Doniger J, DiPaolo J A
Laboratory of Biology, National Cancer Institute, Bethesda, MD 20892.
Nucleic Acids Res. 1988 Feb 11;16(3):969-80. doi: 10.1093/nar/16.3.969.
Tumorigenic guinea pig cell lines with mutationally activated N-ras alleles also exhibited up-regulated N-ras mRNA. Mutational activation and mRNA up-regulation were limited to tumorigenic cells; preneoplastic progenitors were unaffected. Therefore, up-regulation occurred at a late stage of carcinogenesis closely associated with acquisition of tumorigenicity. cDNA and S1 protection analysis demonstrated that polyadenylation site of the short N-ras message and the mRNA start sites were different from that reported for human. The promoter region contained no canonical TATA or CCAAT boxes, but exhibited GGGCGG and CCGCCC SPl binding motifs characteristic of growth control genes. Moreover, both mutant and wild-type alleles were up-regulated in a guinea pig line heterozygous for N-ras codon 61. Coordinate N-ras mutational activation and up-regulation in five independent tumorigenic lines with unique chromosome constitutions suggests that both events are required for expression of the neoplastic phenotype.
具有突变激活的N-ras等位基因的致瘤豚鼠细胞系也表现出N-ras mRNA上调。突变激活和mRNA上调仅限于致瘤细胞;肿瘤前祖细胞未受影响。因此,上调发生在致癌作用的晚期,与致瘤性的获得密切相关。cDNA和S1保护分析表明,短N-ras信息的聚腺苷酸化位点和mRNA起始位点与人类报道的不同。启动子区域不包含典型的TATA或CCAAT框,但具有生长控制基因特有的GGGCGG和CCGCCC SPl结合基序。此外,在N-ras密码子61杂合的豚鼠品系中,突变型和野生型等位基因均上调。在五个具有独特染色体组成的独立致瘤细胞系中,N-ras的协同突变激活和上调表明这两个事件都是肿瘤表型表达所必需的。