Literature DB >> 16275346

Probing the ubiquitin/proteasome system with ornithine decarboxylase, a ubiquitin-independent substrate.

Martin A Hoyt1, Mingsheng Zhang, Philip Coffino.   

Abstract

Ornithine decarboxylase (ODC) is an unusual proteasome substrate-ubiquitin conjugation plays no part in its turnover. It can therefore be used as a probe to distinguish proteasome-mediated actions that do or do not depend on the activity of the ubiquitin system. A 37 residue region of ODC suffices for proteasome interactions, and within this sequence functionally critical residues have been identified. Because no posttranslational modifications are required for substrate preparation, ODC and derived constructs can be readily generated as substrates for either in vitro or in vivo studies. This chapter describes methodologies that allow the use of ODC as a reporter to examine the ubiquitin-proteasome system, both in reconstituted in vitro systems and in living cells.

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Year:  2005        PMID: 16275346     DOI: 10.1016/S0076-6879(05)98033-6

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  15 in total

1.  Targeted elimination of breast cancer cells with low proteasome activity is sufficient for tumor regression.

Authors:  Erina Vlashi; Chann Lagadec; Mabel Chan; Patricia Frohnen; Alexandra Jean McDonald; Frank Pajonk
Journal:  Breast Cancer Res Treat       Date:  2013-09-08       Impact factor: 4.872

Review 2.  Measuring activity in the ubiquitin-proteasome system: from large scale discoveries to single cells analysis.

Authors:  Adam T Melvin; Gregery S Woss; Jessica H Park; Marcey L Waters; Nancy L Allbritton
Journal:  Cell Biochem Biophys       Date:  2013-09       Impact factor: 2.194

3.  Imaging of radiation effects on cellular 26S proteasome function in situ.

Authors:  James M Brush; Kwanghee Kim; James W Sayre; William H McBride; Keisuke S Iwamoto
Journal:  Int J Radiat Biol       Date:  2009-06       Impact factor: 2.694

4.  Regulation of the proteasome by neuronal activity and calcium/calmodulin-dependent protein kinase II.

Authors:  Stevan N Djakovic; Lindsay A Schwarz; Barbara Barylko; George N DeMartino; Gentry N Patrick
Journal:  J Biol Chem       Date:  2009-07-28       Impact factor: 5.157

5.  Alg13p, the catalytic subunit of the endoplasmic reticulum UDP-GlcNAc glycosyltransferase, is a target for proteasomal degradation.

Authors:  Nicole Averbeck; Xiao-Dong Gao; Shin-Ichiro Nishimura; Neta Dean
Journal:  Mol Biol Cell       Date:  2008-03-12       Impact factor: 4.138

6.  Ubiquitin-independent degradation of p53 mediated by high-risk human papillomavirus protein E6.

Authors:  S Camus; S Menéndez; C F Cheok; L F Stevenson; S Laín; D P Lane
Journal:  Oncogene       Date:  2007-01-15       Impact factor: 9.867

7.  The Ubiquitin-Proteasome System in Huntington's Disease: Are Proteasomes Impaired, Initiators of Disease, or Coming to the Rescue?

Authors:  Sabine Schipper-Krom; Katrin Juenemann; Eric A J Reits
Journal:  Biochem Res Int       Date:  2012-09-24

8.  Enhancement of proteasome activity by a small-molecule inhibitor of USP14.

Authors:  Byung-Hoon Lee; Min Jae Lee; Soyeon Park; Dong-Chan Oh; Suzanne Elsasser; Ping-Chung Chen; Carlos Gartner; Nevena Dimova; John Hanna; Steven P Gygi; Scott M Wilson; Randall W King; Daniel Finley
Journal:  Nature       Date:  2010-09-09       Impact factor: 49.962

9.  Misfolding of proteins with a polyglutamine expansion is facilitated by proteasomal chaperones.

Authors:  Erwann Rousseau; Rieko Kojima; Guylaine Hoffner; Philippe Djian; Anne Bertolotti
Journal:  J Biol Chem       Date:  2008-11-05       Impact factor: 5.157

10.  Failure of amino acid homeostasis causes cell death following proteasome inhibition.

Authors:  Amila Suraweera; Christian Münch; Ariane Hanssum; Anne Bertolotti
Journal:  Mol Cell       Date:  2012-09-06       Impact factor: 17.970

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