Busch Maike, Schwindt Heinrich, Brandt Artur, Beier Manfred, Görldt Nicole, Romaniuk Paul, Toska Eneda, Roberts Stefan, Royer Hans-Dieter, Royer-Pokora Brigitte
Institute of Human Genetics and Anthropology, Heinrich-Heine University, Medical Faculty, Düsseldorf D-40225, Germany.
Institute of Biochemistry and Microbiology, University of Victoria, Victoria, BC, Canada V8P 5C2.
Hum Mol Genet. 2014 Aug 1;23(15):3958-74. doi: 10.1093/hmg/ddu111. Epub 2014 Mar 11.
The WT1 gene encodes a zinc finger transcription factor important for normal kidney development. WT1 is a suppressor for Wilms tumour development and an oncogene for diverse malignant tumours. We recently established cell lines from primary Wilms tumours with different WT1 mutations. To investigate the function of mutant WT1 proteins, we performed WT1 knockdown experiments in cell lines with a frameshift/extension (p.V432fsX87 = Wilms3) and a stop mutation (p.P362X = Wilms2) of WT1, followed by genome-wide gene expression analysis. We also expressed wild-type and mutant WT1 proteins in human mesenchymal stem cells and established gene expression profiles. A detailed analysis of gene expression data enabled us to classify the WT1 mutations as gain-of-function mutations. The mutant WT1(Wilms2) and WT1(Wilms3) proteins acquired an ability to modulate the expression of a highly significant number of genes from the G2/M phase of the cell cycle, and WT1 knockdown experiments showed that they are required for Wilms tumour cell proliferation. p53 negatively regulates the activity of a large number of these genes that are also part of a core proliferation cluster in diverse human cancers. Our data strongly suggest that mutant WT1 proteins facilitate expression of these cell cycle genes by antagonizing transcriptional repression mediated by p53. We show that mutant WT1 can physically interact with p53. Together the findings show for the first time that mutant WT1 proteins have a gain-of-function and act as oncogenes for Wilms tumour development by regulating Wilms tumour cell proliferation.
WT1基因编码一种对正常肾脏发育至关重要的锌指转录因子。WT1是肾母细胞瘤发生的抑制因子,也是多种恶性肿瘤的癌基因。我们最近从具有不同WT1突变的原发性肾母细胞瘤中建立了细胞系。为了研究突变型WT1蛋白的功能,我们在具有WT1移码/延伸(p.V432fsX87 = Wilms3)和终止突变(p.P362X = Wilms2)的细胞系中进行了WT1敲低实验,随后进行全基因组基因表达分析。我们还在人间充质干细胞中表达野生型和突变型WT1蛋白,并建立了基因表达谱。对基因表达数据的详细分析使我们能够将WT1突变分类为功能获得性突变。突变型WT1(Wilms2)和WT1(Wilms3)蛋白获得了调节细胞周期G2/M期大量基因表达的能力,WT1敲低实验表明它们是肾母细胞瘤细胞增殖所必需的。p53负调控大量这些基因的活性,这些基因也是多种人类癌症核心增殖簇的一部分。我们的数据强烈表明,突变型WT1蛋白通过拮抗p53介导的转录抑制来促进这些细胞周期基因的表达。我们表明突变型WT1可以与p53发生物理相互作用。这些发现共同首次表明,突变型WT1蛋白具有功能获得性,并通过调节肾母细胞瘤细胞增殖而作为肾母细胞瘤发生的癌基因。