The ETS Family Member TEL Binds to Nuclear Receptors RAR and RXR and Represses Gene Activation
Author(s) -
Magda A. MeesterSmoor,
Marjolein J. F. W. Janssen,
W. Martijn ter Haar,
Karel H. M. van Wely,
AlbertJan L.H.J. Aarnoudse,
Gertine van Oord,
Gabriëlle B. A. van Tilburg,
Ellen C. Zwarthoff
Publication year - 2011
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0023620
Subject(s) - repressor , retinoid x receptor , nuclear receptor , biology , transcription factor , gene isoform , retinoic acid receptor , psychological repression , retinoic acid , transcriptional regulation , dna binding domain , dna binding protein , regulation of gene expression , microbiology and biotechnology , genetics , gene , gene expression
Retinoic acid receptor (RAR) signaling is important for regulating transcriptional activity of genes involved in growth, differentiation, metabolism and reproduction. Defects in RAR signaling have been implicated in cancer. TEL, a member of the ETS family of transcription factors, is a DNA-binding transcriptional repressor. Here, we identify TEL as a transcriptional repressor of RAR signaling by its direct binding to both RAR and its dimerisation partner, the retinoid x receptor (RXR) in a ligand-independent fashion. TEL is found in two isoforms, created by the use of an alternative startcodon at amino acid 43. Although both isoforms bind to RAR and RXR in vitro and in vivo, the shorter form of TEL represses RAR signaling much more efficiently. Binding studies revealed that TEL binds closely to the DNA binding domain of RAR and that both Helix Loop Helix (HLH) and DNA binding domains of TEL are mandatory for interaction. We have shown that repression by TEL does not involve recruitment of histone deacetylases and suggest that polycomb group proteins participate in the process.
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