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Regulation of Structure-Specific Endonucleases in Replication Stress

Replication stress results in various forms of aberrant replication intermediates that need to be resolved for faithful chromosome segregation. Structure-specific endonucleases (SSEs) recognize DNA secondary structures rather than primary sequences and play key roles during DNA repair and replicatio...

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Autores principales: Kim, Seong Min, Forsburg, Susan L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316474/
https://www.ncbi.nlm.nih.gov/pubmed/30558228
http://dx.doi.org/10.3390/genes9120634
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author Kim, Seong Min
Forsburg, Susan L.
author_facet Kim, Seong Min
Forsburg, Susan L.
author_sort Kim, Seong Min
collection PubMed
description Replication stress results in various forms of aberrant replication intermediates that need to be resolved for faithful chromosome segregation. Structure-specific endonucleases (SSEs) recognize DNA secondary structures rather than primary sequences and play key roles during DNA repair and replication stress. Holliday junction resolvase MUS81 (methyl methane sulfonate (MMS), and UV-sensitive protein 81) and XPF (xeroderma pigmentosum group F-complementing protein) are a subset of SSEs that resolve aberrant replication structures. To ensure genome stability and prevent unnecessary DNA breakage, these SSEs are tightly regulated by the cell cycle and replication checkpoints. We discuss the regulatory network that control activities of MUS81 and XPF and briefly mention other SSEs involved in the resolution of replication intermediates.
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spelling pubmed-63164742019-01-09 Regulation of Structure-Specific Endonucleases in Replication Stress Kim, Seong Min Forsburg, Susan L. Genes (Basel) Review Replication stress results in various forms of aberrant replication intermediates that need to be resolved for faithful chromosome segregation. Structure-specific endonucleases (SSEs) recognize DNA secondary structures rather than primary sequences and play key roles during DNA repair and replication stress. Holliday junction resolvase MUS81 (methyl methane sulfonate (MMS), and UV-sensitive protein 81) and XPF (xeroderma pigmentosum group F-complementing protein) are a subset of SSEs that resolve aberrant replication structures. To ensure genome stability and prevent unnecessary DNA breakage, these SSEs are tightly regulated by the cell cycle and replication checkpoints. We discuss the regulatory network that control activities of MUS81 and XPF and briefly mention other SSEs involved in the resolution of replication intermediates. MDPI 2018-12-14 /pmc/articles/PMC6316474/ /pubmed/30558228 http://dx.doi.org/10.3390/genes9120634 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Kim, Seong Min
Forsburg, Susan L.
Regulation of Structure-Specific Endonucleases in Replication Stress
title Regulation of Structure-Specific Endonucleases in Replication Stress
title_full Regulation of Structure-Specific Endonucleases in Replication Stress
title_fullStr Regulation of Structure-Specific Endonucleases in Replication Stress
title_full_unstemmed Regulation of Structure-Specific Endonucleases in Replication Stress
title_short Regulation of Structure-Specific Endonucleases in Replication Stress
title_sort regulation of structure-specific endonucleases in replication stress
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316474/
https://www.ncbi.nlm.nih.gov/pubmed/30558228
http://dx.doi.org/10.3390/genes9120634
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