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Migrating bubble synthesis promotes mutagenesis through lesions in its template
Break-induced replication (BIR) proceeds via a migrating D-loop for hundreds of kilobases and is highly mutagenic. Previous studies identified long single-stranded (ss) nascent DNA that accumulates during leading strand synthesis to be a target for DNA damage and a primary source of BIR-induced muta...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9262586/ https://www.ncbi.nlm.nih.gov/pubmed/35748867 http://dx.doi.org/10.1093/nar/gkac520 |
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author | Osia, Beth Twarowski, Jerzy Jackson, Tyler Lobachev, Kirill Liu, Liping Malkova, Anna |
author_facet | Osia, Beth Twarowski, Jerzy Jackson, Tyler Lobachev, Kirill Liu, Liping Malkova, Anna |
author_sort | Osia, Beth |
collection | PubMed |
description | Break-induced replication (BIR) proceeds via a migrating D-loop for hundreds of kilobases and is highly mutagenic. Previous studies identified long single-stranded (ss) nascent DNA that accumulates during leading strand synthesis to be a target for DNA damage and a primary source of BIR-induced mutagenesis. Here, we describe a new important source of mutagenic ssDNA formed during BIR: the ssDNA template for leading strand BIR synthesis formed during D-loop migration. Specifically, we demonstrate that this D-loop bottom template strand (D-BTS) is susceptible to APOBEC3A (A3A)-induced DNA lesions leading to mutations associated with BIR. Also, we demonstrate that BIR-associated ssDNA promotes an additional type of genetic instability: replication slippage between microhomologies stimulated by inverted DNA repeats. Based on our results we propose that these events are stimulated by both known sources of ssDNA formed during BIR, nascent DNA formed by leading strand synthesis, and the D-BTS that we describe here. Together we report a new source of mutagenesis during BIR that may also be shared by other homologous recombination pathways driven by D-loop repair synthesis. |
format | Online Article Text |
id | pubmed-9262586 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-92625862022-07-08 Migrating bubble synthesis promotes mutagenesis through lesions in its template Osia, Beth Twarowski, Jerzy Jackson, Tyler Lobachev, Kirill Liu, Liping Malkova, Anna Nucleic Acids Res Genome Integrity, Repair and Replication Break-induced replication (BIR) proceeds via a migrating D-loop for hundreds of kilobases and is highly mutagenic. Previous studies identified long single-stranded (ss) nascent DNA that accumulates during leading strand synthesis to be a target for DNA damage and a primary source of BIR-induced mutagenesis. Here, we describe a new important source of mutagenic ssDNA formed during BIR: the ssDNA template for leading strand BIR synthesis formed during D-loop migration. Specifically, we demonstrate that this D-loop bottom template strand (D-BTS) is susceptible to APOBEC3A (A3A)-induced DNA lesions leading to mutations associated with BIR. Also, we demonstrate that BIR-associated ssDNA promotes an additional type of genetic instability: replication slippage between microhomologies stimulated by inverted DNA repeats. Based on our results we propose that these events are stimulated by both known sources of ssDNA formed during BIR, nascent DNA formed by leading strand synthesis, and the D-BTS that we describe here. Together we report a new source of mutagenesis during BIR that may also be shared by other homologous recombination pathways driven by D-loop repair synthesis. Oxford University Press 2022-06-24 /pmc/articles/PMC9262586/ /pubmed/35748867 http://dx.doi.org/10.1093/nar/gkac520 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Genome Integrity, Repair and Replication Osia, Beth Twarowski, Jerzy Jackson, Tyler Lobachev, Kirill Liu, Liping Malkova, Anna Migrating bubble synthesis promotes mutagenesis through lesions in its template |
title | Migrating bubble synthesis promotes mutagenesis through lesions in its template |
title_full | Migrating bubble synthesis promotes mutagenesis through lesions in its template |
title_fullStr | Migrating bubble synthesis promotes mutagenesis through lesions in its template |
title_full_unstemmed | Migrating bubble synthesis promotes mutagenesis through lesions in its template |
title_short | Migrating bubble synthesis promotes mutagenesis through lesions in its template |
title_sort | migrating bubble synthesis promotes mutagenesis through lesions in its template |
topic | Genome Integrity, Repair and Replication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9262586/ https://www.ncbi.nlm.nih.gov/pubmed/35748867 http://dx.doi.org/10.1093/nar/gkac520 |
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