Institut für Zellbiologie, Universität Bayreuth, Germany.
J Cell Biol. 2011 Aug 8;194(3):473-88. doi: 10.1083/jcb.201012088. Epub 2011 Aug 1.
The inheritance of mitochondria in yeast depends on bud-directed transport along actin filaments. It is a matter of debate whether anterograde mitochondrial movement is mediated by the myosin-related motor protein Myo2 or by motor-independent mechanisms. We show that mutations in the Myo2 cargo binding domain impair entry of mitochondria into the bud and are synthetically lethal with deletion of the YPT11 gene encoding a rab-type guanosine triphosphatase. Mitochondrial distribution defects and synthetic lethality were rescued by a mitochondria-specific Myo2 variant that carries a mitochondrial outer membrane anchor. Furthermore, immunoelectron microscopy revealed Myo2 on isolated mitochondria. Thus, Myo2 is an essential and direct mediator of bud-directed mitochondrial movement in yeast. Accumulating genetic evidence suggests that maintenance of mitochondrial morphology, Ypt11, and retention of mitochondria in the bud contribute to Myo2-dependent inheritance of mitochondria.
酵母中线粒体的遗传依赖于沿着肌动蛋白丝向芽部定向的运输。目前仍存在争议,即正向线粒体运动是由肌球蛋白相关的运动蛋白 Myo2 还是由非运动依赖机制介导的。我们表明,Myo2 货物结合域的突变会损害线粒体进入芽部的能力,并且与编码 rab 型鸟苷三磷酸酶的 YPT11 基因缺失具有合成致死性。线粒体特异性 Myo2 变体带有线粒体外膜锚定,可挽救线粒体分布缺陷和合成致死性。此外,免疫电子显微镜显示 Myo2 存在于分离的线粒体上。因此,Myo2 是酵母中线粒体向芽部定向运动的必需且直接的介质。越来越多的遗传证据表明,线粒体形态的维持、Ypt11 和线粒体在芽部的保留有助于 Myo2 依赖的线粒体遗传。