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Dynamics of Mismatch and Alternative Excision-Dependent Repair in Replicating Bacillus subtilis DNA Examined Under Conditions of Neutral Selection
Spontaneous DNA deamination is a potential source of transition mutations. In Bacillus subtilis, EndoV, a component of the alternative excision repair pathway (AER), counteracts the mutagenicity of base deamination-induced mispairs. Here, we report that the mismatch repair (MMR) system, MutSL, preve...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9280176/ https://www.ncbi.nlm.nih.gov/pubmed/35847079 http://dx.doi.org/10.3389/fmicb.2022.866089 |
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author | Patlán-Vázquez, Adriana G. Ayala-García, Víctor M. Vallin, Carmen Cortés, Jonathan Vásquez-Morales, Suria G. Robleto, Eduardo A. Nudler, Evgeny Pedraza-Reyes, Mario |
author_facet | Patlán-Vázquez, Adriana G. Ayala-García, Víctor M. Vallin, Carmen Cortés, Jonathan Vásquez-Morales, Suria G. Robleto, Eduardo A. Nudler, Evgeny Pedraza-Reyes, Mario |
author_sort | Patlán-Vázquez, Adriana G. |
collection | PubMed |
description | Spontaneous DNA deamination is a potential source of transition mutations. In Bacillus subtilis, EndoV, a component of the alternative excision repair pathway (AER), counteracts the mutagenicity of base deamination-induced mispairs. Here, we report that the mismatch repair (MMR) system, MutSL, prevents the harmful effects of HNO(2), a deaminating agent of Cytosine (C), Adenine (A), and Guanine (G). Using Maximum Depth Sequencing (MDS), which measures mutagenesis under conditions of neutral selection, in B. subtilis strains proficient or deficient in MutSL and/or EndoV, revealed asymmetric and heterogeneous patterns of mutations in both DNA template strands. While the lagging template strand showed a higher frequency of C → T substitutions; G → A mutations, occurred more frequently in the leading template strand in different genetic backgrounds. In summary, our results unveiled a role for MutSL in preventing the deleterious effects of base deamination and uncovered differential patterns of base deamination processing by the AER and MMR systems that are influenced by the sequence context and the replicating DNA strand. |
format | Online Article Text |
id | pubmed-9280176 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92801762022-07-15 Dynamics of Mismatch and Alternative Excision-Dependent Repair in Replicating Bacillus subtilis DNA Examined Under Conditions of Neutral Selection Patlán-Vázquez, Adriana G. Ayala-García, Víctor M. Vallin, Carmen Cortés, Jonathan Vásquez-Morales, Suria G. Robleto, Eduardo A. Nudler, Evgeny Pedraza-Reyes, Mario Front Microbiol Microbiology Spontaneous DNA deamination is a potential source of transition mutations. In Bacillus subtilis, EndoV, a component of the alternative excision repair pathway (AER), counteracts the mutagenicity of base deamination-induced mispairs. Here, we report that the mismatch repair (MMR) system, MutSL, prevents the harmful effects of HNO(2), a deaminating agent of Cytosine (C), Adenine (A), and Guanine (G). Using Maximum Depth Sequencing (MDS), which measures mutagenesis under conditions of neutral selection, in B. subtilis strains proficient or deficient in MutSL and/or EndoV, revealed asymmetric and heterogeneous patterns of mutations in both DNA template strands. While the lagging template strand showed a higher frequency of C → T substitutions; G → A mutations, occurred more frequently in the leading template strand in different genetic backgrounds. In summary, our results unveiled a role for MutSL in preventing the deleterious effects of base deamination and uncovered differential patterns of base deamination processing by the AER and MMR systems that are influenced by the sequence context and the replicating DNA strand. Frontiers Media S.A. 2022-06-30 /pmc/articles/PMC9280176/ /pubmed/35847079 http://dx.doi.org/10.3389/fmicb.2022.866089 Text en Copyright © 2022 Patlán-Vázquez, Ayala-García, Vallin, Cortés, Vásquez-Morales, Robleto, Nudler and Pedraza-Reyes. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Patlán-Vázquez, Adriana G. Ayala-García, Víctor M. Vallin, Carmen Cortés, Jonathan Vásquez-Morales, Suria G. Robleto, Eduardo A. Nudler, Evgeny Pedraza-Reyes, Mario Dynamics of Mismatch and Alternative Excision-Dependent Repair in Replicating Bacillus subtilis DNA Examined Under Conditions of Neutral Selection |
title | Dynamics of Mismatch and Alternative Excision-Dependent Repair in Replicating Bacillus subtilis DNA Examined Under Conditions of Neutral Selection |
title_full | Dynamics of Mismatch and Alternative Excision-Dependent Repair in Replicating Bacillus subtilis DNA Examined Under Conditions of Neutral Selection |
title_fullStr | Dynamics of Mismatch and Alternative Excision-Dependent Repair in Replicating Bacillus subtilis DNA Examined Under Conditions of Neutral Selection |
title_full_unstemmed | Dynamics of Mismatch and Alternative Excision-Dependent Repair in Replicating Bacillus subtilis DNA Examined Under Conditions of Neutral Selection |
title_short | Dynamics of Mismatch and Alternative Excision-Dependent Repair in Replicating Bacillus subtilis DNA Examined Under Conditions of Neutral Selection |
title_sort | dynamics of mismatch and alternative excision-dependent repair in replicating bacillus subtilis dna examined under conditions of neutral selection |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9280176/ https://www.ncbi.nlm.nih.gov/pubmed/35847079 http://dx.doi.org/10.3389/fmicb.2022.866089 |
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