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PMID: 11160862 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Rapid polyubiquitination and proteasomal degradation of a mutant form of NAD(P)H:quinone oxidoreductase 1.

Molecular pharmacology ·Vol. 59 ·No. 2 ·2001-02-00 ·Pages 263-8

Siegel D, Anwar A, Winski SL, Kepa JK, Zolman KL, Ross D

Abstract

The NAD(P)H:quinone oxidoreductase 1 (NQO1)*2 polymorphism is characterized by a single proline-to-serine amino acid substitution. Cell lines and tissues from organisms genotyped as homozygous for the NQO1*2 polymorphism are deficient in NQO1 activity. In studies with cells homozygous for the wild-type allele and cells homozygous for the mutant NQO1*2 allele, no difference in the half-life of NQO1 mRNA transcripts was observed. Similarly, in vitro transcription/translation studies showed that both wild-type and mutant NQO1 coding regions were transcribed and translated into full-length protein with equal efficiency. Protein turnover studies in NQO1 wild-type and mutant cell lines demonstrated that the half-life of wild-type NQO1 was greater than 18 h, whereas the half-life of mutant NQO1 was 1.2 h. Incubation of NQO1 mutant cell lines with proteasome inhibitors increased the amount of immunoreactive NQO1 protein, suggesting that mutant protein may be degraded via the proteasome pathway. Additional studies were performed using purified recombinant NQO1 wild-type and mutant proteins incubated in a rabbit reticulocyte lysate system. In these studies, no degradation of wild-type NQO1 protein was observed; however, mutant NQO1 protein was completely degraded in 2 h. Degradation of mutant NQO1 was inhibited by proteasome inhibitors and was ATP-dependent. Mutant NQO1 incubated in rabbit reticulocyte lysate with MG132 resulted in the accumulation of proteins with increased molecular masses that were immunoreactive for both NQO1 and ubiquitin. These data suggest that wild-type NQO1 persists in cells whereas mutant NQO1 is rapidly degraded via ubiquitination and proteasome degradation.

MeSH Terms
Animals Biopolymers/metabolism Caco-2 Cells Cysteine Endopeptidases/metabolism HT29 Cells Humans Multienzyme Complexes/metabolism Mutation Polymorphism, Genetic Proteasome Endopeptidase Complex Quinone Reductases/genetics,metabolism Rabbits Ubiquitins/metabolism
Chemicals
Biopolymers Multienzyme Complexes Ubiquitins NADH dehydrogenase (quinone) Quinone Reductases Cysteine Endopeptidases Proteasome Endopeptidase Complex
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Siegel D
Department of Pharmaceutical Sciences, School of Pharmacy and Cancer Center, University of Colorado Health Sciences Center, Denver, Colorado 80262, USA. [email protected]
Anwar A
Winski S L
Kepa J K
Zolman K L
Ross D
Article Info
Journal
Molecular pharmacology
Abbr.
Mol Pharmacol
ISSN
0026-895X
Published
2001-02-00
Pages
263-8
Language
English
Region
United States
NLM ID
0035623
Subset
IM
Grants
NCI NIH HHS · CA51210 · United States
NCI NIH HHS · CA79446 · United States
NIEHS NIH HHS · ES09554 · United States
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