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WT1在剪接或转录因子结构域中的亚核定位受可变剪接调控。

Subnuclear localization of WT1 in splicing or transcription factor domains is regulated by alternative splicing.

作者信息

Larsson S H, Charlieu J P, Miyagawa K, Engelkamp D, Rassoulzadegan M, Ross A, Cuzin F, van Heyningen V, Hastie N D

机构信息

Medical Research Council Human Genetics Unit, Western General Hospital, Edinburgh, Scotland.

出版信息

Cell. 1995 May 5;81(3):391-401. doi: 10.1016/0092-8674(95)90392-5.

Abstract

WT1 is a tumor suppressor gene with a key role in urogenital development and the pathogenesis of Wilms' tumor. Two alternative splice sites in the WT1 transcript allow the gene to encode four proteins. These carry four Krüppel-type zinc fingers and to date have primarily been implicated in transcriptional control of genes involved in growth regulation. However, here we demonstrate colocalization of WT1 with splicing factors in the fetal kidney and testis and in expressing cell lines. Using immunoprecipitation, we show that two WT1 isoforms directly associate with one or a limited number of components in the spliceosomes and coiled bodies. Moreover, COS cell expression studies suggest that alternative splicing within the WT1 zinc finger region determines whether the protein localizes mainly with splicing factors or with DNA in transcription factor domains in the nucleus. We propose that WT1 plays roles in posttranscriptional processing of RNA as well as in transcription.

摘要

WT1是一种肿瘤抑制基因,在泌尿生殖系统发育和肾母细胞瘤的发病机制中起关键作用。WT1转录本中的两个可变剪接位点使该基因能够编码四种蛋白质。这些蛋白质带有四个克鲁ppel型锌指,迄今为止主要参与了与生长调节相关基因的转录调控。然而,我们在此证明了WT1在胎儿肾脏和睾丸以及表达细胞系中与剪接因子共定位。通过免疫沉淀,我们表明两种WT1异构体直接与剪接体和卷曲体中的一种或有限数量的成分相关联。此外,COS细胞表达研究表明,WT1锌指区域内的可变剪接决定了该蛋白质主要定位于剪接因子还是细胞核中转录因子结构域中的DNA。我们提出,WT1在RNA的转录后加工以及转录过程中均发挥作用。

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