Fukumura Kazuhiro, Kato Ayako, Jin Yui, Ideue Takashi, Hirose Tetsuro, Kataoka Naoyuki, Fujiwara Toshinobu, Sakamoto Hiroshi, Inoue Kunio
Department of Biology, Graduate School of Science, Kobe University, 1-1 Rokkodaicho, Nadaku, Kobe 657-8501, Japan.
Nucleic Acids Res. 2007;35(16):5303-11. doi: 10.1093/nar/gkm569. Epub 2007 Aug 7.
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 hF1gamma 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.
Fox-1是一种组织特异性剪接的调节因子,它通过与肌肉和神经细胞中mRNA前体的(U)GCAUG元件结合来发挥作用。Fox-1可以正向或负向调节剪接,这很可能取决于它相对于受调节外显子的结合位置。当(U)GCAUG元件位于可变外显子上游的内含子中时,Fox-1蛋白作为剪接抑制因子发挥作用,诱导外显子跳跃。在此,我们以hF1gamma基因为模型系统,报道了由Fox-1调节的外显子跳跃机制。我们发现,Fox-1通过与位于上游内含子8中的GCAUG抑制元件结合,抑制下游内含子9的剪接,从而诱导外显子9跳跃。体外剪接分析表明,Fox-1可阻止内含子9上剪接体早期(E)复合物的形成。此外,我们还确定了Fox-1蛋白中诱导外显子跳跃所需的一个区域。综上所述,我们的数据揭示了RNA结合蛋白调节可变剪接的一种新机制。