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Structural Basis for The Recognition of Deaminated Nucleobases by An Archaeal DNA Polymerase
With increasing temperature, nucleobases in DNA become increasingly damaged by hydrolysis of exocyclic amines. The most prominent damage includes the conversion of cytosine to uracil and adenine to hypoxanthine. These damages are mutagenic and put the integrity of the genome at risk if not repaired...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596578/ https://www.ncbi.nlm.nih.gov/pubmed/34486208 http://dx.doi.org/10.1002/cbic.202100306 |
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author | Kropp, Heike M. Ludmann, Samra Diederichs, Kay Betz, Karin Marx, Andreas |
author_facet | Kropp, Heike M. Ludmann, Samra Diederichs, Kay Betz, Karin Marx, Andreas |
author_sort | Kropp, Heike M. |
collection | PubMed |
description | With increasing temperature, nucleobases in DNA become increasingly damaged by hydrolysis of exocyclic amines. The most prominent damage includes the conversion of cytosine to uracil and adenine to hypoxanthine. These damages are mutagenic and put the integrity of the genome at risk if not repaired appropriately. Several archaea live at elevated temperatures and thus, are exposed to a higher risk of deamination. Earlier studies have shown that DNA polymerases of archaea have the property of sensing deaminated nucleobases in the DNA template and thereby stalling the DNA synthesis during DNA replication providing another layer of DNA damage recognition and repair. However, the structural basis of uracil and hypoxanthine sensing by archaeal B‐family DNA polymerases is sparse. Here we report on three new crystal structures of the archaeal B‐family DNA polymerase from Thermococcus kodakarensis (KOD) DNA polymerase in complex with primer and template strands that have extended single stranded DNA template 5’‐overhangs. These overhangs contain either the canonical nucleobases as well as uracil or hypoxanthine, respectively, and provide unprecedented structural insights into their recognition by archaeal B‐family DNA polymerases. |
format | Online Article Text |
id | pubmed-8596578 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85965782021-11-22 Structural Basis for The Recognition of Deaminated Nucleobases by An Archaeal DNA Polymerase Kropp, Heike M. Ludmann, Samra Diederichs, Kay Betz, Karin Marx, Andreas Chembiochem Full Papers With increasing temperature, nucleobases in DNA become increasingly damaged by hydrolysis of exocyclic amines. The most prominent damage includes the conversion of cytosine to uracil and adenine to hypoxanthine. These damages are mutagenic and put the integrity of the genome at risk if not repaired appropriately. Several archaea live at elevated temperatures and thus, are exposed to a higher risk of deamination. Earlier studies have shown that DNA polymerases of archaea have the property of sensing deaminated nucleobases in the DNA template and thereby stalling the DNA synthesis during DNA replication providing another layer of DNA damage recognition and repair. However, the structural basis of uracil and hypoxanthine sensing by archaeal B‐family DNA polymerases is sparse. Here we report on three new crystal structures of the archaeal B‐family DNA polymerase from Thermococcus kodakarensis (KOD) DNA polymerase in complex with primer and template strands that have extended single stranded DNA template 5’‐overhangs. These overhangs contain either the canonical nucleobases as well as uracil or hypoxanthine, respectively, and provide unprecedented structural insights into their recognition by archaeal B‐family DNA polymerases. John Wiley and Sons Inc. 2021-09-14 2021-11-03 /pmc/articles/PMC8596578/ /pubmed/34486208 http://dx.doi.org/10.1002/cbic.202100306 Text en © 2021 The Authors. ChemBioChem published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Kropp, Heike M. Ludmann, Samra Diederichs, Kay Betz, Karin Marx, Andreas Structural Basis for The Recognition of Deaminated Nucleobases by An Archaeal DNA Polymerase |
title | Structural Basis for The Recognition of Deaminated Nucleobases by An Archaeal DNA Polymerase |
title_full | Structural Basis for The Recognition of Deaminated Nucleobases by An Archaeal DNA Polymerase |
title_fullStr | Structural Basis for The Recognition of Deaminated Nucleobases by An Archaeal DNA Polymerase |
title_full_unstemmed | Structural Basis for The Recognition of Deaminated Nucleobases by An Archaeal DNA Polymerase |
title_short | Structural Basis for The Recognition of Deaminated Nucleobases by An Archaeal DNA Polymerase |
title_sort | structural basis for the recognition of deaminated nucleobases by an archaeal dna polymerase |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596578/ https://www.ncbi.nlm.nih.gov/pubmed/34486208 http://dx.doi.org/10.1002/cbic.202100306 |
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