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The corepressor CTBP2 is a coactivator of retinoic acid receptor/ retinoid X receptor in retinoic acid signaling

  • ,
  • Guus J.J.E. Heynen
    ,
  • Lorenza Mittempergher
    ,
  • Wipawadee Grernrum
    ,
  • Iris A.de Rink
    ,
  • Wouter Nijkamp
  • Divisions of Molecular Carcinogenesisa and Genomics Core Facility
    ,
  • Netherlands Cancer Institute
    ,
  • McGill University
Research Output: Contribution to journal Article Peer-review

Open access

Abstract

Retinoids play key roles in development, differentiation, and homeostasis through regulation of specific target genes by the retinoic acid receptor/retinoid X receptor (RAR/RXR) nuclear receptor complex. Corepressors and coactivators contribute to its transcriptional control by creating the appropriate chromatin environment, but the precise composition of these nuclear receptor complexes remains to be elucidated. Using an RNA interference-based genetic screen in mouse F9 cells, we identified the transcriptional corepressor CTBP2 (C-terminal binding protein 2) as a coactivator critically required for retinoic acid (RA)-induced transcription. CTBP2 suppression by RNA interference confers resistance to RA-induced differentiation in diverse murine and human cells. Mechanistically, we find that CTBP2 associates with RAR/RXR at RA target gene promoters and is essential for their transactivation in response to RA. We show that CTBP2 is indispensable to create a chromatin environment conducive for RAR/RXR-mediated transcription by recruiting the histone acetyltransferase p300. Our data reveal an unexpected function of the corepressor CTBP2 as a coactivator for RAR/RXR in RA signaling.

Publication Information

Output type

Research Output: Contribution to journal Article Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 3343-3353 (11 pages)

Journal (Volume, Issue Number)

Molecular and Cellular Biology (Volume 33, Issue 16)

Publication milestones

  • Published - 2013

Publication status

Published - 2013

ISSN

0270-7306

External Publication IDs

  • Scopus: 84881280814
  • PubMed: 23775127