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Epitranscriptomics & Cancer Adaptation : A.David

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Our research work focuses on the contribution of post-transcriptional mechanisms on cancer cell adaptation, in particular RNA epigenetic & translational control.

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Added by eric_julien
Group name EquipeEJ
Item Type Journal Article
Title Kizuna is a novel mitotic substrate for CDC25B phosphatase
Creator Thomas et al.
Author Yann Thomas
Author Marion Peter
Author Francisca Mechali
Author Jean-Marie Blanchard
Author Olivier Coux
Author Véronique Baldin
Abstract CDC25 dual-specificity phosphatases play a central role in cell cycle control through the activation of Cyclin-Dependent Kinases (CDKs). Expression during mitosis of a stabilized CDC25B mutant (CDC25B-DDA), which cannot interact with the F-box protein ?TrCP for proteasome-dependent degradation, causes mitotic defects and chromosome segregation errors in mammalian cells. We found, using the same CDC25B mutant, that stabilization and failure to degrade CDC25B during mitosis lead to the appearance of multipolar spindle cells resulting from a fragmentation of pericentriolar material (PCM) and abolish mitotic Plk1-dependent phosphorylation of Kizuna (Kiz), which is essential for the function of Kiz in maintaining spindle pole integrity. Thus, in mitosis Kiz is a new substrate of CDC25B whose dephosphorylation following CDC25B stabilization leads to the formation of multipolar spindles. Furthermore, endogenous Kiz and CDC25B interact only in mitosis, suggesting that Kiz phosphorylation depends on a balance between CDC25B and Plk1 activities. Our data identify a novel mitotic substrate of CDC25B phosphatase that plays a key role in mitosis control.
Publication Cell Cycle (Georgetown, Tex.)
Volume 13
Issue 24
Pages 3867-3877
Date 2014
Journal Abbr Cell Cycle
Language eng
DOI 10.4161/15384101.2014.972882
ISSN 1551-4005
Library Catalog PubMed
Extra PMID: 25558830 PMCID: PMC4615109
Tags cdc25 Phosphatases, CDC25B, Cell Cycle Proteins, Cell Line, Tumor, Centrosome, DMSO, dimethyl-sulfoxyde, DSP, Dithiobis [succinimidyl propionate], first-last-corresponding, HeLa Cells, Humans, Kiz, Kizuna protein, Kizuna, mitosis, Mutation, original, PCM, pericentriolar material, Phosphorylation, Protein-Serine-Threonine Kinases, Proto-Oncogene Proteins, Recombinant Fusion Proteins, Spindle Apparatus
Date Added 2019/05/28 - 13:52:21
Date Modified 2019/05/28 - 13:58:20
Notes and Attachments PubMed entry (Attachment)
Texte intégral (Attachment)


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