Inohara N, Gourley T S, Carrio R, Muñiz M, Merino J, Garcia I, Koseki T, Hu Y, Chen S, Núñez G
Department of Pathology and Comprehensive Cancer Center, The University of Michigan Medical School, Ann Arbor, Michigan 48109, USA.
J Biol Chem. 1998 Dec 4;273(49):32479-86. doi: 10.1074/jbc.273.49.32479.
We have identified and characterized Diva, which is a novel regulator of apoptosis. Sequence analysis revealed that Diva is a member of the Bcl-2 family of proteins containing Bcl-2 homology domain 1, 2, 3, and 4 (BH1, BH2, BH3, and BH4) regions and a carboxyl-terminal hydrophobic domain. The expression of Diva mRNA was detected in multiple embryonic tissues but was restricted to the ovary and testis in adult mice. The expression of Diva promoted the death of 293T, Ramsey, and T47D cells as well as that of primary sensory neurons, indicating that Diva is a proapoptotic protein. Significantly, Diva lacks critical residues in the conserved BH3 region that mediate the interaction between BH3-containing proapoptotic Bcl-2 homologues and their prosurvival binding partners. Consistent with this, Diva did not bind to cellular Bcl-2 family members including Bcl-2, Bcl-XL, Bcl-w, Mcl-1, and A1/Bfl-1. Furthermore, mutants of Diva lacking the BH3 region fully retained their proapoptotic activity, confirming that Diva promotes apoptosis in a BH3-independent manner. Significantly, Diva interacted with a viral Bcl-2 homologue (vBcl-2) encoded by the Kaposi's sarcoma-associated herpesvirus. Consistent with these associations, apoptosis induced by Diva was inhibited by vBcl-2 but not by Bcl-XL. Importantly, Diva interacted with Apaf-1, an adapter molecule that activates caspase-9, a central death protease of the apoptotic pathway. The expression of Diva inhibited the binding of Bcl-XL to Apaf-1, as determined by immunoprecipitation assays. Thus, Diva represents a novel type of proapoptotic Bcl-2 homologue that promotes apoptosis independently of the BH3 region through direct binding to Apaf-1, thus preventing Bcl-XL from binding to the caspase-9 regulator Apaf-1.
我们已经鉴定并表征了Diva,它是一种新型的细胞凋亡调节因子。序列分析表明,Diva是Bcl-2蛋白家族的成员,包含Bcl-2同源结构域1、2、3和4(BH1、BH2、BH3和BH4)区域以及一个羧基末端疏水结构域。在多种胚胎组织中检测到了Diva mRNA的表达,但在成年小鼠中仅限于卵巢和睾丸。Diva的表达促进了293T、Ramsey和T47D细胞以及初级感觉神经元的死亡,表明Diva是一种促凋亡蛋白。值得注意的是,Diva在保守的BH3区域缺乏关键残基,这些残基介导了含BH3的促凋亡Bcl-2同源物与其抗凋亡结合伴侣之间的相互作用。与此一致的是,Diva不与包括Bcl-2、Bcl-XL、Bcl-w、Mcl-1和A1/Bfl-1在内的细胞Bcl-2家族成员结合。此外,缺失BH3区域的Diva突变体完全保留了它们的促凋亡活性,证实Diva以不依赖BH3的方式促进细胞凋亡。值得注意的是,Diva与卡波西肉瘤相关疱疹病毒编码的病毒Bcl-2同源物(vBcl-2)相互作用。与这些关联一致,Diva诱导的细胞凋亡被vBcl-2抑制,但不被Bcl-XL抑制。重要的是,Diva与Apaf-1相互作用,Apaf-1是一种激活caspase-9的衔接分子,caspase-9是凋亡途径的核心死亡蛋白酶。通过免疫沉淀分析确定,Diva的表达抑制了Bcl-XL与Apaf-1的结合。因此,Diva代表了一种新型的促凋亡Bcl-2同源物,它通过直接与Apaf-1结合,独立于BH3区域促进细胞凋亡,从而阻止Bcl-XL与caspase-9调节因子Apaf-1结合。