1. Academic Validation
  2. Ligand-dependent nuclear receptor corepressor LCoR functions by histone deacetylase-dependent and -independent mechanisms

Ligand-dependent nuclear receptor corepressor LCoR functions by histone deacetylase-dependent and -independent mechanisms

  • Mol Cell. 2003 Jan;11(1):139-50. doi: 10.1016/s1097-2765(03)00014-5.
Isabelle Fernandes 1 Yolande Bastien Timothy Wai Karen Nygard Roberto Lin Olivier Cormier Han S Lee Frankie Eng Nicholas R Bertos Nadine Pelletier Sylvie Mader Victor K M Han Xiang-Jiao Yang John H White
Affiliations

Affiliation

  • 1 Department of Physiology, McGill University, Montreal, Quebec, Canada H3G 1Y6.
Abstract

LCoR (ligand-dependent corepressor) is a transcriptional corepressor widely expressed in fetal and adult tissues that is recruited to agonist-bound nuclear receptors through a single LXXLL motif. LCoR binding to Estrogen Receptor alpha depends in part on residues in the coactivator binding pocket distinct from those bound by TIF-2. Repression by LCoR is abolished by histone deacetylase inhibitor trichostatin A in a receptor-dependent fashion, indicating HDAC-dependent and -independent modes of action. LCoR binds directly to specific HDACs in vitro and in vivo. Moreover, LCoR functions by recruiting C-terminal binding protein corepressors through two consensus binding motifs and colocalizes with CtBPs in the nucleus. LCoR represents a class of corepressor that attenuates agonist-activated nuclear receptor signaling by multiple mechanisms.

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