Gatti Priya, Schiavon Cara, Cicero Julien, Manor Uri, Germain Marc
Groupe de Recherche en Signalisation Cellulaire and Département de Biologie Médicale, Université du Québec à Trois-Rivières, Trois-Rivières, QC, Canada.
Centre d'Excellence en Recherche sur les Maladies Orphelines - Fondation Courtois, Université du Québec à Montréal, Montréal, QC, Canada.
Nat Commun. 2025 Jan 7;16(1):451. doi: 10.1038/s41467-024-55758-x.
Mitochondria are crucial for cellular metabolism and signalling. Mitochondrial activity is modulated by mitochondrial fission and fusion, which are required to properly balance metabolic functions, transfer material between mitochondria, and remove defective mitochondria. Mitochondrial fission occurs at mitochondria-endoplasmic reticulum (ER) contact sites, and requires the formation of actin filaments that drive mitochondrial constriction and the recruitment of the fission protein DRP1. The role of actin in mitochondrial fusion remains entirely unexplored. Here we show that preventing actin polymerisation on either mitochondria or the ER disrupts both fission and fusion. We show that fusion but not fission is dependent on Arp2/3, whereas both fission and fusion require INF2 formin-dependent actin polymerization. We also show that mitochondria-associated actin marks fusion sites prior to the fusion protein MFN2. Together, our work introduces a method for perturbing organelle-associated actin and demonstrates a previously unknown role for actin in mitochondrial fusion.
线粒体对于细胞代谢和信号传导至关重要。线粒体活性受线粒体分裂和融合调节,这对于适当平衡代谢功能、在线粒体之间转移物质以及清除有缺陷的线粒体是必需的。线粒体分裂发生在线粒体-内质网(ER)接触位点,需要形成驱动线粒体收缩的肌动蛋白丝并募集分裂蛋白DRP1。肌动蛋白在线粒体融合中的作用仍完全未被探索。在这里,我们表明阻止肌动蛋白在线粒体或内质网上聚合会破坏分裂和融合。我们表明融合而非分裂依赖于Arp2/3,而分裂和融合都需要INF2formin依赖的肌动蛋白聚合。我们还表明,与线粒体相关的肌动蛋白在融合蛋白MFN2之前标记融合位点。总之,我们的工作引入了一种干扰细胞器相关肌动蛋白的方法,并证明了肌动蛋白在线粒体融合中以前未知的作用。