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UAP56与Aly之间的直接相互作用将前体mRNA剪接与mRNA输出联系起来。

Pre-mRNA splicing and mRNA export linked by direct interactions between UAP56 and Aly.

作者信息

Luo M L, Zhou Z, Magni K, Christoforides C, Rappsilber J, Mann M, Reed R

机构信息

Department of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Nature. 2001 Oct 11;413(6856):644-7. doi: 10.1038/35098106.

Abstract

Recent studies indicate that splicing of pre-messenger RNA and export of mRNA are normally coupled in vivo. During splicing, the conserved mRNA export factor Aly is recruited to the spliced mRNA-protein complex (mRNP), which targets the mRNA for export. At present, it is not known how Aly is recruited to the spliced mRNP. Here we show that the conserved DEAD-box helicase UAP56, which functions during spliceosome assembly, interacts directly and highly specifically with Aly. Moreover, UAP56 is present together with Aly in the spliced mRNP. Significantly, excess UAP56 is a potent dominant negative inhibitor of mRNA export. Excess UAP56 also inhibits the recruitment of Aly to the spliced mRNP. Furthermore, a mutation in Aly that blocks its interaction with UAP56 prevents recruitment of Aly to the spliced mRNP. These data suggest that the splicing factor UAP56 functions in coupling the splicing and export machineries by recruiting Aly to the spliced mRNP.

摘要

近期研究表明,前体信使核糖核酸(pre-messenger RNA)的剪接与信使核糖核酸(mRNA)的输出在体内通常是偶联的。在剪接过程中,保守的mRNA输出因子Aly被招募到剪接后的mRNA-蛋白质复合物(mRNP)中,该复合物将mRNA作为输出的靶点。目前,尚不清楚Aly是如何被招募到剪接后的mRNP中的。在此我们表明,在剪接体组装过程中发挥作用的保守的DEAD-box解旋酶UAP56与Aly直接且高度特异性地相互作用。此外,UAP56与Aly共同存在于剪接后的mRNP中。重要的是,过量的UAP56是mRNA输出的一种有效的显性负性抑制剂。过量的UAP56还会抑制Aly被招募到剪接后的mRNP中。此外,Aly中阻止其与UAP56相互作用的突变会阻止Aly被招募到剪接后的mRNP中。这些数据表明,剪接因子UAP56通过将Aly招募到剪接后的mRNP中,在偶联剪接和输出机制中发挥作用。

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