首页> 外文期刊>Nucleic Acids Research >Tissue-specific splicing regulator Fox-1 induces exon skipping by interfering E complex formation on the downstream intron of human F1 gamma gene
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Tissue-specific splicing regulator Fox-1 induces exon skipping by interfering E complex formation on the downstream intron of human F1 gamma gene

机译:组织特异性剪接调节因子Fox-1通过干扰人类F1γ基因下游内含子上的E复合物形成诱导外显子跳跃

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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.
机译:Fox-1通过与肌肉和神经元细胞中mRNA前体中的元素(U)GCAUG结合,是组织特异性剪接的调节剂。 Fox-1可以正向或负向调节剪接,最可能取决于它相对于被调节外显子的结合位置。在(U)GCAUG元件位于替代外显子上游的内含子中的情况下,Fox-1蛋白可作为剪接阻遏物来诱导外显子跳跃。在这里,我们报告使用hF1伽玛基因作为模型系统,受Fox-1调控的外显子跳跃机制。我们发现Fox-1通过与位于上游内含子8的GCAUG阻遏物结合,通过抑制下游内含子9的剪接来诱导外显子9跳跃。体外剪接分析表明Fox-1阻止了早期剪接体的形成( E)内含子9上的复合物。此外,我们定位了诱导外显子跳跃所需的Fox-1蛋白区域。综上所述,我们的数据显示了RNA结合蛋白如何调控选择性剪接的新机制。

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