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Temporal regulation of head-on transcription at replication initiation sites

Head-on (HO) collisions between the DNA replication machinery and RNA polymerase over R-loop forming sequences (RLFS) are genotoxic, leading to replication fork blockage and DNA breaks. Current models suggest that HO collisions are avoided through replication initiation site (RIS) positioning upstre...

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Detalles Bibliográficos
Autores principales: Kronenberg, Michael, Carey, Michael F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9803852/
https://www.ncbi.nlm.nih.gov/pubmed/36594032
http://dx.doi.org/10.1016/j.isci.2022.105791
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author Kronenberg, Michael
Carey, Michael F.
author_facet Kronenberg, Michael
Carey, Michael F.
author_sort Kronenberg, Michael
collection PubMed
description Head-on (HO) collisions between the DNA replication machinery and RNA polymerase over R-loop forming sequences (RLFS) are genotoxic, leading to replication fork blockage and DNA breaks. Current models suggest that HO collisions are avoided through replication initiation site (RIS) positioning upstream of active genes, ensuring co-orientation of replication fork movement and genic transcription. However, this model does not account for pervasive transcription, or intragenic RIS. Moreover, pervasive transcription initiation and CG-rich DNA is a feature of RIS, suggesting that HO transcription units (HO TUs) capable of forming R-loops might occur. Through mining phased GRO-seq data, and developing an informatics strategy to stringently identify RIS, we demonstrate that HO TUs containing RLFS occur at RIS in MCF-7 cells, and are downregulated at the G1/S phase boundary. Our analysis reveals a novel spatiotemporal relationship between transcription and replication, and supports the idea that HO collisions are avoided through transcriptional regulatory mechanisms.
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spelling pubmed-98038522023-01-01 Temporal regulation of head-on transcription at replication initiation sites Kronenberg, Michael Carey, Michael F. iScience Article Head-on (HO) collisions between the DNA replication machinery and RNA polymerase over R-loop forming sequences (RLFS) are genotoxic, leading to replication fork blockage and DNA breaks. Current models suggest that HO collisions are avoided through replication initiation site (RIS) positioning upstream of active genes, ensuring co-orientation of replication fork movement and genic transcription. However, this model does not account for pervasive transcription, or intragenic RIS. Moreover, pervasive transcription initiation and CG-rich DNA is a feature of RIS, suggesting that HO transcription units (HO TUs) capable of forming R-loops might occur. Through mining phased GRO-seq data, and developing an informatics strategy to stringently identify RIS, we demonstrate that HO TUs containing RLFS occur at RIS in MCF-7 cells, and are downregulated at the G1/S phase boundary. Our analysis reveals a novel spatiotemporal relationship between transcription and replication, and supports the idea that HO collisions are avoided through transcriptional regulatory mechanisms. Elsevier 2022-12-10 /pmc/articles/PMC9803852/ /pubmed/36594032 http://dx.doi.org/10.1016/j.isci.2022.105791 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Kronenberg, Michael
Carey, Michael F.
Temporal regulation of head-on transcription at replication initiation sites
title Temporal regulation of head-on transcription at replication initiation sites
title_full Temporal regulation of head-on transcription at replication initiation sites
title_fullStr Temporal regulation of head-on transcription at replication initiation sites
title_full_unstemmed Temporal regulation of head-on transcription at replication initiation sites
title_short Temporal regulation of head-on transcription at replication initiation sites
title_sort temporal regulation of head-on transcription at replication initiation sites
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9803852/
https://www.ncbi.nlm.nih.gov/pubmed/36594032
http://dx.doi.org/10.1016/j.isci.2022.105791
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