Angel P, Pöting A, Mallick U, Rahmsdorf H J, Schorpp M, Herrlich P
Mol Cell Biol. 1986 May;6(5):1760-6. doi: 10.1128/mcb.6.5.1760-1766.1986.
We used nucleic acid hybridization and cDNA cloning techniques to isolate human sequences that respond to the tumor promoter 12-O-tetradecanoylphorbol-13-acetate (TPA). These clones were used as probes to examine changes of gene expression that occurred after the proliferation of exponentially growing primary human fibroblasts was arrested. Transcript levels detected by these probes were increased coordinately by treatment of the cells with UV light, mitomycin C, TPA, or the UV light-induced extracellular protein synthesis-inducing factor EPIF (M. Schorpp, U. Mallick, H. J. Rahmsdorf, and P. Herrlich, Cell 37:861-868, 1984). Proteins coded for by these transcripts were characterized by hybrid-promoted translation and by cDNA sequencing. One of the cDNA clones was homologous to the metallothionein IIa gene, and one set of related clones selected RNA for the secreted TPA-inducible protein XHF1 (U. Mallick, H. J. Rahmsdorf, N. Yamamoto, H. Ponta, R.-D. Wegner, and P. Herrlich, Proc. Natl. Acad. Sci. USA 79:7886-7890, 1982).
我们运用核酸杂交和cDNA克隆技术来分离对肿瘤启动子12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA)产生反应的人类序列。这些克隆被用作探针,以检测指数生长的原代人成纤维细胞增殖停止后发生的基因表达变化。用紫外线、丝裂霉素C、TPA或紫外线诱导的细胞外蛋白质合成诱导因子EPIF(M. Schorpp、U. Mallick、H. J. Rahmsdorf和P. Herrlich,《细胞》37:861 - 868,1984)处理细胞后,这些探针检测到的转录水平会协同增加。通过杂交促进翻译和cDNA测序对这些转录本编码的蛋白质进行了表征。其中一个cDNA克隆与金属硫蛋白IIa基因同源,一组相关克隆选择了分泌型TPA诱导蛋白XHF1的RNA(U. Mallick、H. J. Rahmsdorf、N. Yamamoto、H. Ponta、R.-D. Wegner和P. Herrlich,《美国国家科学院院刊》79:7886 - 7890,1982)。