KAT2A/KAT2B-targeted acetylome reveals a role for PLK4 acetylation in preventing centrosome amplification
The acetyltransferases KAT2A and KAT2B are essential regulators of transcription, cell cycle progression and DNA repair. Here the authors describe a KAT2A/2B-dependent acetylome, and show that acetylation of the protein kinase PLK4 contributes to the regulation of centrosome number.
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2016-10-01
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Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/ncomms13227 |
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doaj-250c67199f71459cb19a3733c6507eda2021-05-11T10:44:52ZengNature Publishing GroupNature Communications2041-17232016-10-017111610.1038/ncomms13227KAT2A/KAT2B-targeted acetylome reveals a role for PLK4 acetylation in preventing centrosome amplificationMarjorie Fournier0Meritxell Orpinell1Cédric Grauffel2Elisabeth Scheer3Jean-Marie Garnier4Tao Ye5Virginie Chavant6Mathilde Joint7Fumiko Esashi8Annick Dejaegere9Pierre Gönczy10László Tora11Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC)Swiss Institute for Experimental Cancer Research (ISREC), School of Life Sciences, Swiss Federal Institute of Technology Lausanne (EPFL)Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC)Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC)Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC)Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC)Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC)Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC)Sir William Dunn School of Pathology, University of OxfordInstitut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC)Swiss Institute for Experimental Cancer Research (ISREC), School of Life Sciences, Swiss Federal Institute of Technology Lausanne (EPFL)Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC)The acetyltransferases KAT2A and KAT2B are essential regulators of transcription, cell cycle progression and DNA repair. Here the authors describe a KAT2A/2B-dependent acetylome, and show that acetylation of the protein kinase PLK4 contributes to the regulation of centrosome number.https://doi.org/10.1038/ncomms13227 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Marjorie Fournier Meritxell Orpinell Cédric Grauffel Elisabeth Scheer Jean-Marie Garnier Tao Ye Virginie Chavant Mathilde Joint Fumiko Esashi Annick Dejaegere Pierre Gönczy László Tora |
spellingShingle |
Marjorie Fournier Meritxell Orpinell Cédric Grauffel Elisabeth Scheer Jean-Marie Garnier Tao Ye Virginie Chavant Mathilde Joint Fumiko Esashi Annick Dejaegere Pierre Gönczy László Tora KAT2A/KAT2B-targeted acetylome reveals a role for PLK4 acetylation in preventing centrosome amplification Nature Communications |
author_facet |
Marjorie Fournier Meritxell Orpinell Cédric Grauffel Elisabeth Scheer Jean-Marie Garnier Tao Ye Virginie Chavant Mathilde Joint Fumiko Esashi Annick Dejaegere Pierre Gönczy László Tora |
author_sort |
Marjorie Fournier |
title |
KAT2A/KAT2B-targeted acetylome reveals a role for PLK4 acetylation in preventing centrosome amplification |
title_short |
KAT2A/KAT2B-targeted acetylome reveals a role for PLK4 acetylation in preventing centrosome amplification |
title_full |
KAT2A/KAT2B-targeted acetylome reveals a role for PLK4 acetylation in preventing centrosome amplification |
title_fullStr |
KAT2A/KAT2B-targeted acetylome reveals a role for PLK4 acetylation in preventing centrosome amplification |
title_full_unstemmed |
KAT2A/KAT2B-targeted acetylome reveals a role for PLK4 acetylation in preventing centrosome amplification |
title_sort |
kat2a/kat2b-targeted acetylome reveals a role for plk4 acetylation in preventing centrosome amplification |
publisher |
Nature Publishing Group |
series |
Nature Communications |
issn |
2041-1723 |
publishDate |
2016-10-01 |
description |
The acetyltransferases KAT2A and KAT2B are essential regulators of transcription, cell cycle progression and DNA repair. Here the authors describe a KAT2A/2B-dependent acetylome, and show that acetylation of the protein kinase PLK4 contributes to the regulation of centrosome number. |
url |
https://doi.org/10.1038/ncomms13227 |
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