Rauscher F J, Cohen D R, Curran T, Bos T J, Vogt P K, Bohmann D, Tjian R, Franza B R
Roche Institute for Molecular Biology, Nutley, NJ 07110.
Science. 1988 May 20;240(4855):1010-6. doi: 10.1126/science.3130660.
The Fos protein complex and several Fos-related antigens (FRA) bind specifically to a sequence element referred to as the HeLa cell activator protein 1 (AP-1) binding site. A combination of structural and immunological comparisons has identified the Fos-associated protein (p39) as the protein product of the jun proto-oncogene (c-Jun). The p39/Jun protein is one of the major polypeptides identified in AP-1 oligonucleotide affinity chromatography extracts of cellular proteins. These preparations of AP-1 also contain Fos and several FRA's. Some of these proteins bind to the AP-1 site directly whereas others, like Fos, appear to bind indirectly via protein-protein interactions. Cell-surface stimulation results in an increase in c-fos and c-jun products. Thus, the products of two protooncogenes (and several related proteins), induced by extracellular stimuli, form a complex that associates with transcriptional control elements containing AP-1 sites, thereby potentially mediating the long-term responses to signals that regulate growth control and development.
Fos蛋白复合体和几种Fos相关抗原(FRA)特异性结合于一种被称为HeLa细胞激活蛋白1(AP-1)结合位点的序列元件。结构和免疫学比较相结合已确定Fos相关蛋白(p39)为原癌基因jun(c-Jun)的蛋白质产物。p39/Jun蛋白是在细胞蛋白质的AP-1寡核苷酸亲和层析提取物中鉴定出的主要多肽之一。这些AP-1制剂还含有Fos和几种FRA。其中一些蛋白质直接结合到AP-1位点,而其他一些蛋白质,如Fos,似乎通过蛋白质-蛋白质相互作用间接结合。细胞表面刺激导致c-fos和c-jun产物增加。因此,由细胞外刺激诱导的两个原癌基因的产物(以及几种相关蛋白质)形成一个复合体,该复合体与含有AP-1位点的转录控制元件相关联,从而可能介导对调节生长控制和发育的信号的长期反应。