ULP-2 SUMO protease regulates UPRmt and mitochondrial homeostasis in Caenorhabditis elegans

被引:4
|
作者
Michaeli, Lirin [1 ]
Spector, Eyal [1 ]
Haeussler, Simon [2 ]
Carvalho, Catia A. [1 ]
Grobe, Hanna [1 ]
Abu-Shach, Ulrike Bening [1 ]
Zinger, Hen [1 ]
Conradt, Barbara [2 ,3 ]
Broday, Limor [1 ]
机构
[1] Tel Aviv Univ, Sch Med, Dept Cell & Dev Biol, IL-69978 Tel Aviv, Israel
[2] Ludwig Maximilians Univ Munchen, Fac Biol, Munich, Germany
[3] UCL, Dept Cell & Dev Biol, Div Biosci, London, England
基金
以色列科学基金会;
关键词
SUMO; Smo-1; ULP-2; SUMO protease; SENP; Mitochondrial unfolded protein response; UPRmt; NUCLEAR RESPIRATORY FACTORS; TRANSCRIPTION FACTOR; GENE-EXPRESSION; SUMOYLATION; IMPORT; MITOPHAGY; PLATFORM; FISSION;
D O I
10.1016/j.freeradbiomed.2024.01.050
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:19 / 27
页数:9
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