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SUV3 Helicase and Mitochondrial Homeostasis

SUV3 is a nuclear-encoded helicase that is highly conserved and localizes to the mitochondrial matrix. In yeast, loss of SUV3 function leads to the accumulation of group 1 intron transcripts, ultimately resulting in the loss of mitochondrial DNA, causing a petite phenotype. However, the mechanism le...

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Autor principal: Chen, Phang-Lang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10253155/
https://www.ncbi.nlm.nih.gov/pubmed/37298184
http://dx.doi.org/10.3390/ijms24119233
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author Chen, Phang-Lang
author_facet Chen, Phang-Lang
author_sort Chen, Phang-Lang
collection PubMed
description SUV3 is a nuclear-encoded helicase that is highly conserved and localizes to the mitochondrial matrix. In yeast, loss of SUV3 function leads to the accumulation of group 1 intron transcripts, ultimately resulting in the loss of mitochondrial DNA, causing a petite phenotype. However, the mechanism leading to the loss of mitochondrial DNA remains unknown. SUV3 is essential for survival in higher eukaryotes, and its knockout in mice results in early embryonic lethality. Heterozygous mice exhibit a range of phenotypes, including premature aging and an increased cancer incidence. Furthermore, cells derived from SUV3 heterozygotes or knockdown cultural cells show a reduction in mtDNA. Transient downregulation of SUV3 leads to the formation of R-loops and the accumulation of double-stranded RNA in mitochondria. This review aims to provide an overview of the current knowledge regarding the SUV3-containing complex and discuss its potential mechanism for tumor suppression activity.
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spelling pubmed-102531552023-06-10 SUV3 Helicase and Mitochondrial Homeostasis Chen, Phang-Lang Int J Mol Sci Review SUV3 is a nuclear-encoded helicase that is highly conserved and localizes to the mitochondrial matrix. In yeast, loss of SUV3 function leads to the accumulation of group 1 intron transcripts, ultimately resulting in the loss of mitochondrial DNA, causing a petite phenotype. However, the mechanism leading to the loss of mitochondrial DNA remains unknown. SUV3 is essential for survival in higher eukaryotes, and its knockout in mice results in early embryonic lethality. Heterozygous mice exhibit a range of phenotypes, including premature aging and an increased cancer incidence. Furthermore, cells derived from SUV3 heterozygotes or knockdown cultural cells show a reduction in mtDNA. Transient downregulation of SUV3 leads to the formation of R-loops and the accumulation of double-stranded RNA in mitochondria. This review aims to provide an overview of the current knowledge regarding the SUV3-containing complex and discuss its potential mechanism for tumor suppression activity. MDPI 2023-05-25 /pmc/articles/PMC10253155/ /pubmed/37298184 http://dx.doi.org/10.3390/ijms24119233 Text en © 2023 by the author. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Chen, Phang-Lang
SUV3 Helicase and Mitochondrial Homeostasis
title SUV3 Helicase and Mitochondrial Homeostasis
title_full SUV3 Helicase and Mitochondrial Homeostasis
title_fullStr SUV3 Helicase and Mitochondrial Homeostasis
title_full_unstemmed SUV3 Helicase and Mitochondrial Homeostasis
title_short SUV3 Helicase and Mitochondrial Homeostasis
title_sort suv3 helicase and mitochondrial homeostasis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10253155/
https://www.ncbi.nlm.nih.gov/pubmed/37298184
http://dx.doi.org/10.3390/ijms24119233
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