Williams B O, Remington L, Albert D M, Mukai S, Bronson R T, Jacks T
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
Nat Genet. 1994 Aug;7(4):480-4. doi: 10.1038/ng0894-480.
The tumour suppressor genes Rb and p53 are mutated in several types of human cancer, and many tumour types carry mutations in both genes. To study how these genes normally function, we and others have created mouse strains with Rb and p53 mutations. Here we describe the phenotypic effects of combined germline mutations in these two tumour suppressor genes. Mice mutant for both genes have reduced viability and exhibit novel pathology including pinealoblastomas, islet cell tumours, bronchial epithelial hyperplasia and retinal dysplasia. These data indicate that mutations in Rb and p53 can cooperate in the transformation of certain cell types in the mouse.
肿瘤抑制基因Rb和p53在多种人类癌症中发生突变,并且许多肿瘤类型在这两个基因中都携带突变。为了研究这些基因的正常功能,我们和其他人创建了具有Rb和p53突变的小鼠品系。在这里,我们描述了这两个肿瘤抑制基因联合种系突变的表型效应。两个基因均突变的小鼠生存能力降低,并表现出包括松果体母细胞瘤、胰岛细胞瘤、支气管上皮增生和视网膜发育异常在内的新病理特征。这些数据表明,Rb和p53中的突变可在小鼠某些细胞类型的转化中协同作用。