Rodriguez Jose M, Glozak Michele A, Ma Yihong, Cress W Douglas
Molecular Oncology Program, H. Lee Moffitt Cancer Center and Research Institute, Department of Interdisciplinary Oncology, Cancer Biology Ph.D. Program, University of South Florida, Tampa, Florida 33612.
J Biol Chem. 2006 Aug 11;281(32):22729-35. doi: 10.1074/jbc.M604705200. Epub 2006 Jun 13.
Bok/Mtd (Bcl-2-related ovarian killer/Matador) is considered a pro-apoptotic member of the Bcl-2 family. Although identified in 1997, little is known about its biological role. We have previously demonstrated that Bok mRNA is up-regulated following E2F1 overexpression. In the current work, we demonstrate that Bok RNA is low in quiescent cells and rises upon serum stimulation. To determine the mechanism underlying this regulation, we cloned and characterized the mouse Bok promoter. We find that the mouse promoter contains a conserved E2F binding site (-43 to -49) and that a Bok promoter-driven luciferase reporter is activated by serum stimulation dependent on this site. Chromatin immunoprecipitation assays demonstrate that endogenous E2F1 and E2F3 associate with the Bok promoter in vivo. Surprisingly, we find that H1299 cells can stably express high levels of exogenous Bok protein. However, these cells are highly sensitive to chemotherapeutic drug treatment. Taken together these results demonstrate that Bok represents a cell cycle-regulated pro-apoptotic member of the Bcl-2 family, which may predispose growing cells to chemotherapeutic treatment.
Bok/Mtd(Bcl-2相关卵巢杀手/杀手)被认为是Bcl-2家族的促凋亡成员。尽管它于1997年被发现,但其生物学作用却鲜为人知。我们之前已经证明,在E2F1过表达后Bok mRNA会上调。在当前的研究中,我们证明Bok RNA在静止细胞中含量较低,而在血清刺激后会升高。为了确定这种调控的潜在机制,我们克隆并鉴定了小鼠Bok启动子。我们发现小鼠启动子包含一个保守的E2F结合位点(-43至-49),并且一个由Bok启动子驱动的荧光素酶报告基因在血清刺激下会依赖于该位点被激活。染色质免疫沉淀分析表明内源性E2F1和E2F3在体内与Bok启动子相关联。令人惊讶的是,我们发现H1299细胞能够稳定表达高水平的外源性Bok蛋白。然而,这些细胞对化疗药物治疗高度敏感。综合这些结果表明,Bok代表了Bcl-2家族中一个受细胞周期调控的促凋亡成员,这可能使生长中的细胞更容易受到化疗治疗。