首页> 外文OA文献 >Serine- and Arginine-rich Proteins 55 and 75 (SRp55 and SRp75) Induce Production of HIV-1 vpr mRNA by Inhibiting the 5′-Splice Site of Exon 3
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Serine- and Arginine-rich Proteins 55 and 75 (SRp55 and SRp75) Induce Production of HIV-1 vpr mRNA by Inhibiting the 5′-Splice Site of Exon 3

机译:富含丝氨酸和精氨酸的蛋白质55和75(SRp55和SRp75)通过抑制外显子3'的5'-剪接位点来诱导HIV-1 vpr mRNA的产生。

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摘要

HIV-1 non-coding exon 3 can either be spliced to exons 4, 4a, 4b, 4c, and 5 to generate tat, rev, and nef mRNAs or remain unspliced to produce the 13a7 vpr mRNA. Here we show that serine- and arginine-rich proteins 55 and 75 (SRp55 and SRp75) inhibit splicing from the 5′-splice site of exon 3 thereby causing an accumulation of the partially unspliced 13a7 vpr mRNA. In contrast, serine- and arginine-rich protein 40 (SRp40) induces splicing from exon 3 to exon 4, thereby promoting the production of the 1347 tat mRNA. We demonstrate that SRp55 stimulates vpr mRNA production by interacting with the previously identified HIV-1 splicing enhancer named GAR and inhibiting its function. This inhibition requires both serine arginine-rich and RNA-binding domains of SRp55, indicating that production of HIV-1 vpr mRNA depends on the interaction of SRp55 with an unknown factor.
机译:HIV-1非编码外显子3可以剪接至外显子4、4a,4b,4c和5,以产生tat,rev和nef mRNA,或者不剪接以产生13a7 vpr mRNA。在这里,我们显示富含丝氨酸和精氨酸的蛋白55和75(SRp55和SRp75)可抑制来自外显子3的5'剪接位点的剪接,从而引起部分未剪接的13a7 vpr mRNA的积累。相反,富含丝氨酸和精氨酸的蛋白质40(SRp40)诱导从外显子3到外显子4的剪接,从而促进了1347 tat mRNA的产生。我们证明,SRp55通过与先前确定的名为GAR的HIV-1剪接增强子相互作用并抑制其功能来刺激vpr mRNA的产生。这种抑制需要SRp55的富含丝氨酸的精氨酸和RNA结合域,这表明HIV-1 vpr mRNA的产生取决于SRp55与未知因子的相互作用。

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