4.5 Review

Mitochondrial E3 ubiquitin ligase 1 (MUL1) as a novel therapeutic target for diseases associated with mitochondrial dysfunction

期刊

IUBMB LIFE
卷 74, 期 9, 页码 850-865

出版社

WILEY
DOI: 10.1002/iub.2657

关键词

Akt; and RNF218; C1orf166; cell death; FLJ12875; GIDE; inflammation; MAPL; mitochondria morphology; mitochondrial E3 ubiquitin ligase 1; MULAN

资金

  1. Agencia Nacional de Investigacion y Desarrollo (ANID), Chile [FONDECYT 1211731, FONDECYT 1200490, FONDECYT1190743, FONDAP15130011]
  2. U-Redes Generacion, Vicerrectoria de Investigacion y Desarrollo, Universidad de Chile [URG-035/1]
  3. CRP-ICGEB [CHL18-04]

向作者/读者索取更多资源

MUL1 is a protein involved in various cellular processes, including mitochondrial dynamics, cell survival, and tumor suppression. It plays a role in inflammatory response, cancer, neurological diseases, and cardiovascular diseases. This review summarizes the functions of MUL1 in different pathological models and discusses its potential as a therapeutic target.
Mitochondrial E3 ubiquitin ligase 1 (MUL1) is a mitochondrial outer membrane-anchored protein-containing transmembrane domain in its N- and C-terminal regions, where both are exposed to the cytosol. Interestingly the C-terminal region has a RING finger domain responsible for its E3 ligase activity, as ubiquitin or in SUMOylation, interacting with proteins related to mitochondrial fusion and fission, cell survival, and tumor suppressor process, such as Akt. Therefore, MUL1 is involved in various cellular processes, such as mitochondrial dynamics, inter-organelle communication, proliferation, mitophagy, immune response, inflammation and cell apoptosis. MUL1 is expressed at a higher basal level in the heart, immune system organs, and blood. Here, we discuss the role of MUL1 in mitochondrial dynamics and its function in various pathological models, both in vitro and in vivo. In this context, we describe the role of MUL1 in: (1) the inflammatory response, by regulating NF-kappa B activity; (2) cancer, by promoting cell death and regulating exonuclear function of proteins, such as p53; (3) neurological diseases, by maintaining communication with other organelles and interacting with proteins to eliminate damaged organelles and; (4) cardiovascular diseases, by maintaining mitochondrial fusion/fission homeostasis. In this review, we summarize the latest advances in the physiological and pathological functions of MUL1. We also describe the different substrates of MUL1, acting as a positive or negative regulator in various pathologies associated with mitochondrial dysfunction. In conclusion, MUL1 could be a potential key target for the development of therapies that focus on ensuring the functionality of the mitochondrial network and, furthermore, the quality control of intracellular components by synchronously modulating the activity of different cellular mechanisms involved in the aforementioned pathologies. This, in turn, will guide the development of targeted therapies.

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