Wilms的肿瘤抑制基因WT1在剪接和转录中都起作用吗?

J P Charlieu, S Larsson, K Miyagawa, V van Heyningen, N D Hastie
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引用次数: 13

摘要

Wilms肿瘤抑制基因(WT1)编码一种具有4个锌指的蛋白质,这对泌尿生殖系统的发育至关重要。大量证据支持WT1结合DNA并作为转录因子发挥作用的观点。然而,我们最近通过共聚焦显微镜和免疫沉淀研究表明,在肾细胞系、胎儿组织和转染的Cos细胞中,WT1的很大一部分与剪接因子有关。WT1的不同同工异构体是由另一种剪接产生的,这种剪接导致锌指3和锌指4之间存在或不存在3个氨基酸插入(KTS)。我们已经证明,这些不同的形式在细胞核中的位置不同。+KTS形式主要定位于剪接因子,-KTS形式主要定位于转录因子。在这里,我们提出了一个模型来解释这些不同的本地化。此外,我们还讨论了这些发现的可能意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Does the Wilms' tumour suppressor gene, WT1, play roles in both splicing and transcription?

The Wilms' tumour suppressor gene (WT1) encodes a protein(s) with 4 zinc fingers that is essential for the development of the genitourinary system. A considerable body of evidence exists to support the idea that WT1 binds DNA and functions as a transcription factor. However, we have shown recently by confocal microscopy and immunoprecipitation studies that a significant proportion of WT1 is associated with splice factors in kidney cell lines, fetal tissues and transfected Cos cells. Different isoforms of WT1 are produced by an alternative splice that leads to the presence or absence of a 3 amino acid insertion (KTS) between zinc fingers 3 and 4. We have shown that these different forms localise differently in the nucleus. The +KTS form mainly localises with splice factors, the -KTS form mainly with transcription factors. Here we propose a model to account for these different localisations. Also, we discuss the possible significance of these findings.

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