Schütte J, Viallet J, Nau M, Segal S, Fedorko J, Minna J
NCI-Navy Medical Oncology Branch, Bethesda, Maryland.
Cell. 1989 Dec 22;59(6):987-97. doi: 10.1016/0092-8674(89)90755-1.
We have cloned the human jun-B gene and determined its sequence and transforming and trans-activating activities. jun-B is less potent that c-jun in transforming and immortalizing primary rat embryo cells in cooperation with activated ras (effects enhanced by c-fos and TPA); unlike c-jun, jun-B does not transform Rat-1A cells alone. However, cotransfection of c-jun and jun-B into primary rat embryo cells with c-Ha-ras results in a significant decrease in transformation compared with c-jun alone, an event reversed by TPA. Cotransfection of c-jun and jun-B with or without c-fos into F9 teratocarcinoma cells results in decreased trans-activation of AP-1 compared with either gene alone. Introduction of jun-B into primary rat c-jun/ras transformants or c-jun into jun-B/ras transformants also results in a decrease in trans-activation. These findings demonstrate that, whereas jun-B and c-jun each participate in AP-1 trans-activation and malignant transformation, interactions between them involve negative regulation.
我们已经克隆了人类jun - B基因,并确定了其序列以及转化和反式激活活性。与激活的ras共同作用时,jun - B在转化和永生化原代大鼠胚胎细胞方面的效力低于c - jun(c - fos和TPA可增强其作用效果);与c - jun不同,jun - B单独不能转化Rat - 1A细胞。然而,将c - jun和jun - B与c - Ha - ras共转染到原代大鼠胚胎细胞中,与单独转染c - jun相比,转化作用显著降低,TPA可逆转这一现象。将c - jun和jun - B无论有无c - fos共转染到F9畸胎瘤细胞中,与单独转染任一基因相比,AP - 1的反式激活作用均降低。将jun - B导入原代大鼠c - jun/ras转化细胞或把c - jun导入jun - B/ras转化细胞中,也会导致反式激活作用降低。这些发现表明,虽然jun - B和c - jun都参与AP - 1的反式激活和恶性转化,但它们之间的相互作用涉及负调控。