Cited by 260Genomics, phytochemicals, and oxidative stressRedox biology and oxidative stressUbiquitin and proteasome pathways

Physical and functional interaction of sequestosome 1 with Keap1 regulates the Keap1-Nrf2 cell defense pathway

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Copple, Ian M., Lister, Adam, Obeng, Akua D., Kitteringham, Neil R., Jenkins, Rosalind E., Layfield, Robert, Foster, Brian J., Goldring, Christopher E. +1 more·2010·Journal of Biological Chemistry

Abstract

Nrf2 regulates the expression of numerous cytoprotective genes in mammalian cells. The activity of Nrf2 is regulated by the Cul3 adaptor Keap1, yet little is known regarding mechanisms of regulation of Keap1 itself. Here, we have used immunopurification of Keap1 and mass spectrometry, in addition to immunoblotting, to identify sequestosome 1 (SQSTM1) as a cellular binding partner of Keap1. SQSTM1 serves as a scaffold in various signaling pathways and shuttles polyubiquitinated proteins to the proteasomal and lysosomal degradation machineries. Ectopic expression of SQSTM1 led to a decrease in the basal protein level of Keap1 in a panel of cells. Furthermore, RNA interference (RNAi) depletion of SQSTM1 resulted in an increase in the protein level of Keap1 and a concomitant decrease in the protein level of Nrf2 in the absence of changes in Keap1 or Nrf2 mRNA levels. The increased protein level of Keap1 in cells depleted of SQSTM1 by RNAi was linked to a decrease in its rate of degradation; the half-life of Keap1 was almost doubled by RNAi depletion of SQSTM1. The decreased level of Nrf2 in cells depleted of SQSTM1 by RNAi was associated with decreases in the mRNA levels, protein levels, and function of several Nrf2-regulated cell defense genes. SQSTM1 was dispensable for the induction of the Keap1-Nrf2 pathway, as Nrf2 activation by tert-butylhydroquinone or iodoacetamide was not affected by RNAi depletion of SQSTM1. These findings demonstrate a physical and functional interaction between Keap1 and SQSTM1 and reveal an additional layer of regulation in the Keap1-Nrf2 pathway.

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  1. [4]Ramos-Gomez M. Kwak M. K. Dolan P. M. Itoh K. Yamamoto M. Talalay P. Kensler T. W. (2001) Proc. Natl. Acad. Sci. U.S.A. 98, 3410– 3415 11248092 PMC30667
  2. [9]Dinkova-Kostova A. T. Holtzclaw W. D. Cole R. N. Itoh K. Wakabayashi N. Katoh Y. Yamamoto M. Talalay P. (2002) Proc. Natl. Acad. Sci. U.S.A. 99, 11908– 11913 12193649 PMC129367

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Authors
Copple, I. M., Lister, A., Obeng, A. D., Kitteringham, N. R., Jenkins, R. E., Layfield, R., Foster, B. J., Goldring, C. E., & Park, B. K.
Affiliations
  • University of Liverpool (GB)
  • University of Nottingham (GB)
Corresponding author
Goldring, Christopher E.
Venue
Journal of Biological Chemistry
Publisher
Elsevier BV
Published
2010-05
Volume
285
Issue
22
Pages
16782-16788
ISSN
0021-9258 (ISSN-L)
OpenAlex
W2002061608
Cited by
260
References
29
Citations by year
2026: 4 · 2025: 10 · 2024: 20 · 2023: 14 · 2022: 25 · 2021: 30 · 2020: 25 · 2019: 24 · 2018: 7 · 2017: 20 · 2016: 14 · 2015: 9 · 2014: 13 · 2013: 13 · 2012: 19
FWCI
5.86
Type
journal article
Language
en
Open access
Locations
  • Journal of Biological Chemistry (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by-nc)
  • PubMed (publishedVersion)
Funders
Wellcome Trust
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics, phytochemicals, and oxidative stress
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ubiquitin and proteasome pathways
Keywords
p62, Keap1, Nrf2, Nrf2/Keap1 pathway, protein-protein interaction, protein degradation, protein half-life, ubiquitin-proteasome system, lysosomal degradation, cytoprotection, tert-butylhydroquinone, iodoacetamide
MeSH terms
Sequestosome-1 Protein, Kelch-Like ECH-Associated Protein 1, Animals, Cell Line, Gene Expression Regulation, Humans, Lysosomes, Models, Biological, Protein Binding, Signal Transduction, Oxidative Stress, RNA Interference, Proteasome Endopeptidase Complex, Intracellular Signaling Peptides and Proteins, Adaptor Proteins, Signal Transducing, NF-E2-Related Factor 2, Mice

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