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剪接因子Sub2p通过与Yra1p相互作用,对核mRNA输出是必需的。

Splicing factor Sub2p is required for nuclear mRNA export through its interaction with Yra1p.

作者信息

Strässer K, Hurt E

机构信息

BZH--Biochemie-Zentrum Heidelberg, Im Neuenheimer Feld 328, D-69120 Heidelberg, Germany.

出版信息

Nature. 2001 Oct 11;413(6856):648-52. doi: 10.1038/35098113.

Abstract

The yeast nuclear protein Yra1p is an essential export factor for mRNA. Yra1p interacts directly with the mRNA transport factor Mex67p/Mtr2p, which is associated with the nuclear pore. Here, we report a genetic interaction between YRA1 and SUB2, the gene for a DEAD box helicase involved in splicing. Mutation of SUB2 as well as its overexpression leads to a defect in mRNA export. Moreover, Yra1p and Sub2p bind directly to each other both in vivo and in vitro. Significantly, Sub2p and Mex67p/Mtr2p bind to the same domains of Yra1p, and the proteins compete for binding to Yra1p. Together, these data indicate that the spliceosomal component Sub2p is also important in mRNA export and may function to recruit Yra1p to the mRNA. Sub2p may then be displaced from Yra1p by the binding of Mex67p/Mtr2p, which participates in the export of mRNA through the nuclear pores.

摘要

酵母核蛋白Yra1p是mRNA的一种必需输出因子。Yra1p直接与mRNA转运因子Mex67p/Mtr2p相互作用,后者与核孔相关。在此,我们报道了YRA1与SUB2之间的遗传相互作用,SUB2是一个参与剪接的DEAD盒解旋酶的基因。SUB2的突变及其过表达均导致mRNA输出缺陷。此外,Yra1p和Sub2p在体内和体外均直接相互结合。重要的是,Sub2p和Mex67p/Mtr2p与Yra1p的相同结构域结合,并且这两种蛋白竞争与Yra1p的结合。总之,这些数据表明剪接体成分Sub2p在mRNA输出中也很重要,并且可能起到将Yra1p招募到mRNA上的作用。然后,Mex67p/Mtr2p的结合可能会使Sub2p从Yra1p上被取代,Mex67p/Mtr2p参与mRNA通过核孔的输出。

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