heart and skeletal muscles. As candidates for muscle-specific targets of Fox-1, we considered two genes, the human mitochondrial ATP synthase gamma-subunit gene (Fly) and the rat alpha-actinin gene, because their primary transcripts contain several copies of GCAUG. In transfection experiments, Fox-1 induced muscle-specific exon skipping of the F1gamma gene via binding to GCAUG sequences upstream of the regulated exon. Fox-1 also regulated mutually exclusive splicing of the alpha-actinin gene, antagonizing the repressive effect of polypyrimidine tract-binding protein (PTB). It has been reported that GCAUG is essential for the alternative splicing regulation of several genes including fibronectin. We found that Fox-1 promoted inclusion of the fibronectin EIIIB exon. Thus, we conclude that Fox-1 plays key roles in both positive and negative regulation of tissue-specific splicing via GCAUG.
引用
收藏
页码:905 / 912
页数:8
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