State Key Laboratory of Virology and Modern Virology Research Center, College of Life Sciences, Wuhan University, LuoJia Hill, Wuhan 430072, China.
State Key Laboratory of Virology and Modern Virology Research Center, College of Life Sciences, Wuhan University, LuoJia Hill, Wuhan 430072, China.
Cell Host Microbe. 2017 Apr 12;21(4):538-547.e4. doi: 10.1016/j.chom.2017.03.004.
Mitophagy is a form of autophagy that selectively removes damaged mitochondria. Impaired mitochondria can be tagged by the kinase PINK1, which triggers recruitment of the E3-ubiquitin ligase Parkin and subsequent mitochondrial sequestration within autophagosomes. We previously found that human parainfluenza virus type 3 (HPIV3) infection induces autophagy, but the type and mechanisms of autophagy induction remain unknown. Here, we show that matrix protein (M) of HPIV3 translocates to mitochondria and interacts with Tu translation elongation factor mitochondrial (TUFM). M-mediated mitophagy does not require the Parkin-PINK1 pathway but rather an interaction between M and the LC3 protein that mediates autophagosome formation. These interactions with both TUFM and LC3 are required for the induction of mitophagy and lead to inhibition of the type I interferon response. These results reveal that a viral protein is sufficient to induce mitophagy by bridging autophagosomes and mitochondria.
线粒体自噬是一种选择性清除受损线粒体的自噬形式。受损的线粒体可以被激酶 PINK1 标记,这会触发 E3 泛素连接酶 Parkin 的募集,随后线粒体被隔离在自噬体中。我们之前发现,人类副流感病毒 3 型(HPIV3)感染会诱导自噬,但自噬的类型和机制尚不清楚。在这里,我们表明,HPIV3 的基质蛋白(M)易位到线粒体,并与 Tu 翻译延伸因子线粒体(TUFM)相互作用。M 介导的线粒体自噬不需要 Parkin-PINK1 途径,而是需要 M 与 LC3 蛋白之间的相互作用,后者介导自噬体的形成。与 TUFM 和 LC3 的这些相互作用对于诱导线粒体自噬是必需的,并导致 I 型干扰素反应的抑制。这些结果表明,一种病毒蛋白通过桥接自噬体和线粒体,足以诱导线粒体自噬。