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Top1 and Top2 promote replication fork arrest at a programmed pause site

Programmed fork pausing is a complex process allowing cells to arrest replication forks at specific loci in a polar manner. Studies in budding yeast and other model organisms indicate that such replication fork barriers do not act as roadblocks passively impeding fork progression but rather elicit c...

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Autores principales: Larcher, Mélanie V., Pasero, Philippe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6938665/
https://www.ncbi.nlm.nih.gov/pubmed/31896687
http://dx.doi.org/10.1101/gad.335463.119
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author Larcher, Mélanie V.
Pasero, Philippe
author_facet Larcher, Mélanie V.
Pasero, Philippe
author_sort Larcher, Mélanie V.
collection PubMed
description Programmed fork pausing is a complex process allowing cells to arrest replication forks at specific loci in a polar manner. Studies in budding yeast and other model organisms indicate that such replication fork barriers do not act as roadblocks passively impeding fork progression but rather elicit complex interactions between fork and barrier components. In this issue of Genes & Development, Shyian and colleagues (pp. 87–98) show that in budding yeast, the fork protection complex Tof1–Csm3 interacts physically with DNA topoisomerase I (Top1) at replication forks through the C-terminal domain of Tof1. Fork pausing at the ribosomal DNA (rDNA) replication fork barrier (RFB) is impaired in the absence of Top1 or in a tof1 mutant that does not bind Top1, but the function of Top1 can be partially compensated for by Top2. Together, these data indicate that topoisomerases play an unexpected role in the regulation of programmed fork pausing in Saccharomyces cerevisiae.
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spelling pubmed-69386652020-07-01 Top1 and Top2 promote replication fork arrest at a programmed pause site Larcher, Mélanie V. Pasero, Philippe Genes Dev Outlook Programmed fork pausing is a complex process allowing cells to arrest replication forks at specific loci in a polar manner. Studies in budding yeast and other model organisms indicate that such replication fork barriers do not act as roadblocks passively impeding fork progression but rather elicit complex interactions between fork and barrier components. In this issue of Genes & Development, Shyian and colleagues (pp. 87–98) show that in budding yeast, the fork protection complex Tof1–Csm3 interacts physically with DNA topoisomerase I (Top1) at replication forks through the C-terminal domain of Tof1. Fork pausing at the ribosomal DNA (rDNA) replication fork barrier (RFB) is impaired in the absence of Top1 or in a tof1 mutant that does not bind Top1, but the function of Top1 can be partially compensated for by Top2. Together, these data indicate that topoisomerases play an unexpected role in the regulation of programmed fork pausing in Saccharomyces cerevisiae. Cold Spring Harbor Laboratory Press 2020-01-01 /pmc/articles/PMC6938665/ /pubmed/31896687 http://dx.doi.org/10.1101/gad.335463.119 Text en © 2020 Larcher and Pasero; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Outlook
Larcher, Mélanie V.
Pasero, Philippe
Top1 and Top2 promote replication fork arrest at a programmed pause site
title Top1 and Top2 promote replication fork arrest at a programmed pause site
title_full Top1 and Top2 promote replication fork arrest at a programmed pause site
title_fullStr Top1 and Top2 promote replication fork arrest at a programmed pause site
title_full_unstemmed Top1 and Top2 promote replication fork arrest at a programmed pause site
title_short Top1 and Top2 promote replication fork arrest at a programmed pause site
title_sort top1 and top2 promote replication fork arrest at a programmed pause site
topic Outlook
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6938665/
https://www.ncbi.nlm.nih.gov/pubmed/31896687
http://dx.doi.org/10.1101/gad.335463.119
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