Literature DB >> 22967762

Characterization of O-GlcNAc cycling and proteomic identification of differentially O-GlcNAcylated proteins during G1/S transition.

Ludivine Drougat1, Stéphanie Olivier-Van Stichelen, Marlène Mortuaire, François Foulquier, Anne-Sophie Lacoste, Jean-Claude Michalski, Tony Lefebvre, Anne-Sophie Vercoutter-Edouart.   

Abstract

BACKGROUND: DNA replication represents a critical step of the cell cycle which requires highly controlled and ordered regulatory mechanisms to ensure the integrity of genome duplication. Among a plethora of elements, post-translational modifications (PTMs) ensure the spatiotemporal regulation of pivotal proteins orchestrating cell division. Despite increasing evidences showing that O-GlcNAcylation regulates mitotic events, the impact of this PTM in the early steps of the cell cycle remains poorly understood. METHODS AND
RESULTS: Quiescent MCF7 cells were stimulated by serum mitogens and cell cycle progression was determined by flow cytometry. The levels of O-GlcNAc modified proteins, O-GlcNAc Transferase (OGT) and O-GlcNAcase (OGA) were examined by Western blotting and OGA activity was measured during the progression of cells towards S phase. A global decrease in O-GlcNAcylation was observed at S phase entry, concomitantly to an increase in the activity of OGA. A combination of two-dimensional electrophoresis, Western blotting and mass spectrometry was then used to detect and identify cell cycle-dependent putative O-GlcNAcylated proteins. 58 cytoplasmic and nuclear proteins differentially O-GlcNAcylated through G1/S transition were identified and the O-GlcNAc variations of Cytokeratin 8, hnRNP K, Caprin-1, Minichromosome Maintenance proteins MCM3, MCM6 and MCM7 were validated by immunoprecipitation.
CONCLUSIONS: The dynamics of O-GlcNAc is regulated during G1/S transition and observed on key proteins involved in the cytoskeleton networks, mRNA processing, translation, protein folding and DNA replication. GENERAL SIGNIFICANCE: Our results led us to propose that O-GlcNAcylation joins the PTMs that take part in the regulation of DNA replication initiation.
Copyright © 2012 Elsevier B.V. All rights reserved.

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Year:  2012        PMID: 22967762     DOI: 10.1016/j.bbagen.2012.08.024

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  28 in total

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Journal:  Biochem Soc Trans       Date:  2017-04-15       Impact factor: 5.407

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3.  Structures of human O-GlcNAcase and its complexes reveal a new substrate recognition mode.

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Journal:  Nat Struct Mol Biol       Date:  2017-03-20       Impact factor: 15.369

4.  Interaction hot spots for phase separation revealed by NMR studies of a CAPRIN1 condensed phase.

Authors:  Tae Hun Kim; Brandon J Payliss; Michael L Nosella; Ian T W Lee; Yuki Toyama; Julie D Forman-Kay; Lewis E Kay
Journal:  Proc Natl Acad Sci U S A       Date:  2021-06-08       Impact factor: 11.205

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Authors:  Jie Tian; Qizhi Geng; Yuehe Ding; Ji Liao; Meng-Qiu Dong; Xingzhi Xu; Jing Li
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Review 6.  Regulation of protein degradation by O-GlcNAcylation: crosstalk with ubiquitination.

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Journal:  Mol Cell Proteomics       Date:  2013-07-03       Impact factor: 5.911

7.  Combined Antibody/Lectin Enrichment Identifies Extensive Changes in the O-GlcNAc Sub-proteome upon Oxidative Stress.

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Review 8.  Functional O-GlcNAc modifications: implications in molecular regulation and pathophysiology.

Authors:  Krithika Vaidyanathan; Sean Durning; Lance Wells
Journal:  Crit Rev Biochem Mol Biol       Date:  2014-02-14       Impact factor: 8.250

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Journal:  Cell Mol Life Sci       Date:  2021-05-27       Impact factor: 9.261

Review 10.  O-GlcNAc transferase and O-GlcNAcase: achieving target substrate specificity.

Authors:  Alexis K Nagel; Lauren E Ball
Journal:  Amino Acids       Date:  2014-08-31       Impact factor: 3.520

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