Literature DB >> 16634145

Role of the mediator complex in nuclear hormone receptor signaling.

M Belakavadi1, J D Fondell.   

Abstract

Mediator is an evolutionarily conserved multisubunit protein complex that plays a key role in regulating transcription by RNA polymerase II. The complex functions by serving as a molecular bridge between DNA-bound transcriptional activators and the basal transcription apparatus. In humans, Mediator was first characterized as a thyroid hormone receptor (TR)-associated protein (TRAP) complex that facilitates ligand-dependent transcriptional activation by TR. More recently, Mediator has been established as an essential coactivator for a broad range of nuclear hormone receptors (NRs) as well as several other types of gene-specific transcriptional activators. A single subunit of the complex, MED1/TRAP220, is required for direct ligand-dependent interactions with NRs. Mediator coactivates NR-regulated gene expression by facilitating the recruitment and activation of the RNA polymerase II-associated basal transcription apparatus. Importantly, Mediator acts in concert with other NR coactivators involved in chromatin remodeling to initiate transcription of NR target genes in a multistep manner. In this review, we summarize the functional role of Mediator in NR signaling pathways with an emphasis on the underlying molecular mechanisms by which the complex interacts with NRs and subsequently facilitates their action. We also focus on recent advances in our understanding of TRAP/Mediator's pathophysiological role in mammalian disease and development.

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Year:  2006        PMID: 16634145     DOI: 10.1007/s10254-005-0002-0

Source DB:  PubMed          Journal:  Rev Physiol Biochem Pharmacol        ISSN: 0303-4240            Impact factor:   5.545


  37 in total

1.  Specific erythroid-lineage defect in mice conditionally deficient for Mediator subunit Med1.

Authors:  Melanie Stumpf; Xiaojing Yue; Sandra Schmitz; Hervé Luche; Janardan K Reddy; Tilman Borggrefe
Journal:  Proc Natl Acad Sci U S A       Date:  2010-11-23       Impact factor: 11.205

Review 2.  Dynamics of coactivator recruitment and chromatin modifications during nuclear receptor mediated transcription.

Authors:  Sayura Aoyagi; Trevor K Archer
Journal:  Mol Cell Endocrinol       Date:  2007-09-05       Impact factor: 4.102

3.  A muscle-specific knockout implicates nuclear receptor coactivator MED1 in the regulation of glucose and energy metabolism.

Authors:  Wei Chen; Xiaoting Zhang; Kivanc Birsoy; Robert G Roeder
Journal:  Proc Natl Acad Sci U S A       Date:  2010-05-17       Impact factor: 11.205

4.  Cardiac Med1 deletion promotes early lethality, cardiac remodeling, and transcriptional reprogramming.

Authors:  Kathryn M Spitler; Jessica M Ponce; Gavin Y Oudit; Duane D Hall; Chad E Grueter
Journal:  Am J Physiol Heart Circ Physiol       Date:  2017-02-03       Impact factor: 4.733

5.  MED1 phosphorylation promotes its association with mediator: implications for nuclear receptor signaling.

Authors:  Madesh Belakavadi; Pradeep K Pandey; Ravi Vijayvargia; Joseph D Fondell
Journal:  Mol Cell Biol       Date:  2008-04-07       Impact factor: 4.272

Review 6.  An overview of nuclear receptor coregulators involved in cerebellar development.

Authors:  Eijun Nishihara
Journal:  Cerebellum       Date:  2008       Impact factor: 3.847

7.  Common architecture of nuclear receptor heterodimers on DNA direct repeat elements with different spacings.

Authors:  Natacha Rochel; Fabrice Ciesielski; Julien Godet; Edelmiro Moman; Manfred Roessle; Carole Peluso-Iltis; Martine Moulin; Michael Haertlein; Phil Callow; Yves Mély; Dmitri I Svergun; Dino Moras
Journal:  Nat Struct Mol Biol       Date:  2011-04-10       Impact factor: 15.369

8.  Nicotinamide uncouples hormone-dependent chromatin remodeling from transcription complex assembly.

Authors:  Sayura Aoyagi; Trevor K Archer
Journal:  Mol Cell Biol       Date:  2007-10-22       Impact factor: 4.272

Review 9.  Message in a nucleus: signaling to the transcriptional machinery.

Authors:  Inés Carrera; Jessica E Treisman
Journal:  Curr Opin Genet Dev       Date:  2008-08-28       Impact factor: 5.578

10.  A novel androgen receptor-binding element modulates Cdc6 transcription in prostate cancer cells during cell-cycle progression.

Authors:  Feng Jin; Joseph D Fondell
Journal:  Nucleic Acids Res       Date:  2009-06-11       Impact factor: 16.971

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