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The splicing factor SF2/ASF regulates translation initiation by enhancing phosphorylation of 4E-BP1

机译:剪接因子SF2 / ASF通过增强4E-BP1的磷酸化来调节翻译起始

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摘要

The SIR protein SF2/ASF has been initially characterized as a splicing factor but has also been shown to mediate postsplicing activities such as mRNA export and translation. Here we demonstrate that SF2/ASF promotes translation initiation of bound mRNAs and that this activity requires the presence of the cytoplasmic cap-binding protein elF4E. SF2/ASF promotes translation initiation by suppressing the activity of 4E-BP, acompetitive inhibitor of cap-dependent translation. This activity is mediated by interactions of SF2/ASF with both mTOR and the phosphatase PP2A, two key regulators of 4E-BP phosphorylation. These findings suggest the model whereby SF2/ ASF functions as an adaptor protein to recruit the signaling molecules responsible for regulation of cap-dependent translation of specific mRNAs. Taken together, these data suggest a novel mechanism for the activation of translation initiation of a subset of mRNAs bound by the shuttling protein SF2/ASF.
机译:SIR蛋白SF2 / ASF最初已被表征为剪接因子,但也已显示出介导剪接后的活性,例如mRNA输出和翻译。在这里,我们证明SF2 / ASF促进结合的mRNA的翻译起始,并且这种活性需要细胞质帽结合蛋白elF4E的存在。 SF2 / ASF通过抑制4E-BP(帽依赖性翻译的竞争性抑制剂)的活性来促进翻译起始。 SF2 / ASF与mTOR和磷酸酶PP2A(4E-BP磷酸化的两个关键调节因子)的相互作用介导了该活性。这些发现提示了SF2 / ASF充当衔接子蛋白来募集负责调节特定mRNA帽依赖性翻译的信号传导分子的模型。综上所述,这些数据提出了一种新的机制,用于激活由穿梭蛋白SF2 / ASF结合的一部分mRNA的翻译起始。

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