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Pcf1, a large subunit of CAF-1, required for maintenance of checkpoint kinase Cds1 activity

Highly conserved chromatin assembly factor 1 (CAF-1) is required for histone deposition onto newly synthesized DNA to maintain genome stability. This study shows that the fission yeast Pcf1, the large subunit in CAF-1, is crucial for maintaining checkpoint kinase Cds1. Chromatin recruitment of Cds1...

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Detalles Bibliográficos
Autores principales: Kunoh, Tatsuki, Habu, Toshiyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3902073/
https://www.ncbi.nlm.nih.gov/pubmed/24478943
http://dx.doi.org/10.1186/2193-1801-3-30
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author Kunoh, Tatsuki
Habu, Toshiyuki
author_facet Kunoh, Tatsuki
Habu, Toshiyuki
author_sort Kunoh, Tatsuki
collection PubMed
description Highly conserved chromatin assembly factor 1 (CAF-1) is required for histone deposition onto newly synthesized DNA to maintain genome stability. This study shows that the fission yeast Pcf1, the large subunit in CAF-1, is crucial for maintaining checkpoint kinase Cds1. Chromatin recruitment of Cds1 is enhanced by Pcf1 overproduction but is attenuated by the Δpcf1 mutation. Mutation of acetylation sites in the histone H4 tail abrogates the chromatin recruitment of Pcf1, which resembles that of Cds1 as reported previously. The present results provide evidence that chromatin recruitment of Pcf1, moderated by Clr6-HDAC activity, is essential for inactivating Cds1.
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spelling pubmed-39020732014-01-29 Pcf1, a large subunit of CAF-1, required for maintenance of checkpoint kinase Cds1 activity Kunoh, Tatsuki Habu, Toshiyuki Springerplus Research Highly conserved chromatin assembly factor 1 (CAF-1) is required for histone deposition onto newly synthesized DNA to maintain genome stability. This study shows that the fission yeast Pcf1, the large subunit in CAF-1, is crucial for maintaining checkpoint kinase Cds1. Chromatin recruitment of Cds1 is enhanced by Pcf1 overproduction but is attenuated by the Δpcf1 mutation. Mutation of acetylation sites in the histone H4 tail abrogates the chromatin recruitment of Pcf1, which resembles that of Cds1 as reported previously. The present results provide evidence that chromatin recruitment of Pcf1, moderated by Clr6-HDAC activity, is essential for inactivating Cds1. Springer International Publishing 2014-01-17 /pmc/articles/PMC3902073/ /pubmed/24478943 http://dx.doi.org/10.1186/2193-1801-3-30 Text en © Kunoh and Habu; licensee Springer. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Kunoh, Tatsuki
Habu, Toshiyuki
Pcf1, a large subunit of CAF-1, required for maintenance of checkpoint kinase Cds1 activity
title Pcf1, a large subunit of CAF-1, required for maintenance of checkpoint kinase Cds1 activity
title_full Pcf1, a large subunit of CAF-1, required for maintenance of checkpoint kinase Cds1 activity
title_fullStr Pcf1, a large subunit of CAF-1, required for maintenance of checkpoint kinase Cds1 activity
title_full_unstemmed Pcf1, a large subunit of CAF-1, required for maintenance of checkpoint kinase Cds1 activity
title_short Pcf1, a large subunit of CAF-1, required for maintenance of checkpoint kinase Cds1 activity
title_sort pcf1, a large subunit of caf-1, required for maintenance of checkpoint kinase cds1 activity
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3902073/
https://www.ncbi.nlm.nih.gov/pubmed/24478943
http://dx.doi.org/10.1186/2193-1801-3-30
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