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MUS81-EME2 Promotes Replication Fork Restart

Replication forks frequently stall at regions of the genome that are difficult to replicate or contain lesions that cause replication blockage. An important mechanism for the restart of a stalled fork involves endonucleolytic cleavage that can lead to fork restoration and replication progression. He...

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Detalles Bibliográficos
Autores principales: Pepe, Alessandra, West, Stephen C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5092538/
https://www.ncbi.nlm.nih.gov/pubmed/24813886
http://dx.doi.org/10.1016/j.celrep.2014.04.007
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author Pepe, Alessandra
West, Stephen C.
author_facet Pepe, Alessandra
West, Stephen C.
author_sort Pepe, Alessandra
collection PubMed
description Replication forks frequently stall at regions of the genome that are difficult to replicate or contain lesions that cause replication blockage. An important mechanism for the restart of a stalled fork involves endonucleolytic cleavage that can lead to fork restoration and replication progression. Here, we show that the structure-selective endonuclease MUS81-EME2 is responsible for fork cleavage and restart in human cells. The MUS81-EME2 protein, whose actions are restricted to S phase, is also responsible for telomere maintenance in telomerase-negative ALT (Alternative Lengthening of Telomeres) cells. In contrast, the G2/M functions of MUS81, such as the cleavage of recombination intermediates and fragile site expression, are promoted by MUS81-EME1. These results define distinct and temporal roles for MUS81-EME1 and MUS81-EME2 in the maintenance of genome stability.
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spelling pubmed-50925382016-11-07 MUS81-EME2 Promotes Replication Fork Restart Pepe, Alessandra West, Stephen C. Cell Rep Report Replication forks frequently stall at regions of the genome that are difficult to replicate or contain lesions that cause replication blockage. An important mechanism for the restart of a stalled fork involves endonucleolytic cleavage that can lead to fork restoration and replication progression. Here, we show that the structure-selective endonuclease MUS81-EME2 is responsible for fork cleavage and restart in human cells. The MUS81-EME2 protein, whose actions are restricted to S phase, is also responsible for telomere maintenance in telomerase-negative ALT (Alternative Lengthening of Telomeres) cells. In contrast, the G2/M functions of MUS81, such as the cleavage of recombination intermediates and fragile site expression, are promoted by MUS81-EME1. These results define distinct and temporal roles for MUS81-EME1 and MUS81-EME2 in the maintenance of genome stability. Cell Press 2014-05-09 /pmc/articles/PMC5092538/ /pubmed/24813886 http://dx.doi.org/10.1016/j.celrep.2014.04.007 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Report
Pepe, Alessandra
West, Stephen C.
MUS81-EME2 Promotes Replication Fork Restart
title MUS81-EME2 Promotes Replication Fork Restart
title_full MUS81-EME2 Promotes Replication Fork Restart
title_fullStr MUS81-EME2 Promotes Replication Fork Restart
title_full_unstemmed MUS81-EME2 Promotes Replication Fork Restart
title_short MUS81-EME2 Promotes Replication Fork Restart
title_sort mus81-eme2 promotes replication fork restart
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5092538/
https://www.ncbi.nlm.nih.gov/pubmed/24813886
http://dx.doi.org/10.1016/j.celrep.2014.04.007
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