MOE Key Laboratory for Cellular Dynamics & Center for Advanced Interdisciplinary Science and Biomedicine of IHM, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
Anhui Key Laboratory of Cellular Dynamics and Chemical Biology & Hefei National Research Center for Interdisciplinary Sciences at the Microscale, School of Life Sciences, University of Science and Technology of China, Hefei, China.
PLoS Biol. 2023 Aug 17;21(8):e3002247. doi: 10.1371/journal.pbio.3002247. eCollection 2023 Aug.
Mitochondria are in a constant balance of fusion and fission. Excessive fission or deficient fusion leads to mitochondrial fragmentation, causing mitochondrial dysfunction and physiological disorders. How the cell prevents excessive fission of mitochondria is not well understood. Here, we report that the fission yeast AAA-ATPase Yta4, which is the homolog of budding yeast Msp1 responsible for clearing mistargeted tail-anchored (TA) proteins on mitochondria, plays a critical role in preventing excessive mitochondrial fission. The absence of Yta4 leads to mild mitochondrial fragmentation in a Dnm1-dependent manner but severe mitochondrial fragmentation upon induction of mitochondrial depolarization. Overexpression of Yta4 delocalizes the receptor proteins of Dnm1, i.e., Fis1 (a TA protein) and Mdv1 (the bridging protein between Fis1 and Dnm1), from mitochondria and reduces the localization of Dnm1 to mitochondria. The effect of Yta4 overexpression on Fis1 and Mdv1, but not Dnm1, depends on the ATPase and translocase activities of Yta4. Moreover, Yta4 interacts with Dnm1, Mdv1, and Fis1. In addition, Yta4 competes with Dnm1 for binding Mdv1 and decreases the affinity of Dnm1 for GTP and inhibits Dnm1 assembly in vitro. These findings suggest a model, in which Yta4 inhibits mitochondrial fission by inhibiting the function of the mitochondrial divisome composed of Fis1, Mdv1, and Dnm1. Therefore, the present work reveals an uncharacterized molecular mechanism underlying the inhibition of mitochondrial fission.
线粒体处于融合和裂变的不断平衡中。过度的裂变或融合不足会导致线粒体碎片化,从而导致线粒体功能障碍和生理紊乱。细胞如何防止线粒体过度裂变还不是很清楚。在这里,我们报告说,裂殖酵母 AAA-ATPase Yta4,它是芽殖酵母 Msp1 的同源物,负责清除线粒体上靶向错误的尾巴锚定(TA)蛋白,在防止线粒体过度裂变中起着关键作用。Yta4 的缺失以 Dnm1 依赖的方式导致轻度的线粒体碎片化,但在诱导线粒体去极化时会导致严重的线粒体碎片化。Yta4 的过表达使 Dnm1 的受体蛋白,即 Fis1(TA 蛋白)和 Mdv1(Fis1 和 Dnm1 之间的桥接蛋白),从线粒体中解聚,并减少 Dnm1 在线粒体中的定位。Yta4 过表达对 Fis1 和 Mdv1 的影响,但不是 Dnm1,取决于 Yta4 的 ATPase 和易位酶活性。此外,Yta4 与 Dnm1、Mdv1 和 Fis1 相互作用。此外,Yta4 与 Dnm1 竞争结合 Mdv1,并降低 Dnm1 对 GTP 的亲和力,体外抑制 Dnm1 组装。这些发现提出了一个模型,即 Yta4 通过抑制由 Fis1、Mdv1 和 Dnm1 组成的线粒体分裂体的功能来抑制线粒体裂变。因此,本工作揭示了一种抑制线粒体裂变的未表征的分子机制。