Institut für Biochemie und Molekularbiologie, ZBMZ, Universität Freiburg, 79104 Freiburg, Germany.
Curr Biol. 2009 Dec 29;19(24):2133-9. doi: 10.1016/j.cub.2009.10.074. Epub 2009 Dec 3.
The biogenesis of mitochondria requires the import of a large number of proteins from the cytosol [1, 2]. Although numerous studies have defined the proteinaceous machineries that mediate mitochondrial protein sorting, little is known about the role of lipids in mitochondrial protein import. Cardiolipin, the signature phospholipid of the mitochondrial inner membrane [3-5], affects the stability of many inner-membrane protein complexes [6-12]. Perturbation of cardiolipin metabolism leads to the X-linked cardioskeletal myopathy Barth syndrome [13-18]. We report that cardiolipin affects the preprotein translocases of the mitochondrial outer membrane. Cardiolipin mutants genetically interact with mutants of outer-membrane translocases. Mitochondria from cardiolipin yeast mutants, as well as Barth syndrome patients, are impaired in the biogenesis of outer-membrane proteins. Our findings reveal a new role for cardiolipin in protein sorting at the mitochondrial outer membrane and bear implications for the pathogenesis of Barth syndrome.
线粒体的生物发生需要从细胞质中导入大量的蛋白质[1,2]。尽管许多研究已经定义了介导线粒体蛋白分拣的蛋白质机器,但对于脂质在线粒体蛋白导入中的作用知之甚少。心磷脂是线粒体内膜的标志性磷脂[3-5],它影响许多内膜蛋白复合物的稳定性[6-12]。心磷脂代谢的扰动会导致 X 连锁的心脏骨骼肌病巴思综合征[13-18]。我们报告说心磷脂会影响线粒体外膜的前体蛋白转运体。心磷脂突变体在遗传上与外膜转运体的突变体相互作用。心磷脂酵母突变体的线粒体以及巴思综合征患者的线粒体在外膜蛋白生物发生中受损。我们的发现揭示了心磷脂在线粒体外膜蛋白分拣中的新作用,这对巴思综合征的发病机制具有重要意义。