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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2014
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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. |
format | Online Article Text |
id | pubmed-5092538 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT pepealessandra mus81eme2promotesreplicationforkrestart AT weststephenc mus81eme2promotesreplicationforkrestart |