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Induction of cereblon by NF-E2-related factor 2 in neuroblastoma cells exposed to hypoxia-reoxygenation.

Abstract
Cereblon is a protein encoded by the CRBN gene, which has been associated with human autosomal recessive nonsyndromic mental retardation. However, little is known about the regulation of CRBN expression. Following exposure of mouse neuroblastoma N2A cells to hypoxia/reoxygenation (H/R), mRNA and protein expression of CRBN were increased. To better understand how CRBN expression is regulated, the promoter region of the mouse CRBN gene was characterized functionally. Deletion mutations and site-directed mutagenesis led to the identification of a functional NF-E2-related factor 2 (Nrf2)-binding site. Electrophoretic mobility shift analysis indicated that Nrf2 binds to a putative binding site in the CRBN promoter. Nrf2 overexpression and tert-butylhydroquinone treatment enhanced CRBN protein expression. These results imply that Nrf2 stimulates CRBN gene transcription under H/R conditions in neuronal cells.
AuthorsKyung Jin Lee, Kwang Min Lee, Sooyeon Jo, Keon Wook Kang, Chul-Seung Park
JournalBiochemical and biophysical research communications (Biochem Biophys Res Commun) Vol. 399 Issue 4 Pg. 711-5 (Sep 03 2010) ISSN: 1090-2104 [Electronic] United States
PMID20691658 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright 2010 Elsevier Inc. All rights reserved.
Chemical References
  • Adaptor Proteins, Signal Transducing
  • Crbn protein, mouse
  • Hydroquinones
  • NF-E2-Related Factor 2
  • Nerve Tissue Proteins
  • 2-tert-butylhydroquinone
  • Oxygen
Topics
  • Adaptor Proteins, Signal Transducing
  • Animals
  • Cell Hypoxia
  • Cell Line, Tumor
  • Electrophoretic Mobility Shift Assay
  • Gene Deletion
  • Hydroquinones (pharmacology)
  • Intellectual Disability (genetics)
  • Mice
  • Mutagenesis, Site-Directed
  • NF-E2-Related Factor 2 (metabolism)
  • Nerve Tissue Proteins (genetics)
  • Neurons (drug effects, metabolism)
  • Oxygen (metabolism)
  • Promoter Regions, Genetic
  • Response Elements

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