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PrimPol, an Archaic Primase/Polymerase Operating in Human Cells
We describe a second primase in human cells, PrimPol, which has the ability to start DNA chains with deoxynucleotides unlike regular primases, which use exclusively ribonucleotides. Moreover, PrimPol is also a DNA polymerase tailored to bypass the most common oxidative lesions in DNA, such as abasic...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3899013/ https://www.ncbi.nlm.nih.gov/pubmed/24207056 http://dx.doi.org/10.1016/j.molcel.2013.09.025 |
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author | García-Gómez, Sara Reyes, Aurelio Martínez-Jiménez, María I. Chocrón, E. Sandra Mourón, Silvana Terrados, Gloria Powell, Christopher Salido, Eduardo Méndez, Juan Holt, Ian J. Blanco, Luis |
author_facet | García-Gómez, Sara Reyes, Aurelio Martínez-Jiménez, María I. Chocrón, E. Sandra Mourón, Silvana Terrados, Gloria Powell, Christopher Salido, Eduardo Méndez, Juan Holt, Ian J. Blanco, Luis |
author_sort | García-Gómez, Sara |
collection | PubMed |
description | We describe a second primase in human cells, PrimPol, which has the ability to start DNA chains with deoxynucleotides unlike regular primases, which use exclusively ribonucleotides. Moreover, PrimPol is also a DNA polymerase tailored to bypass the most common oxidative lesions in DNA, such as abasic sites and 8-oxoguanine. Subcellular fractionation and immunodetection studies indicated that PrimPol is present in both nuclear and mitochondrial DNA compartments. PrimPol activity is detectable in mitochondrial lysates from human and mouse cells but is absent from mitochondria derived from PRIMPOL knockout mice. PRIMPOL gene silencing or ablation in human and mouse cells impaired mitochondrial DNA replication. On the basis of the synergy observed with replicative DNA polymerases Polγ and Polε, PrimPol is proposed to facilitate replication fork progression by acting as a translesion DNA polymerase or as a specific DNA primase reinitiating downstream of lesions that block synthesis during both mitochondrial and nuclear DNA replication. |
format | Online Article Text |
id | pubmed-3899013 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-38990132014-01-24 PrimPol, an Archaic Primase/Polymerase Operating in Human Cells García-Gómez, Sara Reyes, Aurelio Martínez-Jiménez, María I. Chocrón, E. Sandra Mourón, Silvana Terrados, Gloria Powell, Christopher Salido, Eduardo Méndez, Juan Holt, Ian J. Blanco, Luis Mol Cell Article We describe a second primase in human cells, PrimPol, which has the ability to start DNA chains with deoxynucleotides unlike regular primases, which use exclusively ribonucleotides. Moreover, PrimPol is also a DNA polymerase tailored to bypass the most common oxidative lesions in DNA, such as abasic sites and 8-oxoguanine. Subcellular fractionation and immunodetection studies indicated that PrimPol is present in both nuclear and mitochondrial DNA compartments. PrimPol activity is detectable in mitochondrial lysates from human and mouse cells but is absent from mitochondria derived from PRIMPOL knockout mice. PRIMPOL gene silencing or ablation in human and mouse cells impaired mitochondrial DNA replication. On the basis of the synergy observed with replicative DNA polymerases Polγ and Polε, PrimPol is proposed to facilitate replication fork progression by acting as a translesion DNA polymerase or as a specific DNA primase reinitiating downstream of lesions that block synthesis during both mitochondrial and nuclear DNA replication. Cell Press 2013-11-21 /pmc/articles/PMC3899013/ /pubmed/24207056 http://dx.doi.org/10.1016/j.molcel.2013.09.025 Text en © 2013 ELL & Excerpta Medica. https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article García-Gómez, Sara Reyes, Aurelio Martínez-Jiménez, María I. Chocrón, E. Sandra Mourón, Silvana Terrados, Gloria Powell, Christopher Salido, Eduardo Méndez, Juan Holt, Ian J. Blanco, Luis PrimPol, an Archaic Primase/Polymerase Operating in Human Cells |
title | PrimPol, an Archaic Primase/Polymerase Operating in Human Cells |
title_full | PrimPol, an Archaic Primase/Polymerase Operating in Human Cells |
title_fullStr | PrimPol, an Archaic Primase/Polymerase Operating in Human Cells |
title_full_unstemmed | PrimPol, an Archaic Primase/Polymerase Operating in Human Cells |
title_short | PrimPol, an Archaic Primase/Polymerase Operating in Human Cells |
title_sort | primpol, an archaic primase/polymerase operating in human cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3899013/ https://www.ncbi.nlm.nih.gov/pubmed/24207056 http://dx.doi.org/10.1016/j.molcel.2013.09.025 |
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