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PMID: 14712075 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

To be or not to be ubiquitinated?

Cell cycle (Georgetown, Tex.) ·Vol. 3 ·No. 2 ·2004-02-00 ·Pages 138-40

Bloom J, Pagano M

Abstract

Levels of p21, a cyclin-dependent kinase (CDK) inhibitor, are controlled in part at the post-translational level by protein degradation. Although the signaling pathways leading to p21 degradation have not yet been fully elucidated, it is evident that p21 ubiquitination is an essential factor in its degradation. We discuss that, with the only notable exception of ornithine decarboxylase, ubiquitination appears to be a prerequisite for proteasomal degradation rather than an unnecessary byproduct of such proteolysis.

MeSH Terms
Animals Cell Cycle/physiology Cyclin-Dependent Kinase Inhibitor p21 Cyclins/metabolism Cysteine Endopeptidases/metabolism Multienzyme Complexes/metabolism Proteasome Endopeptidase Complex Protein Denaturation/physiology Rabbits Signal Transduction/physiology Ubiquitins/metabolism Ultraviolet Rays
Chemicals
Cyclin-Dependent Kinase Inhibitor p21 Cyclins Multienzyme Complexes Ubiquitins Cysteine Endopeptidases Proteasome Endopeptidase Complex
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Bloom Joanna
Department of Pathology and NYU Cancer Institute, New York University School of Medicine, New York, New York 10016, USA.
Pagano Michele
Article Info
Journal
Cell cycle (Georgetown, Tex.)
Abbr.
Cell Cycle
ISSN
1538-4101
Published
2004-02-00
Pages
138-40
Language
English
Region
United States
NLM ID
101137841
Subset
IM
Grants
NCI NIH HHS · R01-CA76584 · United States
NIGMS NIH HHS · R01-GM57587 · United States
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