Rabin M S, Doherty P J, Gottesman M M
Proc Natl Acad Sci U S A. 1986 Jan;83(2):357-60. doi: 10.1073/pnas.83.2.357.
Treatment of mouse NIH 3T3 cells with the phorbol ester tumor promoter, phorbol 12-myristate 13-acetate, results in altered transcription of several genes as measured in nuclear run-off experiments. The first set of genes, whose altered transcription occurs rapidly in the absence of protein synthesis, is typified by induction of c-myc and c-fos and decreased transcription of alpha 2 type I procollagen. This work demonstrates the existence of a second class of genes whose rapidly increased transcription requires prior protein synthesis, which is represented by the gene encoding a secreted lysosomal protein, MEP. Similar induction of MEP RNA is seen after treatment with platelet-derived growth factor or transformation with Kirsten sarcoma virus.
用佛波酯肿瘤启动子佛波醇12 -肉豆蔻酸酯13 -乙酸酯处理小鼠NIH 3T3细胞,在核延伸实验中检测到几种基因的转录发生改变。第一组基因,其转录改变在无蛋白质合成的情况下迅速发生,以c - myc和c - fos的诱导以及α2 I型前胶原转录减少为典型。这项研究证明存在第二类基因,其转录迅速增加需要先有蛋白质合成,这以编码分泌性溶酶体蛋白MEP的基因作为代表。在用血小板衍生生长因子处理或用柯斯顿肉瘤病毒转化后,可观察到MEP RNA有类似的诱导情况。