Yoshida Kiyotsugu, Yamaguchi Tomoko, Shinagawa Hirokuni, Taira Naoe, Nakayama Keiichi I, Miki Yoshio
Department of Molecular Genetics, Medical Research Institute, Tokyo Medical and Dental University, 1-5-45, Yushima, Bunkyo-ku, Tokyo 113-8510, Japan.
Mol Cell Biol. 2006 May;26(9):3414-31. doi: 10.1128/MCB.26.9.3414-3431.2006.
DNA topoisomerase II is an essential nuclear enzyme that modulates DNA processes by altering the topological state of double-stranded DNA. This enzyme is required for chromosome condensation and segregation; however, the regulatory mechanism of its activation is largely unknown. Here we demonstrate that topoisomerase IIalpha is activated in response to genotoxic stress. Concomitant with the activation, the expression of topoisomerase IIalpha is increased following DNA damage. The results also demonstrate that the proapoptotic kinase protein kinase C delta (PKCdelta) interacts with topoisomerase IIalpha. This association is in an S-phase-specific manner and is required for stabilization and catalytic activation of topoisomerase IIalpha in response to DNA damage. Conversely, inhibition of PKCdelta activity attenuates DNA damage-induced activation of topoisomerase IIalpha. Finally, aberrant activation of topoisomerase IIalpha by PKCdelta is associated with induction of apoptosis upon exposure to genotoxic agents. These findings indicate that PKCdelta regulates topoisomerase IIalpha and thereby cell fate in the genotoxic stress response.
DNA拓扑异构酶II是一种必需的核酶,通过改变双链DNA的拓扑状态来调节DNA进程。这种酶对于染色体浓缩和分离是必需的;然而,其激活的调控机制在很大程度上尚不清楚。在这里,我们证明拓扑异构酶IIα响应基因毒性应激而被激活。伴随着激活,DNA损伤后拓扑异构酶IIα的表达增加。结果还表明,促凋亡激酶蛋白激酶Cδ(PKCδ)与拓扑异构酶IIα相互作用。这种关联以S期特异性方式存在,并且是DNA损伤响应中拓扑异构酶IIα稳定化和催化激活所必需的。相反,抑制PKCδ活性会减弱DNA损伤诱导的拓扑异构酶IIα激活。最后,PKCδ异常激活拓扑异构酶IIα与暴露于基因毒性剂后诱导细胞凋亡有关。这些发现表明,PKCδ在基因毒性应激反应中调节拓扑异构酶IIα,从而调控细胞命运。