Kasashima Katsumi, Ohta Eriko, Kagawa Yasuo, Endo Hitoshi
Department of Biochemistry, Jichi Medical University, 3311-1 Yakushiji, Shimotsuke, Tochigi 329-0498, Japan.
J Biol Chem. 2006 Nov 24;281(47):36401-10. doi: 10.1074/jbc.M605260200. Epub 2006 Sep 28.
Proteins with multiple cellular functions provide biological diversity to eukaryotic cells. In the current studies, we identified the mitochondrial functions of human prohibitin 2 (PHB2), which was initially identified as a repressor of estrogen-dependent transcriptional activity. The mitochondrial complex of PHB2 consists of PHB1, voltage-dependent anion channel 2, adenine nucleotide translocator 2, and the anti-apoptotic Hax-1, which is a novel binding partner for PHB2. RNA interference-mediated knockdown of PHB2 in HeLa cells resulted in caspase-dependent apoptosis through down-regulation of Hax-1 and fragmentation of mitochondria. We also found that, although PHB2 is predominantly expressed in the mitochondria of HeLa cells, it translocates to nucleus in the presence of estrogen receptor alpha and estradiol. Here, we first demonstrated the roles of mammalian PHB2 in mitochondria and the molecular mechanism of its nuclear targeting and showed that PHB2 is a possible molecule directly coupling nuclear-mitochondrial interaction.
具有多种细胞功能的蛋白质为真核细胞提供了生物多样性。在当前的研究中,我们确定了人类抑制素2(PHB2)的线粒体功能,它最初被鉴定为雌激素依赖性转录活性的抑制剂。PHB2的线粒体复合物由PHB1、电压依赖性阴离子通道2、腺嘌呤核苷酸转位酶2和抗凋亡蛋白Hax-1组成,Hax-1是PHB2的新型结合伴侣。RNA干扰介导的HeLa细胞中PHB2的敲低通过下调Hax-1和线粒体碎片化导致半胱天冬酶依赖性凋亡。我们还发现,尽管PHB2主要在HeLa细胞的线粒体中表达,但在雌激素受体α和雌二醇存在的情况下,它会转移到细胞核中。在这里,我们首次证明了哺乳动物PHB2在线粒体中的作用及其核靶向的分子机制,并表明PHB2是直接连接核-线粒体相互作用的可能分子。