SUMO-Based Regulation of Nuclear Positioning to Spatially Regulate Homologous Recombination Activities at Replication Stress Sites

DNA lesions have properties that allow them to escape their nuclear compartment to achieve DNA repair in another one. Recent studies uncovered that the replication fork, when its progression is impaired, exhibits increased mobility when changing nuclear positioning and anchors to nuclear pore comple...

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Main Authors: Kamila Schirmeisen, Sarah A. E. Lambert, Karol Kramarz
Format: Article
Language:English
Published: MDPI AG 2021-12-01
Series:Genes
Subjects:
Online Access:https://www.mdpi.com/2073-4425/12/12/2010
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author Kamila Schirmeisen
Sarah A. E. Lambert
Karol Kramarz
author_facet Kamila Schirmeisen
Sarah A. E. Lambert
Karol Kramarz
author_sort Kamila Schirmeisen
collection DOAJ
description DNA lesions have properties that allow them to escape their nuclear compartment to achieve DNA repair in another one. Recent studies uncovered that the replication fork, when its progression is impaired, exhibits increased mobility when changing nuclear positioning and anchors to nuclear pore complexes, where specific types of homologous recombination pathways take place. In yeast models, increasing evidence points out that nuclear positioning is regulated by small ubiquitin-like modifier (SUMO) metabolism, which is pivotal to maintaining genome integrity at sites of replication stress. Here, we review how SUMO-based pathways are instrumental to spatially segregate the subsequent steps of homologous recombination during replication fork restart. In particular, we discussed how routing towards nuclear pore complex anchorage allows distinct homologous recombination pathways to take place at halted replication forks.
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spelling doaj.art-e29c9c6dc69d458fbea1a6d88a1163f62023-11-23T08:31:38ZengMDPI AGGenes2073-44252021-12-011212201010.3390/genes12122010SUMO-Based Regulation of Nuclear Positioning to Spatially Regulate Homologous Recombination Activities at Replication Stress SitesKamila Schirmeisen0Sarah A. E. Lambert1Karol Kramarz2Institut Curie, Université PSL, CNRS UMR3348, 91400 Orsay, FranceInstitut Curie, Université PSL, CNRS UMR3348, 91400 Orsay, FranceAcademic Excellence Hub—Research Centre for DNA Repair and Replication, University of Wrocław, 50-328 Wrocław, PolandDNA lesions have properties that allow them to escape their nuclear compartment to achieve DNA repair in another one. Recent studies uncovered that the replication fork, when its progression is impaired, exhibits increased mobility when changing nuclear positioning and anchors to nuclear pore complexes, where specific types of homologous recombination pathways take place. In yeast models, increasing evidence points out that nuclear positioning is regulated by small ubiquitin-like modifier (SUMO) metabolism, which is pivotal to maintaining genome integrity at sites of replication stress. Here, we review how SUMO-based pathways are instrumental to spatially segregate the subsequent steps of homologous recombination during replication fork restart. In particular, we discussed how routing towards nuclear pore complex anchorage allows distinct homologous recombination pathways to take place at halted replication forks.https://www.mdpi.com/2073-4425/12/12/2010DNAreplication stressSUMOgenome stabilityhomologous recombinationnuclear pore complex
spellingShingle Kamila Schirmeisen
Sarah A. E. Lambert
Karol Kramarz
SUMO-Based Regulation of Nuclear Positioning to Spatially Regulate Homologous Recombination Activities at Replication Stress Sites
Genes
DNA
replication stress
SUMO
genome stability
homologous recombination
nuclear pore complex
title SUMO-Based Regulation of Nuclear Positioning to Spatially Regulate Homologous Recombination Activities at Replication Stress Sites
title_full SUMO-Based Regulation of Nuclear Positioning to Spatially Regulate Homologous Recombination Activities at Replication Stress Sites
title_fullStr SUMO-Based Regulation of Nuclear Positioning to Spatially Regulate Homologous Recombination Activities at Replication Stress Sites
title_full_unstemmed SUMO-Based Regulation of Nuclear Positioning to Spatially Regulate Homologous Recombination Activities at Replication Stress Sites
title_short SUMO-Based Regulation of Nuclear Positioning to Spatially Regulate Homologous Recombination Activities at Replication Stress Sites
title_sort sumo based regulation of nuclear positioning to spatially regulate homologous recombination activities at replication stress sites
topic DNA
replication stress
SUMO
genome stability
homologous recombination
nuclear pore complex
url https://www.mdpi.com/2073-4425/12/12/2010
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AT karolkramarz sumobasedregulationofnuclearpositioningtospatiallyregulatehomologousrecombinationactivitiesatreplicationstresssites