| Literature DB >> 24055033 |
Keiji Matsui1, Kasumi Oda, Shumpei Mizuta, Ruri Ishino, Norinaga Urahama, Natsumi Hasegawa, Robert G Roeder, Mitsuhiro Ito.
Abstract
The MED1 subunit of the Mediator transcriptional coregulator complex is a nuclear receptor-specific coactivator. A negative feedback mechanism of thyroid-stimulating hormone (TSH, or thyrotropin) expression in the thyrotroph in the presence of triiodothyronine (T3) is employed by liganded thyroid hormone receptor β (TRβ) on the TSHβ gene promoter, where conventional histone-modifying coactivators act as corepressors. We now provide evidence that MED1 is a ligand-dependent positive cofactor on this promoter. TSHβ gene transcription was attenuated in MED1 mutant mice in which the nuclear receptor-binding ability of MED1 was specifically disrupted. MED1 stimulated GATA2- and Pit1-mediated TSHβ gene promoter activity in a ligand-independent manner in cultured cells. MED1 also stimulated transcription from the TSHβ gene promoter in a T3-dependent manner. The transcription was further enhanced when the T3-dependent corepressors SRC1, SRC2, and HDAC2 were downregulated. Hence, MED1 is a T3-dependent and -independent coactivator on the TSHβ gene promoter.Entities:
Keywords: MED1; Mediator; Negative TR-responsive element; TRβ; TSHβ gene promoter
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Year: 2013 PMID: 24055033 PMCID: PMC4388257 DOI: 10.1016/j.bbrc.2013.09.061
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575