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Translesion DNA synthesis in the context of cancer research

During cell division, replication of the genomic DNA is performed by high-fidelity DNA polymerases but these error-free enzymes can not synthesize across damaged DNA. Specialized DNA polymerases, so called DNA translesion synthesis polymerases (TLS polymerases), can replicate damaged DNA thereby avo...

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Detalles Bibliográficos
Autores principales: Knobel, Philip A, Marti, Thomas M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3224763/
https://www.ncbi.nlm.nih.gov/pubmed/22047021
http://dx.doi.org/10.1186/1475-2867-11-39
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author Knobel, Philip A
Marti, Thomas M
author_facet Knobel, Philip A
Marti, Thomas M
author_sort Knobel, Philip A
collection PubMed
description During cell division, replication of the genomic DNA is performed by high-fidelity DNA polymerases but these error-free enzymes can not synthesize across damaged DNA. Specialized DNA polymerases, so called DNA translesion synthesis polymerases (TLS polymerases), can replicate damaged DNA thereby avoiding replication fork breakdown and subsequent chromosomal instability. We focus on the involvement of mammalian TLS polymerases in DNA damage tolerance mechanisms. In detail, we review the discovery of TLS polymerases and describe the molecular features of all the mammalian TLS polymerases identified so far. We give a short overview of the mechanisms that regulate the selectivity and activity of TLS polymerases. In addition, we summarize the current knowledge how different types of DNA damage, relevant either for the induction or treatment of cancer, are bypassed by TLS polymerases. Finally, we elucidate the relevance of TLS polymerases in the context of cancer therapy.
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spelling pubmed-32247632011-11-28 Translesion DNA synthesis in the context of cancer research Knobel, Philip A Marti, Thomas M Cancer Cell Int Review During cell division, replication of the genomic DNA is performed by high-fidelity DNA polymerases but these error-free enzymes can not synthesize across damaged DNA. Specialized DNA polymerases, so called DNA translesion synthesis polymerases (TLS polymerases), can replicate damaged DNA thereby avoiding replication fork breakdown and subsequent chromosomal instability. We focus on the involvement of mammalian TLS polymerases in DNA damage tolerance mechanisms. In detail, we review the discovery of TLS polymerases and describe the molecular features of all the mammalian TLS polymerases identified so far. We give a short overview of the mechanisms that regulate the selectivity and activity of TLS polymerases. In addition, we summarize the current knowledge how different types of DNA damage, relevant either for the induction or treatment of cancer, are bypassed by TLS polymerases. Finally, we elucidate the relevance of TLS polymerases in the context of cancer therapy. BioMed Central 2011-11-02 /pmc/articles/PMC3224763/ /pubmed/22047021 http://dx.doi.org/10.1186/1475-2867-11-39 Text en Copyright ©2011 Knobel and Marti; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Knobel, Philip A
Marti, Thomas M
Translesion DNA synthesis in the context of cancer research
title Translesion DNA synthesis in the context of cancer research
title_full Translesion DNA synthesis in the context of cancer research
title_fullStr Translesion DNA synthesis in the context of cancer research
title_full_unstemmed Translesion DNA synthesis in the context of cancer research
title_short Translesion DNA synthesis in the context of cancer research
title_sort translesion dna synthesis in the context of cancer research
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3224763/
https://www.ncbi.nlm.nih.gov/pubmed/22047021
http://dx.doi.org/10.1186/1475-2867-11-39
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