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Fork pausing complex engages topoisomerases at the replisome
Replication forks temporarily or terminally pause at hundreds of hard-to-replicate regions around the genome. A conserved pair of budding yeast replisome components Tof1–Csm3 (fission yeast Swi1–Swi3 and human TIMELESS–TIPIN) act as a “molecular brake” and promote fork slowdown at proteinaceous repl...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6938670/ https://www.ncbi.nlm.nih.gov/pubmed/31805522 http://dx.doi.org/10.1101/gad.331868.119 |
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author | Shyian, Maksym Albert, Benjamin Zupan, Andreja Moset Ivanitsa, Vitalii Charbonnet, Gabriel Dilg, Daniel Shore, David |
author_facet | Shyian, Maksym Albert, Benjamin Zupan, Andreja Moset Ivanitsa, Vitalii Charbonnet, Gabriel Dilg, Daniel Shore, David |
author_sort | Shyian, Maksym |
collection | PubMed |
description | Replication forks temporarily or terminally pause at hundreds of hard-to-replicate regions around the genome. A conserved pair of budding yeast replisome components Tof1–Csm3 (fission yeast Swi1–Swi3 and human TIMELESS–TIPIN) act as a “molecular brake” and promote fork slowdown at proteinaceous replication fork barriers (RFBs), while the accessory helicase Rrm3 assists the replisome in removing protein obstacles. Here we show that the Tof1–Csm3 complex promotes fork pausing independently of Rrm3 helicase by recruiting topoisomerase I (Top1) to the replisome. Topoisomerase II (Top2) partially compensates for the pausing decrease in cells when Top1 is lost from the replisome. The C terminus of Tof1 is specifically required for Top1 recruitment to the replisome and fork pausing but not for DNA replication checkpoint (DRC) activation. We propose that forks pause at proteinaceous RFBs through a “sTOP” mechanism (“slowing down with topoisomerases I–II”), which we show also contributes to protecting cells from topoisomerase-blocking agents. |
format | Online Article Text |
id | pubmed-6938670 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-69386702020-07-01 Fork pausing complex engages topoisomerases at the replisome Shyian, Maksym Albert, Benjamin Zupan, Andreja Moset Ivanitsa, Vitalii Charbonnet, Gabriel Dilg, Daniel Shore, David Genes Dev Research Paper Replication forks temporarily or terminally pause at hundreds of hard-to-replicate regions around the genome. A conserved pair of budding yeast replisome components Tof1–Csm3 (fission yeast Swi1–Swi3 and human TIMELESS–TIPIN) act as a “molecular brake” and promote fork slowdown at proteinaceous replication fork barriers (RFBs), while the accessory helicase Rrm3 assists the replisome in removing protein obstacles. Here we show that the Tof1–Csm3 complex promotes fork pausing independently of Rrm3 helicase by recruiting topoisomerase I (Top1) to the replisome. Topoisomerase II (Top2) partially compensates for the pausing decrease in cells when Top1 is lost from the replisome. The C terminus of Tof1 is specifically required for Top1 recruitment to the replisome and fork pausing but not for DNA replication checkpoint (DRC) activation. We propose that forks pause at proteinaceous RFBs through a “sTOP” mechanism (“slowing down with topoisomerases I–II”), which we show also contributes to protecting cells from topoisomerase-blocking agents. Cold Spring Harbor Laboratory Press 2020-01-01 /pmc/articles/PMC6938670/ /pubmed/31805522 http://dx.doi.org/10.1101/gad.331868.119 Text en © 2020 Shyian et al.; 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 | Research Paper Shyian, Maksym Albert, Benjamin Zupan, Andreja Moset Ivanitsa, Vitalii Charbonnet, Gabriel Dilg, Daniel Shore, David Fork pausing complex engages topoisomerases at the replisome |
title | Fork pausing complex engages topoisomerases at the replisome |
title_full | Fork pausing complex engages topoisomerases at the replisome |
title_fullStr | Fork pausing complex engages topoisomerases at the replisome |
title_full_unstemmed | Fork pausing complex engages topoisomerases at the replisome |
title_short | Fork pausing complex engages topoisomerases at the replisome |
title_sort | fork pausing complex engages topoisomerases at the replisome |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6938670/ https://www.ncbi.nlm.nih.gov/pubmed/31805522 http://dx.doi.org/10.1101/gad.331868.119 |
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