Two domains of Nrf2 cooperatively bind CBP, a CREB binding protein, and synergistically activate transcription

Yasutake Katoh, Ken Itoh, Eisaku Yoshida, Makoto Miyagishi, Akiyoshi Fukamizu, Masayuki Yamamoto

Research output: Contribution to journalArticlepeer-review

292 Citations (Scopus)

Abstract

Background: Nrf2 belongs to the Cap-N-Collar (CNC) transcription factor family and is essential for the antioxidant responsive element (ARE)-mediated expression of a group of detoxifying and antioxidant genes. The forced expression of Nrf2 in mammalian cells activates the expression of target genes through the ARE, with Nrf2 showing the highest transactivation activity among the CNC family of transcription factors. To elucidate the molecular mechanisms generating this potent transactivation activity, we examined the functions of the domains within Nrf2. Result: We found that Nrf2 contains two transcription activation domains, Neh4 and Neh5, which act synergistically to attain maximum a activation of reporter gene expression. Neh4 and Neh5 both individually and cooperatively bind to CBP (CREB (cAMP Responsive Element Binding protein) Binding Protein). In fact, the specific inhibitor of CBP, adenovirus E1A protein, significantly reduced Nrf2 activity. Importantly, the CBP-binding activity of Nrf2 deletion mutants positively correlated with their transactivation activity. Neh5 contains a motif which is commonly conserved among the CNC factors, whereas Neh4 contains the novel CBP-interacting motif recently identified in p53 and E2F. Conclusions: Our results indicate that Nrf2 exploits the cooperative binding of two independent transactivation domains to CBP in the acquisition of a potent transactivation activity.

Original languageEnglish
Pages (from-to)857-868
Number of pages12
JournalGenes to Cells
Volume6
Issue number10
DOIs
Publication statusPublished - 2001

ASJC Scopus subject areas

  • Genetics
  • Cell Biology

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