Sesaki H, Jensen R E
Department of Cell Biology and Anatomy, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
J Cell Biol. 1999 Nov 15;147(4):699-706. doi: 10.1083/jcb.147.4.699.
In yeast, mitochondrial division and fusion are highly regulated during growth, mating and sporulation, yet the mechanisms controlling these activities are unknown. Using a novel screen, we isolated mutants in which mitochondria lose their normal structure, and instead form a large network of interconnected tubules. These mutants, which appear defective in mitochondrial division, all carried mutations in DNM1, a dynamin-related protein that localizes to mitochondria. We also isolated mutants containing numerous mitochondrial fragments. These mutants were defective in FZO1, a gene previously shown to be required for mitochondrial fusion. Surprisingly, we found that in dnm1 fzo1 double mutants, normal mitochondrial shape is restored. Induction of Dnm1p expression in dnm1 fzo1 cells caused rapid fragmentation of mitochondria. We propose that dnm1 mutants are defective in the mitochondrial division, an activity antagonistic to fusion. Our results thus suggest that mitochondrial shape is normally controlled by a balance between division and fusion which requires Dnm1p and Fzo1p, respectively.
在酵母中,线粒体的分裂和融合在生长、交配及孢子形成过程中受到高度调控,然而控制这些活动的机制尚不清楚。通过一项新的筛选,我们分离出了线粒体失去正常结构、转而形成由相互连接的小管构成的大网络的突变体。这些看起来线粒体分裂有缺陷的突变体,均在DNM1基因上携带突变,DNM1是一种定位于线粒体的发动蛋白相关蛋白。我们还分离出了含有大量线粒体片段的突变体。这些突变体在FZO1基因上有缺陷,FZO1基因先前已被证明是线粒体融合所必需的。令人惊讶的是,我们发现在dnm1 fzo1双突变体中,线粒体恢复了正常形态。在dnm1 fzo1细胞中诱导Dnm1p表达会导致线粒体迅速碎片化。我们提出dnm1突变体在线粒体分裂方面存在缺陷,线粒体分裂是一种与融合相拮抗的活动。因此,我们的结果表明,线粒体形态通常由分别需要Dnm1p和Fzo1p参与的分裂和融合之间的平衡所控制。