Ward A, Pooler J A, Miyagawa K, Duarte A, Hastie N D, Caricasole A
Department of Zoology, University of Oxford, UK.
Gene. 1995 Dec 29;167(1-2):239-43. doi: 10.1016/0378-1119(95)00645-1.
We have investigated actions of the Wilms' tumour suppressor zinc finger transcription factor, WT1, on promoters of the mouse insulin-like growth factor II-encoding gene (Igf-2). Two variant forms of WT1 repressed the two major Igf-2 promoters (P2 and P3) in transient transfection assays. WT1-binding sites were characterised in both these promoters and in the transcribed region downstream from P2, exon 2. In each of these regions, there was a pair of WT1-binding sites, and mutational analysis of the exon-2 sites indicated that both were required for full repression. Cooperative binding of WT1 to these sites might explain the dominant-negative mutations of WT1 observed in some Wilms' tumours and Denys-Drash syndrome cases.
我们研究了肾母细胞瘤抑制锌指转录因子WT1对小鼠胰岛素样生长因子II编码基因(Igf-2)启动子的作用。在瞬时转染实验中,两种变异形式的WT1抑制了两个主要的Igf-2启动子(P2和P3)。在这两个启动子以及P2下游的转录区域外显子2中鉴定出了WT1结合位点。在这些区域的每一个中,都有一对WT1结合位点,对外显子2位点的突变分析表明,两者对于完全抑制都是必需的。WT1与这些位点的协同结合可能解释了在一些肾母细胞瘤和Denys-Drash综合征病例中观察到的WT1显性负性突变。