Literature DB >> 15193452

Nuclear receptor recruitment of histone-modifying enzymes to target gene promoters.

Chih-Cheng Tsai1, Joseph D Fondell.   

Abstract

Nuclear receptors (NRs) compose one of the largest known families of eukaryotic transcription factors and, as such, serve as a paradigm for understanding the fundamental molecular mechanisms of eukaryotic transcriptional regulation. The packaging of eukaryotic genomic DNA into a higher ordered chromatin structure, which generally acts as a barrier to transcription by inhibiting transcription factor accessibility, has a major influence on the mechanisms by which NRs activate or repress gene expression. A major breakthrough in the field's understanding of these mechanisms comes from the recent identification of NR-associated coregulatory factors (i.e., coactivators and corepressors). Although several of these NR cofactors are involved in chromatin remodeling and facilitating the recruitment of the basal transcription machinery, the focus of this chapter is on NR coactivators and corepressors that act to covalently modify the amino-terminal tails of core histones. These modifications (acetylation, methylation, and phosphorylation) are thought to directly affect chromatin structure and?or serve as binding surfaces for other coregulatory proteins. This chapter presents the most current models for NR recruitment of histone-modifying enzymes and then summarizes their functional importance in NR-associated gene expression.

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Year:  2004        PMID: 15193452     DOI: 10.1016/S0083-6729(04)68003-4

Source DB:  PubMed          Journal:  Vitam Horm        ISSN: 0083-6729            Impact factor:   3.421


  24 in total

1.  SMRTε, a corepressor variant, interacts with a restricted subset of nuclear receptors, including the retinoic acid receptors α and β.

Authors:  Brenda J Mengeling; Michael L Goodson; William Bourguet; Martin L Privalsky
Journal:  Mol Cell Endocrinol       Date:  2012-01-12       Impact factor: 4.102

2.  Alternative mRNA splicing of corepressors generates variants that play opposing roles in adipocyte differentiation.

Authors:  Michael L Goodson; Brenda J Mengeling; Brian A Jonas; Martin L Privalsky
Journal:  J Biol Chem       Date:  2011-11-07       Impact factor: 5.157

3.  Repression of cardiac phospholamban gene expression is mediated by thyroid hormone receptor-{alpha}1 and involves targeted covalent histone modifications.

Authors:  Madesh Belakavadi; Jason Saunders; Noah Weisleder; Preethi S Raghava; Joseph D Fondell
Journal:  Endocrinology       Date:  2010-04-14       Impact factor: 4.736

4.  The p160 coactivator PAS-B motif stabilizes nuclear receptor binding and contributes to isoform-specific regulation by thyroid hormone receptors.

Authors:  Martin L Privalsky; Sangho Lee; Johnnie B Hahm; Briana M Young; Rebecca N G Fong; Ivan H Chan
Journal:  J Biol Chem       Date:  2009-06-01       Impact factor: 5.157

5.  Trans-regulation of histone deacetylase activities through acetylation.

Authors:  Yi Luo; Wei Jian; Diana Stavreva; Xueqi Fu; Gordon Hager; Jörg Bungert; Suming Huang; Yi Qiu
Journal:  J Biol Chem       Date:  2009-10-11       Impact factor: 5.157

6.  A mechanism for pituitary-resistance to thyroid hormone (PRTH) syndrome: a loss in cooperative coactivator contacts by thyroid hormone receptor (TR)beta2.

Authors:  Sangho Lee; Briana M Young; Wei Wan; Ivan H Chan; Martin L Privalsky
Journal:  Mol Endocrinol       Date:  2011-05-26

7.  The Neurospora crassa White Collar-1 dependent blue light response requires acetylation of histone H3 lysine 14 by NGF-1.

Authors:  Benedetto Grimaldi; Pierluca Coiro; Patrizia Filetici; Emanuela Berge; Joseph R Dobosy; Michael Freitag; Eric U Selker; Paola Ballario
Journal:  Mol Biol Cell       Date:  2006-08-16       Impact factor: 4.138

8.  DNA recognition by thyroid hormone and retinoic acid receptors: 3,4,5 rule modified.

Authors:  Theresa Q Phan; Margaret M Jow; Martin L Privalsky
Journal:  Mol Cell Endocrinol       Date:  2009-11-27       Impact factor: 4.102

9.  Isoform-specific transcriptional activity of overlapping target genes that respond to thyroid hormone receptors alpha1 and beta1.

Authors:  Ivan H Chan; Martin L Privalsky
Journal:  Mol Endocrinol       Date:  2009-07-23

10.  Thyroid hormone receptor mutants implicated in human hepatocellular carcinoma display an altered target gene repertoire.

Authors:  I H Chan; M L Privalsky
Journal:  Oncogene       Date:  2009-09-14       Impact factor: 9.867

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