Cargando…

ATAD2 is an epigenetic reader of newly synthesized histone marks during DNA replication

ATAD2 (ATPase family AAA domain-containing protein 2) is a chromatin regulator harboring an AAA+ ATPase domain and a bromodomain, previously proposed to function as an oncogenic transcription co-factor. Here we suggest that ATAD2 is also required for DNA replication. ATAD2 is co-expressed with genes...

Descripción completa

Detalles Bibliográficos
Autores principales: Koo, Seong Joo, Fernández-Montalván, Amaury E., Badock, Volker, Ott, Christopher J., Holton, Simon J., von Ahsen, Oliver, Toedling, Joern, Vittori, Sarah, Bradner, James E., Gorjánácz, Mátyás
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342555/
https://www.ncbi.nlm.nih.gov/pubmed/27612420
http://dx.doi.org/10.18632/oncotarget.11855
_version_ 1782513207553818624
author Koo, Seong Joo
Fernández-Montalván, Amaury E.
Badock, Volker
Ott, Christopher J.
Holton, Simon J.
von Ahsen, Oliver
Toedling, Joern
Vittori, Sarah
Bradner, James E.
Gorjánácz, Mátyás
author_facet Koo, Seong Joo
Fernández-Montalván, Amaury E.
Badock, Volker
Ott, Christopher J.
Holton, Simon J.
von Ahsen, Oliver
Toedling, Joern
Vittori, Sarah
Bradner, James E.
Gorjánácz, Mátyás
author_sort Koo, Seong Joo
collection PubMed
description ATAD2 (ATPase family AAA domain-containing protein 2) is a chromatin regulator harboring an AAA+ ATPase domain and a bromodomain, previously proposed to function as an oncogenic transcription co-factor. Here we suggest that ATAD2 is also required for DNA replication. ATAD2 is co-expressed with genes involved in DNA replication in various cancer types and predominantly expressed in S phase cells where it localized on nascent chromatin (replication sites). Our extensive biochemical and cellular analyses revealed that ATAD2 is recruited to replication sites through a direct interaction with di-acetylated histone H4 at K5 and K12, indicative of newly synthesized histones during replication-coupled chromatin reassembly. Similar to ATAD2-depletion, ectopic expression of ATAD2 mutants that are deficient in binding to these di-acetylation marks resulted in reduced DNA replication and impaired loading of PCNA onto chromatin, suggesting relevance of ATAD2 in DNA replication. Taken together, our data show a novel function of ATAD2 in cancer and for the first time identify a reader of newly synthesized histone di-acetylation-marks during replication.
format Online
Article
Text
id pubmed-5342555
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Impact Journals LLC
record_format MEDLINE/PubMed
spelling pubmed-53425552017-03-24 ATAD2 is an epigenetic reader of newly synthesized histone marks during DNA replication Koo, Seong Joo Fernández-Montalván, Amaury E. Badock, Volker Ott, Christopher J. Holton, Simon J. von Ahsen, Oliver Toedling, Joern Vittori, Sarah Bradner, James E. Gorjánácz, Mátyás Oncotarget Research Paper ATAD2 (ATPase family AAA domain-containing protein 2) is a chromatin regulator harboring an AAA+ ATPase domain and a bromodomain, previously proposed to function as an oncogenic transcription co-factor. Here we suggest that ATAD2 is also required for DNA replication. ATAD2 is co-expressed with genes involved in DNA replication in various cancer types and predominantly expressed in S phase cells where it localized on nascent chromatin (replication sites). Our extensive biochemical and cellular analyses revealed that ATAD2 is recruited to replication sites through a direct interaction with di-acetylated histone H4 at K5 and K12, indicative of newly synthesized histones during replication-coupled chromatin reassembly. Similar to ATAD2-depletion, ectopic expression of ATAD2 mutants that are deficient in binding to these di-acetylation marks resulted in reduced DNA replication and impaired loading of PCNA onto chromatin, suggesting relevance of ATAD2 in DNA replication. Taken together, our data show a novel function of ATAD2 in cancer and for the first time identify a reader of newly synthesized histone di-acetylation-marks during replication. Impact Journals LLC 2016-09-06 /pmc/articles/PMC5342555/ /pubmed/27612420 http://dx.doi.org/10.18632/oncotarget.11855 Text en Copyright: © 2016 Koo et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Koo, Seong Joo
Fernández-Montalván, Amaury E.
Badock, Volker
Ott, Christopher J.
Holton, Simon J.
von Ahsen, Oliver
Toedling, Joern
Vittori, Sarah
Bradner, James E.
Gorjánácz, Mátyás
ATAD2 is an epigenetic reader of newly synthesized histone marks during DNA replication
title ATAD2 is an epigenetic reader of newly synthesized histone marks during DNA replication
title_full ATAD2 is an epigenetic reader of newly synthesized histone marks during DNA replication
title_fullStr ATAD2 is an epigenetic reader of newly synthesized histone marks during DNA replication
title_full_unstemmed ATAD2 is an epigenetic reader of newly synthesized histone marks during DNA replication
title_short ATAD2 is an epigenetic reader of newly synthesized histone marks during DNA replication
title_sort atad2 is an epigenetic reader of newly synthesized histone marks during dna replication
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342555/
https://www.ncbi.nlm.nih.gov/pubmed/27612420
http://dx.doi.org/10.18632/oncotarget.11855
work_keys_str_mv AT kooseongjoo atad2isanepigeneticreaderofnewlysynthesizedhistonemarksduringdnareplication
AT fernandezmontalvanamaurye atad2isanepigeneticreaderofnewlysynthesizedhistonemarksduringdnareplication
AT badockvolker atad2isanepigeneticreaderofnewlysynthesizedhistonemarksduringdnareplication
AT ottchristopherj atad2isanepigeneticreaderofnewlysynthesizedhistonemarksduringdnareplication
AT holtonsimonj atad2isanepigeneticreaderofnewlysynthesizedhistonemarksduringdnareplication
AT vonahsenoliver atad2isanepigeneticreaderofnewlysynthesizedhistonemarksduringdnareplication
AT toedlingjoern atad2isanepigeneticreaderofnewlysynthesizedhistonemarksduringdnareplication
AT vittorisarah atad2isanepigeneticreaderofnewlysynthesizedhistonemarksduringdnareplication
AT bradnerjamese atad2isanepigeneticreaderofnewlysynthesizedhistonemarksduringdnareplication
AT gorjanaczmatyas atad2isanepigeneticreaderofnewlysynthesizedhistonemarksduringdnareplication