Literature DB >> 10368774

Nuclear receptor coregulators: cellular and molecular biology.

N J McKenna1, R B Lanz, B W O'Malley.   

Abstract

Nuclear receptor coregulators are coactivators or corepressors that are required by nuclear receptors for efficient transcripitonal regulation. In this context, we define coactivators, broadly, as molecules that interact with nuclear receptors and enhance their transactivation. Analogously, we refer to nuclear receptor corepressors as factors that interact with nuclear receptors and lower the transcription rate at their target genes. Most coregulators are, by definition, rate limiting for nuclear receptor activation and repression, but do not significantly alter basal transcription. Recent data have indicated multiple modes of action of coregulators, including direct interactions with basal transcription factors and covalent modification of histones and other proteins. Reflecting this functional diversity, many coregulators exist in distinct steady state precomplexes, which are thought to associate in promoter-specific configurations. In addition, these factors may function as molecular gates to enable integration of diverse signal transduction pathways at nuclear receptor-regulated promoters. This review will summarize selected aspects of our current knowledge of the cellular and molecular biology of nuclear receptor coregulators.

Mesh:

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Year:  1999        PMID: 10368774     DOI: 10.1210/edrv.20.3.0366

Source DB:  PubMed          Journal:  Endocr Rev        ISSN: 0163-769X            Impact factor:   19.871


  466 in total

1.  The orphan nuclear receptor Ear-2 is a negative coregulator for thyroid hormone nuclear receptor function.

Authors:  X G Zhu; K S Park; M Kaneshige; M K Bhat; Q Zhu; C N Mariash; P McPhie; S Y Cheng
Journal:  Mol Cell Biol       Date:  2000-04       Impact factor: 4.272

2.  Molecular determinants of nuclear receptor-corepressor interaction.

Authors:  V Perissi; L M Staszewski; E M McInerney; R Kurokawa; A Krones; D W Rose; M H Lambert; M V Milburn; C K Glass; M G Rosenfeld
Journal:  Genes Dev       Date:  1999-12-15       Impact factor: 11.361

3.  Targeted chromatin binding and histone acetylation in vivo by thyroid hormone receptor during amphibian development.

Authors:  L M Sachs; Y B Shi
Journal:  Proc Natl Acad Sci U S A       Date:  2000-11-21       Impact factor: 11.205

4.  Quantitative characterization of the interaction between purified human estrogen receptor alpha and DNA using fluorescence anisotropy.

Authors:  M Boyer; N Poujol; E Margeat; C A Royer
Journal:  Nucleic Acids Res       Date:  2000-07-01       Impact factor: 16.971

5.  Domain structure of the NRIF3 family of coregulators suggests potential dual roles in transcriptional regulation.

Authors:  D Li; F Wang; H H Samuels
Journal:  Mol Cell Biol       Date:  2001-12       Impact factor: 4.272

Review 6.  Resistance to thyroid hormone.

Authors:  R E Weiss; S Refetoff
Journal:  Rev Endocr Metab Disord       Date:  2000-01       Impact factor: 6.514

Review 7.  Thyroid hormone suppression of pituitary hormone gene expression.

Authors:  M A Shupnik
Journal:  Rev Endocr Metab Disord       Date:  2000-01       Impact factor: 6.514

Review 8.  Multiple mechanisms for regulation of the transcriptional activity of thyroid hormone receptors.

Authors:  S Y Cheng
Journal:  Rev Endocr Metab Disord       Date:  2000-01       Impact factor: 6.514

9.  Cdc25B functions as a novel coactivator for the steroid receptors.

Authors:  Z Q Ma; Z Liu; E S Ngan; S Y Tsai
Journal:  Mol Cell Biol       Date:  2001-12       Impact factor: 4.272

Review 10.  Estrogen receptors: orchestrators of pleiotropic cellular responses.

Authors:  J G Moggs; G Orphanides
Journal:  EMBO Rep       Date:  2001-09       Impact factor: 8.807

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