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RNase H genes cause distinct impacts on RNA:DNA hybrid formation and mutagenesis genome wide
RNA:DNA hybrids compromise replication fork progression and genome integrity in all cells. 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 investi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10371020/ https://www.ncbi.nlm.nih.gov/pubmed/37494439 http://dx.doi.org/10.1126/sciadv.adi5945 |
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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 compromise replication fork progression and genome integrity in all cells. 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 strongly in noncoding RNAs and 5′-UTRs of coding sequences. For ΔrnhB, hybrids accumulate preferentially in untranslated regions and early in coding sequences. We show that hybrid accumulation is particularly sensitive to gene expression in ΔrnhC cells. DNA replication in ΔrnhC cells is disrupted, leading to transversions and structural variation. Our results resolve the outstanding question of how hybrids in native genomic contexts cause mutagenesis and shape genome organization. |
format | Online Article Text |
id | pubmed-10371020 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-103710202023-07-27 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. Sci Adv Biomedicine and Life Sciences RNA:DNA hybrids compromise replication fork progression and genome integrity in all cells. 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 strongly in noncoding RNAs and 5′-UTRs of coding sequences. For ΔrnhB, hybrids accumulate preferentially in untranslated regions and early in coding sequences. We show that hybrid accumulation is particularly sensitive to gene expression in ΔrnhC cells. DNA replication in ΔrnhC cells is disrupted, leading to transversions and structural variation. Our results resolve the outstanding question of how hybrids in native genomic contexts cause mutagenesis and shape genome organization. American Association for the Advancement of Science 2023-07-26 /pmc/articles/PMC10371020/ /pubmed/37494439 http://dx.doi.org/10.1126/sciadv.adi5945 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). 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 use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences 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 | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10371020/ https://www.ncbi.nlm.nih.gov/pubmed/37494439 http://dx.doi.org/10.1126/sciadv.adi5945 |
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