Berger K H, Yaffe M P
Department of Biology, University of California, San Diego, La Jolla, California, USA.
Mol Cell Biol. 1998 Jul;18(7):4043-52. doi: 10.1128/MCB.18.7.4043.
Phb2p, a homolog of the tumor suppressor protein prohibitin, was identified in a genetic screen for suppressors of the loss of Mdm12p, a mitochondrial outer membrane protein required for normal mitochondrial morphology and inheritance in Saccharomyces cerevisiae. Phb2p and its homolog, prohibitin (Phb1p), were localized to the mitochondrial inner membrane and characterized as integral membrane proteins which depend on each other for their stability. In otherwise wild-type genetic backgrounds, null mutations in PHB1 and PHB2 did not confer any obvious phenotypes. However, loss of function of either PHB1 or PHB2 in cells with mitochondrial DNA deleted led to altered mitochondrial morphology, and phb1 or phb2 mutations were synthetically lethal when combined with a mutation in any of three mitochondrial inheritance components of the mitochondrial outer membrane, Mdm12p, Mdm10p, and Mmm1p. These results provide the first evidence of a role for prohibitin in mitochondrial inheritance and in the regulation of mitochondrial morphology.
Phb2p是肿瘤抑制蛋白禁止素的同源物,它是在一项基因筛选中被鉴定出来的,该筛选旨在寻找Mdm12p缺失的抑制因子,Mdm12p是酿酒酵母中正常线粒体形态和遗传所必需的线粒体外膜蛋白。Phb2p及其同源物禁止素(Phb1p)定位于线粒体内膜,并被表征为相互依赖以维持稳定性的整合膜蛋白。在其他方面为野生型的遗传背景下,PHB1和PHB2的无效突变并未赋予任何明显的表型。然而,在缺失线粒体DNA的细胞中,PHB1或PHB2功能丧失会导致线粒体形态改变,并且当phb1或phb2突变与线粒体外膜的三个线粒体遗传成分Mdm12p、Mdm10p和Mmm1p中的任何一个突变结合时,会产生合成致死效应。这些结果首次证明了禁止素在线粒体遗传和线粒体形态调节中的作用。