Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Kropp, Heike M., Ludmann, Samra, Diederichs, Kay, Betz, Karin, Marx, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
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
_version_ 1784600412936994816
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
work_keys_str_mv AT kroppheikem structuralbasisfortherecognitionofdeaminatednucleobasesbyanarchaealdnapolymerase
AT ludmannsamra structuralbasisfortherecognitionofdeaminatednucleobasesbyanarchaealdnapolymerase
AT diederichskay structuralbasisfortherecognitionofdeaminatednucleobasesbyanarchaealdnapolymerase
AT betzkarin structuralbasisfortherecognitionofdeaminatednucleobasesbyanarchaealdnapolymerase
AT marxandreas structuralbasisfortherecognitionofdeaminatednucleobasesbyanarchaealdnapolymerase