Gutman A, Wasylyk B
Laboratoire de Génétique Moléculaire des Eucaryotes du CNRS, Unité 184 de Biologie Moléculaire et de Génie Génétique de l'INSERM, Faculté de Médecine, Strasbourg, France.
EMBO J. 1990 Jul;9(7):2241-6. doi: 10.1002/j.1460-2075.1990.tb07394.x.
PEA3 is a transcription factor which binds to the polyoma virus enhancer and whose activity is regulated by the expression of a number of oncogenes. We show here that PEA3 also binds specifically to the collagenase and fos cellular promoters. On the collagenase promoter, PEA3 acts synergistically with AP-1 to achieve maximum levels of transcription activation by 12-O-tetradecanoylphorbol-13-acetate (TPA), and non-nuclear oncoproteins, thereby defining a TPA- and oncogene-responsive unit (TORU). From a comparative study of the collagenase TORU and the analogous polyoma virus TORU, we conclude that both the binding affinity of the PEA3 motif and the spacing between PEA3 and AP-1 modulate transcription activation induced by oncogene expression.
PEA3是一种转录因子,它能与多瘤病毒增强子结合,其活性受多种癌基因表达的调控。我们在此表明,PEA3还能特异性地与胶原酶和fos细胞启动子结合。在胶原酶启动子上,PEA3与AP-1协同作用,通过12-O-十四烷酰佛波醇-13-乙酸酯(TPA)和非核癌蛋白实现最大水平的转录激活,从而定义了一个TPA和癌基因反应单元(TORU)。通过对胶原酶TORU和类似的多瘤病毒TORU的比较研究,我们得出结论,PEA3基序的结合亲和力以及PEA3与AP-1之间的间距均能调节癌基因表达诱导的转录激活。