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Mitochondrial DNA replication: a PrimPol perspective

PrimPol, (primase–polymerase), the most recently identified eukaryotic polymerase, has roles in both nuclear and mitochondrial DNA maintenance. PrimPol is capable of acting as a DNA polymerase, with the ability to extend primers and also bypass a variety of oxidative and photolesions. In addition, P...

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Autores principales: Bailey, Laura J., Doherty, Aidan J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5390496/
https://www.ncbi.nlm.nih.gov/pubmed/28408491
http://dx.doi.org/10.1042/BST20160162
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author Bailey, Laura J.
Doherty, Aidan J.
author_facet Bailey, Laura J.
Doherty, Aidan J.
author_sort Bailey, Laura J.
collection PubMed
description PrimPol, (primase–polymerase), the most recently identified eukaryotic polymerase, has roles in both nuclear and mitochondrial DNA maintenance. PrimPol is capable of acting as a DNA polymerase, with the ability to extend primers and also bypass a variety of oxidative and photolesions. In addition, PrimPol also functions as a primase, catalysing the preferential formation of DNA primers in a zinc finger-dependent manner. Although PrimPol's catalytic activities have been uncovered in vitro, we still know little about how and why it is targeted to the mitochondrion and what its key roles are in the maintenance of this multicopy DNA molecule. Unlike nuclear DNA, the mammalian mitochondrial genome is circular and the organelle has many unique proteins essential for its maintenance, presenting a differing environment within which PrimPol must function. Here, we discuss what is currently known about the mechanisms of DNA replication in the mitochondrion, the proteins that carry out these processes and how PrimPol is likely to be involved in assisting this vital cellular process.
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spelling pubmed-53904962017-05-01 Mitochondrial DNA replication: a PrimPol perspective Bailey, Laura J. Doherty, Aidan J. Biochem Soc Trans Review Articles PrimPol, (primase–polymerase), the most recently identified eukaryotic polymerase, has roles in both nuclear and mitochondrial DNA maintenance. PrimPol is capable of acting as a DNA polymerase, with the ability to extend primers and also bypass a variety of oxidative and photolesions. In addition, PrimPol also functions as a primase, catalysing the preferential formation of DNA primers in a zinc finger-dependent manner. Although PrimPol's catalytic activities have been uncovered in vitro, we still know little about how and why it is targeted to the mitochondrion and what its key roles are in the maintenance of this multicopy DNA molecule. Unlike nuclear DNA, the mammalian mitochondrial genome is circular and the organelle has many unique proteins essential for its maintenance, presenting a differing environment within which PrimPol must function. Here, we discuss what is currently known about the mechanisms of DNA replication in the mitochondrion, the proteins that carry out these processes and how PrimPol is likely to be involved in assisting this vital cellular process. Portland Press Ltd. 2017-04-15 2017-04-13 /pmc/articles/PMC5390496/ /pubmed/28408491 http://dx.doi.org/10.1042/BST20160162 Text en © 2017 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0) .
spellingShingle Review Articles
Bailey, Laura J.
Doherty, Aidan J.
Mitochondrial DNA replication: a PrimPol perspective
title Mitochondrial DNA replication: a PrimPol perspective
title_full Mitochondrial DNA replication: a PrimPol perspective
title_fullStr Mitochondrial DNA replication: a PrimPol perspective
title_full_unstemmed Mitochondrial DNA replication: a PrimPol perspective
title_short Mitochondrial DNA replication: a PrimPol perspective
title_sort mitochondrial dna replication: a primpol perspective
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5390496/
https://www.ncbi.nlm.nih.gov/pubmed/28408491
http://dx.doi.org/10.1042/BST20160162
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