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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...

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Autores principales: Osia, Beth, Twarowski, Jerzy, Jackson, Tyler, Lobachev, Kirill, Liu, Liping, Malkova, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
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.
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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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