Rauscher F J
Wistar Institute of Anatomy and Biology, Philadelphia, Pennsylvania 19104.
FASEB J. 1993 Jul;7(10):896-903.
Alteration of transcription factor function is becoming a common theme in molecular mechanisms of oncogenesis. A recent example of this trend is the isolation and characterization of the chromosome 11p13 Wilms tumor suppressor gene, WT1. The WT1 protein contains a DNA binding domain consisting of four zinc fingers of the Cys2-His2 class and a proline-glutamine rich region capable of regulating transcription. Deletions of the WT1 gene or point mutations which destroy the DNA binding activity of the protein are associated with the development of the pediatric nephroblastoma Wilms tumor and Denys-Drash syndrome. This article reviews the role of WT1 in normal kidney development processes, the known biochemical functions of the protein and the status of identifying target genes regulated by this potentially oncogenic transcription factor.
转录因子功能的改变正成为肿瘤发生分子机制中的一个常见主题。这种趋势的一个最新例子是11号染色体p13区域威尔姆斯肿瘤抑制基因WT1的分离和表征。WT1蛋白包含一个由四个Cys2-His2类锌指组成的DNA结合结构域和一个能够调节转录的富含脯氨酸-谷氨酰胺的区域。WT1基因的缺失或破坏该蛋白DNA结合活性的点突变与儿童肾母细胞瘤威尔姆斯肿瘤和德尼-德拉什综合征的发生有关。本文综述了WT1在正常肾脏发育过程中的作用、该蛋白已知的生化功能以及鉴定受这种潜在致癌转录因子调控的靶基因的现状。