Antagonistic activities of CDC14B and CDK1 on USP9X regulate WT1-dependent mitotic transcription and survival

In yeast, the phosphatase Cdc14 controls mitotic exit. Here the authors show that mammalian CDC14B antagonizes CDK1, to keep the deubiquitinase USP9X unphosphorylated and inactive, and that Wilms’ tumor protein 1 is a substrate for active USP9X that directs mitosis-specific transcription to regulate...

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Main Authors: Michael Dietachmayr, Abirami Rathakrishnan, Oleksandra Karpiuk, Felix von Zweydorf, Thomas Engleitner, Vanesa Fernández-Sáiz, Petra Schenk, Marius Ueffing, Roland Rad, Martin Eilers, Christian Johannes Gloeckner, Katharina Clemm von Hohenberg, Florian Bassermann
Format: Article
Language:English
Published: Nature Publishing Group 2020-03-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-020-15059-5
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spelling doaj-bd16efa5decb42a998a0892197a135452021-05-11T09:09:38ZengNature Publishing GroupNature Communications2041-17232020-03-0111111210.1038/s41467-020-15059-5Antagonistic activities of CDC14B and CDK1 on USP9X regulate WT1-dependent mitotic transcription and survivalMichael Dietachmayr0Abirami Rathakrishnan1Oleksandra Karpiuk2Felix von Zweydorf3Thomas Engleitner4Vanesa Fernández-Sáiz5Petra Schenk6Marius Ueffing7Roland Rad8Martin Eilers9Christian Johannes Gloeckner10Katharina Clemm von Hohenberg11Florian Bassermann12Department of Medicine III, Klinikum rechts der Isar, Technical University of MunichDepartment of Medicine III, Klinikum rechts der Isar, Technical University of MunichDepartment of Medicine III, Klinikum rechts der Isar, Technical University of MunichGerman Center for Neurodegenerative Diseases (DZNE)TranslaTUM, Center for Translational Cancer Research, Technical University of MunichDepartment of Medicine III, Klinikum rechts der Isar, Technical University of MunichDepartment of Medicine III, Klinikum rechts der Isar, Technical University of MunichUniversity of Tübingen, Center for Ophthalmology, Institute for Ophthalmic ResearchTranslaTUM, Center for Translational Cancer Research, Technical University of MunichTheodor Boveri Institute, Department of Biochemistry and Molecular Biology, Biocenter, University of WürzburgGerman Center for Neurodegenerative Diseases (DZNE)Department of Medicine III, Klinikum rechts der Isar, Technical University of MunichDepartment of Medicine III, Klinikum rechts der Isar, Technical University of MunichIn yeast, the phosphatase Cdc14 controls mitotic exit. Here the authors show that mammalian CDC14B antagonizes CDK1, to keep the deubiquitinase USP9X unphosphorylated and inactive, and that Wilms’ tumor protein 1 is a substrate for active USP9X that directs mitosis-specific transcription to regulate mitotic survival.https://doi.org/10.1038/s41467-020-15059-5
collection DOAJ
language English
format Article
sources DOAJ
author Michael Dietachmayr
Abirami Rathakrishnan
Oleksandra Karpiuk
Felix von Zweydorf
Thomas Engleitner
Vanesa Fernández-Sáiz
Petra Schenk
Marius Ueffing
Roland Rad
Martin Eilers
Christian Johannes Gloeckner
Katharina Clemm von Hohenberg
Florian Bassermann
spellingShingle Michael Dietachmayr
Abirami Rathakrishnan
Oleksandra Karpiuk
Felix von Zweydorf
Thomas Engleitner
Vanesa Fernández-Sáiz
Petra Schenk
Marius Ueffing
Roland Rad
Martin Eilers
Christian Johannes Gloeckner
Katharina Clemm von Hohenberg
Florian Bassermann
Antagonistic activities of CDC14B and CDK1 on USP9X regulate WT1-dependent mitotic transcription and survival
Nature Communications
author_facet Michael Dietachmayr
Abirami Rathakrishnan
Oleksandra Karpiuk
Felix von Zweydorf
Thomas Engleitner
Vanesa Fernández-Sáiz
Petra Schenk
Marius Ueffing
Roland Rad
Martin Eilers
Christian Johannes Gloeckner
Katharina Clemm von Hohenberg
Florian Bassermann
author_sort Michael Dietachmayr
title Antagonistic activities of CDC14B and CDK1 on USP9X regulate WT1-dependent mitotic transcription and survival
title_short Antagonistic activities of CDC14B and CDK1 on USP9X regulate WT1-dependent mitotic transcription and survival
title_full Antagonistic activities of CDC14B and CDK1 on USP9X regulate WT1-dependent mitotic transcription and survival
title_fullStr Antagonistic activities of CDC14B and CDK1 on USP9X regulate WT1-dependent mitotic transcription and survival
title_full_unstemmed Antagonistic activities of CDC14B and CDK1 on USP9X regulate WT1-dependent mitotic transcription and survival
title_sort antagonistic activities of cdc14b and cdk1 on usp9x regulate wt1-dependent mitotic transcription and survival
publisher Nature Publishing Group
series Nature Communications
issn 2041-1723
publishDate 2020-03-01
description In yeast, the phosphatase Cdc14 controls mitotic exit. Here the authors show that mammalian CDC14B antagonizes CDK1, to keep the deubiquitinase USP9X unphosphorylated and inactive, and that Wilms’ tumor protein 1 is a substrate for active USP9X that directs mitosis-specific transcription to regulate mitotic survival.
url https://doi.org/10.1038/s41467-020-15059-5
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