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DNA polymerases ζ and Rev1 mediate error-prone bypass of non-B DNA structures

DNA polymerase ζ (Pol ζ) and Rev1 are key players in translesion DNA synthesis. The error-prone Pol ζ can also participate in replication of undamaged DNA when the normal replisome is impaired. Here we define the nature of the replication disturbances that trigger the recruitment of error-prone poly...

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Autores principales: Northam, Matthew R., Moore, Elizabeth A., Mertz, Tony M., Binz, Sara K., Stith, Carrie M., Stepchenkova, Elena I., Wendt, Kathern L., Burgers, Peter M. J., Shcherbakova, Polina V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3874155/
https://www.ncbi.nlm.nih.gov/pubmed/24049079
http://dx.doi.org/10.1093/nar/gkt830
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author Northam, Matthew R.
Moore, Elizabeth A.
Mertz, Tony M.
Binz, Sara K.
Stith, Carrie M.
Stepchenkova, Elena I.
Wendt, Kathern L.
Burgers, Peter M. J.
Shcherbakova, Polina V.
author_facet Northam, Matthew R.
Moore, Elizabeth A.
Mertz, Tony M.
Binz, Sara K.
Stith, Carrie M.
Stepchenkova, Elena I.
Wendt, Kathern L.
Burgers, Peter M. J.
Shcherbakova, Polina V.
author_sort Northam, Matthew R.
collection PubMed
description DNA polymerase ζ (Pol ζ) and Rev1 are key players in translesion DNA synthesis. The error-prone Pol ζ can also participate in replication of undamaged DNA when the normal replisome is impaired. Here we define the nature of the replication disturbances that trigger the recruitment of error-prone polymerases in the absence of DNA damage and describe the specific roles of Rev1 and Pol ζ in handling these disturbances. We show that Pol ζ/Rev1-dependent mutations occur at sites of replication stalling at short repeated sequences capable of forming hairpin structures. The Rev1 deoxycytidyl transferase can take over the stalled replicative polymerase and incorporate an additional ‘C’ at the hairpin base. Full hairpin bypass often involves template-switching DNA synthesis, subsequent realignment generating multiply mismatched primer termini and extension of these termini by Pol ζ. The postreplicative pathway dependent on polyubiquitylation of proliferating cell nuclear antigen provides a backup mechanism for accurate bypass of these sequences that is primarily used when the Pol ζ/Rev1-dependent pathway is inactive. The results emphasize the pivotal role of noncanonical DNA structures in mutagenesis and reveal the long-sought-after mechanism of complex mutations that represent a unique signature of Pol ζ.
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spelling pubmed-38741552013-12-28 DNA polymerases ζ and Rev1 mediate error-prone bypass of non-B DNA structures Northam, Matthew R. Moore, Elizabeth A. Mertz, Tony M. Binz, Sara K. Stith, Carrie M. Stepchenkova, Elena I. Wendt, Kathern L. Burgers, Peter M. J. Shcherbakova, Polina V. Nucleic Acids Res Genome Integrity, Repair and Replication DNA polymerase ζ (Pol ζ) and Rev1 are key players in translesion DNA synthesis. The error-prone Pol ζ can also participate in replication of undamaged DNA when the normal replisome is impaired. Here we define the nature of the replication disturbances that trigger the recruitment of error-prone polymerases in the absence of DNA damage and describe the specific roles of Rev1 and Pol ζ in handling these disturbances. We show that Pol ζ/Rev1-dependent mutations occur at sites of replication stalling at short repeated sequences capable of forming hairpin structures. The Rev1 deoxycytidyl transferase can take over the stalled replicative polymerase and incorporate an additional ‘C’ at the hairpin base. Full hairpin bypass often involves template-switching DNA synthesis, subsequent realignment generating multiply mismatched primer termini and extension of these termini by Pol ζ. The postreplicative pathway dependent on polyubiquitylation of proliferating cell nuclear antigen provides a backup mechanism for accurate bypass of these sequences that is primarily used when the Pol ζ/Rev1-dependent pathway is inactive. The results emphasize the pivotal role of noncanonical DNA structures in mutagenesis and reveal the long-sought-after mechanism of complex mutations that represent a unique signature of Pol ζ. Oxford University Press 2014-01-01 2013-09-18 /pmc/articles/PMC3874155/ /pubmed/24049079 http://dx.doi.org/10.1093/nar/gkt830 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Genome Integrity, Repair and Replication
Northam, Matthew R.
Moore, Elizabeth A.
Mertz, Tony M.
Binz, Sara K.
Stith, Carrie M.
Stepchenkova, Elena I.
Wendt, Kathern L.
Burgers, Peter M. J.
Shcherbakova, Polina V.
DNA polymerases ζ and Rev1 mediate error-prone bypass of non-B DNA structures
title DNA polymerases ζ and Rev1 mediate error-prone bypass of non-B DNA structures
title_full DNA polymerases ζ and Rev1 mediate error-prone bypass of non-B DNA structures
title_fullStr DNA polymerases ζ and Rev1 mediate error-prone bypass of non-B DNA structures
title_full_unstemmed DNA polymerases ζ and Rev1 mediate error-prone bypass of non-B DNA structures
title_short DNA polymerases ζ and Rev1 mediate error-prone bypass of non-B DNA structures
title_sort dna polymerases ζ and rev1 mediate error-prone bypass of non-b dna structures
topic Genome Integrity, Repair and Replication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3874155/
https://www.ncbi.nlm.nih.gov/pubmed/24049079
http://dx.doi.org/10.1093/nar/gkt830
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