Zwiller J, Sassone-Corsi P, Kakazu K, Boynton A L
Centre de Neurochimie, CNRS, Strasbourg, France.
Oncogene. 1991 Feb;6(2):219-21.
The expression of the proto-oncogenes c-fos, c-jun, jun B and jun D was monitored in quiescent C3H10T1/2 fibroblasts after stimulation with PDGF. The mRNA level of c-fos, c-jun and jun B, but not of jun D, was stimulated by PDGF. The inductions were abolished when genistein, a specific tyrosine protein kinase inhibitor, was added concomitantly with PDGF, a condition in which DNA synthesis is known to be inhibited. As already shown previously, treatment with PDGF and genistein for 4h followed by the replacement with fresh medium induces the progression of the cells through the G1 phase of their growth-division cycle, without phospholipase C activation. The removal of PDGF and genistein was accompanied by an important increase in c-fos, c-jun and jun B mRNA expression, which correlated with the entrance of cells into G1 phase. Thus, the proto-oncogene expressions induced by PDGF are also obtained in the absence of phospholipase C activation. This result also suggests that the mRNA levels of c-jun, jun B and to a lesser degree c-fos are positively regulated by tyrosine protein kinase activity, whereas jun D is negatively regulated.
在用血小板衍生生长因子(PDGF)刺激静止的C3H10T1/2成纤维细胞后,监测原癌基因c-fos、c-jun、jun B和jun D的表达情况。PDGF刺激了c-fos、c-jun和jun B的mRNA水平,但未刺激jun D的mRNA水平。当在加入PDGF的同时加入特异性酪氨酸蛋白激酶抑制剂染料木黄酮时,诱导作用被消除,已知这种情况下DNA合成会受到抑制。如先前已表明的,用PDGF和染料木黄酮处理4小时,然后换成新鲜培养基,可诱导细胞通过其生长分裂周期的G1期进展,而不激活磷脂酶C。去除PDGF和染料木黄酮后,c-fos、c-jun和jun B的mRNA表达显著增加,这与细胞进入G1期相关。因此,在没有磷脂酶C激活的情况下也能获得由PDGF诱导的原癌基因表达。该结果还表明,c-jun、jun B的mRNA水平以及程度较轻的c-fos的mRNA水平受酪氨酸蛋白激酶活性的正向调节,而jun D受负向调节。