Department of Cell and Developmental Biology, School of Medicine, Tel Aviv University, Tel Aviv, 69978, Israel.
Faculty of Biology, Ludwig-Maximilians-University Munich, Munich, Germany.
Free Radic Biol Med. 2024 Mar;214:19-27. doi: 10.1016/j.freeradbiomed.2024.01.050. Epub 2024 Jan 30.
Mitochondria are the powerhouses of cells, responsible for energy production and regulation of cellular homeostasis. When mitochondrial function is impaired, a stress response termed mitochondrial unfolded protein response (UPRmt) is initiated to restore mitochondrial function. Since mitochondria and UPRmt are implicated in many diseases, it is important to understand UPRmt regulation. In this study, we show that the SUMO protease ULP-2 has a key role in regulating mitochondrial function and UPRmt. Specifically, down-regulation of ulp-2 suppresses UPRmt and reduces mitochondrial membrane potential without significantly affecting cellular ROS. Mitochondrial networks are expanded in ulp-2 null mutants with larger mitochondrial area and increased branching. Moreover, the amount of mitochondrial DNA is increased in ulp-2 mutants. Downregulation of ULP-2 also leads to alterations in expression levels of mitochondrial genes involved in protein import and mtDNA replication, however, mitophagy remains unaltered. In summary, this study demonstrates that ULP-2 is required for mitochondrial homeostasis and the UPRmt.
线粒体是细胞的能量工厂,负责能量产生和细胞内稳态的调节。当线粒体功能受损时,会启动一种称为线粒体未折叠蛋白反应 (UPRmt) 的应激反应来恢复线粒体功能。由于线粒体和 UPRmt 与许多疾病有关,因此了解 UPRmt 的调节机制非常重要。在这项研究中,我们表明 SUMO 蛋白酶 ULP-2 在调节线粒体功能和 UPRmt 中起着关键作用。具体来说,ulp-2 的下调抑制了 UPRmt 并降低了线粒体膜电位,而对细胞内 ROS 的影响不大。ulp-2 缺失突变体中线粒体网络扩张,线粒体面积增大,分支增加。此外,ulp-2 突变体中线粒体 DNA 的含量增加。下调 ULP-2 还会导致参与蛋白质导入和 mtDNA 复制的线粒体基因的表达水平发生变化,但线粒体自噬保持不变。总之,这项研究表明 ULP-2 是线粒体动态平衡和 UPRmt 所必需的。