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RNase H genes cause distinct impacts on RNA:DNA hybrid formation and mutagenesis genome-wide
RNA:DNA hybrids such as R-loops affect genome integrity and DNA replication fork progression. The overall impacts of naturally occurring RNA:DNA hybrids on genome integrity, and the relative contributions of ribonucleases H to mitigating the negative effects of hybrids, remain unknown. Here, we inve...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197577/ https://www.ncbi.nlm.nih.gov/pubmed/37214986 http://dx.doi.org/10.1101/2023.05.08.539860 |
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author | Schroeder, Jeremy W. Hurto, Rebecca L. Randall, Justin R. Wozniak, Katherine J. Timko, Taylor A. Nye, Taylor M. Wang, Jue D. Freddolino, Peter L. Simmons, Lyle A. |
author_facet | Schroeder, Jeremy W. Hurto, Rebecca L. Randall, Justin R. Wozniak, Katherine J. Timko, Taylor A. Nye, Taylor M. Wang, Jue D. Freddolino, Peter L. Simmons, Lyle A. |
author_sort | Schroeder, Jeremy W. |
collection | PubMed |
description | RNA:DNA hybrids such as R-loops affect genome integrity and DNA replication fork progression. The overall impacts of naturally occurring RNA:DNA hybrids on genome integrity, and the relative contributions of ribonucleases H to mitigating the negative effects of hybrids, remain unknown. Here, we investigate the contributions of RNases HII (RnhB) and HIII (RnhC) to hybrid removal, DNA replication, and mutagenesis genome-wide. Deletion of either rnhB or rnhC triggers RNA:DNA hybrid accumulation, but with distinct patterns of mutagenesis and hybrid accumulation. Across all cells, hybrids accumulate most strongly in non-coding RNAs and 5′-UTRs of coding sequences. For ΔrnhB, hybrids accumulate preferentially in untranslated regions and early in coding sequences. Hybrid accumulation is particularly sensitive to gene expression in ΔrnhC; in cells lacking RnhC, DNA replication is disrupted leading to transversions and structural variation. Our results resolve the outstanding question of how hybrids in native genomic contexts interact with replication to cause mutagenesis and shape genome organization. |
format | Online Article Text |
id | pubmed-10197577 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-101975772023-05-20 RNase H genes cause distinct impacts on RNA:DNA hybrid formation and mutagenesis genome-wide Schroeder, Jeremy W. Hurto, Rebecca L. Randall, Justin R. Wozniak, Katherine J. Timko, Taylor A. Nye, Taylor M. Wang, Jue D. Freddolino, Peter L. Simmons, Lyle A. bioRxiv Article RNA:DNA hybrids such as R-loops affect genome integrity and DNA replication fork progression. The overall impacts of naturally occurring RNA:DNA hybrids on genome integrity, and the relative contributions of ribonucleases H to mitigating the negative effects of hybrids, remain unknown. Here, we investigate the contributions of RNases HII (RnhB) and HIII (RnhC) to hybrid removal, DNA replication, and mutagenesis genome-wide. Deletion of either rnhB or rnhC triggers RNA:DNA hybrid accumulation, but with distinct patterns of mutagenesis and hybrid accumulation. Across all cells, hybrids accumulate most strongly in non-coding RNAs and 5′-UTRs of coding sequences. For ΔrnhB, hybrids accumulate preferentially in untranslated regions and early in coding sequences. Hybrid accumulation is particularly sensitive to gene expression in ΔrnhC; in cells lacking RnhC, DNA replication is disrupted leading to transversions and structural variation. Our results resolve the outstanding question of how hybrids in native genomic contexts interact with replication to cause mutagenesis and shape genome organization. Cold Spring Harbor Laboratory 2023-05-08 /pmc/articles/PMC10197577/ /pubmed/37214986 http://dx.doi.org/10.1101/2023.05.08.539860 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Schroeder, Jeremy W. Hurto, Rebecca L. Randall, Justin R. Wozniak, Katherine J. Timko, Taylor A. Nye, Taylor M. Wang, Jue D. Freddolino, Peter L. Simmons, Lyle A. RNase H genes cause distinct impacts on RNA:DNA hybrid formation and mutagenesis genome-wide |
title | RNase H genes cause distinct impacts on RNA:DNA hybrid formation and mutagenesis genome-wide |
title_full | RNase H genes cause distinct impacts on RNA:DNA hybrid formation and mutagenesis genome-wide |
title_fullStr | RNase H genes cause distinct impacts on RNA:DNA hybrid formation and mutagenesis genome-wide |
title_full_unstemmed | RNase H genes cause distinct impacts on RNA:DNA hybrid formation and mutagenesis genome-wide |
title_short | RNase H genes cause distinct impacts on RNA:DNA hybrid formation and mutagenesis genome-wide |
title_sort | rnase h genes cause distinct impacts on rna:dna hybrid formation and mutagenesis genome-wide |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197577/ https://www.ncbi.nlm.nih.gov/pubmed/37214986 http://dx.doi.org/10.1101/2023.05.08.539860 |
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