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The Roles of UmuD in Regulating Mutagenesis

All organisms are subject to DNA damage from both endogenous and environmental sources. DNA damage that is not fully repaired can lead to mutations. Mutagenesis is now understood to be an active process, in part facilitated by lower-fidelity DNA polymerases that replicate DNA in an error-prone manne...

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Detalles Bibliográficos
Autores principales: Ollivierre, Jaylene N., Fang, Jing, Beuning, Penny J.
Formato: Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2948943/
https://www.ncbi.nlm.nih.gov/pubmed/20936072
http://dx.doi.org/10.4061/2010/947680
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author Ollivierre, Jaylene N.
Fang, Jing
Beuning, Penny J.
author_facet Ollivierre, Jaylene N.
Fang, Jing
Beuning, Penny J.
author_sort Ollivierre, Jaylene N.
collection PubMed
description All organisms are subject to DNA damage from both endogenous and environmental sources. DNA damage that is not fully repaired can lead to mutations. Mutagenesis is now understood to be an active process, in part facilitated by lower-fidelity DNA polymerases that replicate DNA in an error-prone manner. Y-family DNA polymerases, found throughout all domains of life, are characterized by their lower fidelity on undamaged DNA and their specialized ability to copy damaged DNA. Two E. coli Y-family DNA polymerases are responsible for copying damaged DNA as well as for mutagenesis. These DNA polymerases interact with different forms of UmuD, a dynamic protein that regulates mutagenesis. The UmuD gene products, regulated by the SOS response, exist in two principal forms: UmuD(2), which prevents mutagenesis, and UmuD(2)′, which facilitates UV-induced mutagenesis. This paper focuses on the multiple conformations of the UmuD gene products and how their protein interactions regulate mutagenesis.
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spelling pubmed-29489432010-10-08 The Roles of UmuD in Regulating Mutagenesis Ollivierre, Jaylene N. Fang, Jing Beuning, Penny J. J Nucleic Acids Review Article All organisms are subject to DNA damage from both endogenous and environmental sources. DNA damage that is not fully repaired can lead to mutations. Mutagenesis is now understood to be an active process, in part facilitated by lower-fidelity DNA polymerases that replicate DNA in an error-prone manner. Y-family DNA polymerases, found throughout all domains of life, are characterized by their lower fidelity on undamaged DNA and their specialized ability to copy damaged DNA. Two E. coli Y-family DNA polymerases are responsible for copying damaged DNA as well as for mutagenesis. These DNA polymerases interact with different forms of UmuD, a dynamic protein that regulates mutagenesis. The UmuD gene products, regulated by the SOS response, exist in two principal forms: UmuD(2), which prevents mutagenesis, and UmuD(2)′, which facilitates UV-induced mutagenesis. This paper focuses on the multiple conformations of the UmuD gene products and how their protein interactions regulate mutagenesis. SAGE-Hindawi Access to Research 2010-09-30 /pmc/articles/PMC2948943/ /pubmed/20936072 http://dx.doi.org/10.4061/2010/947680 Text en Copyright © 2010 Jaylene N. Ollivierre et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Ollivierre, Jaylene N.
Fang, Jing
Beuning, Penny J.
The Roles of UmuD in Regulating Mutagenesis
title The Roles of UmuD in Regulating Mutagenesis
title_full The Roles of UmuD in Regulating Mutagenesis
title_fullStr The Roles of UmuD in Regulating Mutagenesis
title_full_unstemmed The Roles of UmuD in Regulating Mutagenesis
title_short The Roles of UmuD in Regulating Mutagenesis
title_sort roles of umud in regulating mutagenesis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2948943/
https://www.ncbi.nlm.nih.gov/pubmed/20936072
http://dx.doi.org/10.4061/2010/947680
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