Literature DB >> 23824911

Regulation of protein degradation by O-GlcNAcylation: crosstalk with ubiquitination.

Hai-Bin Ruan1, Yongzhan Nie, Xiaoyong Yang.   

Abstract

The post-translational modification of intracellular proteins by O-linked N-acetylglucosamine (O-GlcNAc) regulates essential cellular processes such as signal transduction, transcription, translation, and protein degradation. Misfolded, damaged, and unwanted proteins are tagged with a chain of ubiquitin moieties for degradation by the proteasome, which is critical for cellular homeostasis. In this review, we summarize the current knowledge of the interplay between O-GlcNAcylation and ubiquitination in the control of protein degradation. Understanding the mechanisms of action of O-GlcNAcylation in the ubiquitin-proteosome system shall facilitate the development of therapeutics for human diseases such as cancer, metabolic syndrome, and neurodegenerative diseases.

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Year:  2013        PMID: 23824911      PMCID: PMC3861702          DOI: 10.1074/mcp.R113.029751

Source DB:  PubMed          Journal:  Mol Cell Proteomics        ISSN: 1535-9476            Impact factor:   5.911


  97 in total

Review 1.  Protein regulation by monoubiquitin.

Authors:  L Hicke
Journal:  Nat Rev Mol Cell Biol       Date:  2001-03       Impact factor: 94.444

Review 2.  p53: death star.

Authors:  K H Vousden
Journal:  Cell       Date:  2000-11-22       Impact factor: 41.582

3.  A glycosylation site, 60SGTS63, of p67 is required for its ability to regulate the phosphorylation and activity of eukaryotic initiation factor 2alpha.

Authors:  Rekha Datta; Papiya Choudhury; Arnab Ghosh; Bansidhar Datta
Journal:  Biochemistry       Date:  2003-05-13       Impact factor: 3.162

4.  Alternative O-glycosylation/O-phosphorylation of serine-16 in murine estrogen receptor beta: post-translational regulation of turnover and transactivation activity.

Authors:  X Cheng; G W Hart
Journal:  J Biol Chem       Date:  2001-01-09       Impact factor: 5.157

Review 5.  A role for N-acetylglucosamine as a nutrient sensor and mediator of insulin resistance.

Authors:  L Wells; K Vosseller; G W Hart
Journal:  Cell Mol Life Sci       Date:  2003-02       Impact factor: 9.261

6.  O-linkage of N-acetylglucosamine to Sp1 activation domain inhibits its transcriptional capability.

Authors:  X Yang; K Su; M D Roos; Q Chang; A J Paterson; J E Kudlow
Journal:  Proc Natl Acad Sci U S A       Date:  2001-05-22       Impact factor: 11.205

7.  26S proteasome subunits are O-linked N-acetylglucosamine-modified in Drosophila melanogaster.

Authors:  Máté Sümegi; Eva Hunyadi-Gulyás; Katalin F Medzihradszky; Andor Udvardy
Journal:  Biochem Biophys Res Commun       Date:  2003-12-26       Impact factor: 3.575

8.  O-GlcNAc modification is an endogenous inhibitor of the proteasome.

Authors:  Fengxue Zhang; Kaihong Su; Xiaoyong Yang; Damon B Bowe; Andrew J Paterson; Jeffrey E Kudlow
Journal:  Cell       Date:  2003-12-12       Impact factor: 41.582

9.  The tumor suppressor HIC1 (hypermethylated in cancer 1) is O-GlcNAc glycosylated.

Authors:  Tony Lefebvre; Sébastien Pinte; Cateline Guérardel; Sophie Deltour; Nathalie Martin-Soudant; Marie-Christine Slomianny; Jean-Claude Michalski; Dominique Leprince
Journal:  Eur J Biochem       Date:  2004-10

10.  Recruitment of O-GlcNAc transferase to promoters by corepressor mSin3A: coupling protein O-GlcNAcylation to transcriptional repression.

Authors:  Xiaoyong Yang; Fengxue Zhang; Jeffrey E Kudlow
Journal:  Cell       Date:  2002-07-12       Impact factor: 41.582

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  59 in total

Review 1.  Hepatic glucose sensing and integrative pathways in the liver.

Authors:  Maaike H Oosterveer; Kristina Schoonjans
Journal:  Cell Mol Life Sci       Date:  2013-11-07       Impact factor: 9.261

Review 2.  Therapeutic Targeting of Epithelial Plasticity Programs: Focus on the Epithelial-Mesenchymal Transition.

Authors:  Reem Malek; Hailun Wang; Kekoa Taparra; Phuoc T Tran
Journal:  Cells Tissues Organs       Date:  2017-02-20       Impact factor: 2.481

3.  Functional Implications of O-GlcNAcylation-dependent Phosphorylation at a Proximal Site on Keratin 18.

Authors:  Poonam S Kakade; Srikanth Budnar; Rajiv D Kalraiya; Milind M Vaidya
Journal:  J Biol Chem       Date:  2016-04-08       Impact factor: 5.157

4.  Systematic characterization and prediction of post-translational modification cross-talk.

Authors:  Yuanhua Huang; Bosen Xu; Xueya Zhou; Ying Li; Ming Lu; Rui Jiang; Tingting Li
Journal:  Mol Cell Proteomics       Date:  2015-01-20       Impact factor: 5.911

5.  O-GlcNAc occurs cotranslationally to stabilize nascent polypeptide chains.

Authors:  Yanping Zhu; Ta-Wei Liu; Samy Cecioni; Razieh Eskandari; Wesley F Zandberg; David J Vocadlo
Journal:  Nat Chem Biol       Date:  2015-03-16       Impact factor: 15.040

Review 6.  Protein O-GlcNAcylation: emerging mechanisms and functions.

Authors:  Xiaoyong Yang; Kevin Qian
Journal:  Nat Rev Mol Cell Biol       Date:  2017-05-10       Impact factor: 94.444

Review 7.  Proteasome Biology: Chemistry and Bioengineering Insights.

Authors:  Lucia Račková; Erika Csekes
Journal:  Polymers (Basel)       Date:  2020-12-04       Impact factor: 4.329

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

9.  Intracellular O-linked glycosylation directly regulates cardiomyocyte L-type Ca2+ channel activity and excitation-contraction coupling.

Authors:  Andrew R Ednie; Eric S Bennett
Journal:  Basic Res Cardiol       Date:  2020-09-10       Impact factor: 17.165

Review 10.  Proteolysis, synaptic plasticity and memory.

Authors:  Ashok N Hegde
Journal:  Neurobiol Learn Mem       Date:  2016-09-07       Impact factor: 2.877

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