Literature DB >> 15242341

Gene repression by nuclear hormone receptors.

Udo Moehren1, Maren Eckey, Aria Baniahmad.   

Abstract

Repression by nuclear hormone receptors (NHRs) plays an important role in development, immune response and cellular function. We review mechanisms of how NHRs act as repressors of gene transcription either by direct contact with basal transcription factors or through recruitment of cofactors and enzymic activities that modulate chromatin accessibility. We describe also the role and biochemical mechanism of the cognate hormone that switches a NHR from a transcriptional silencer into an activator. This includes data from crystal structure, functional receptor domain analyses and the role of co-repressors in chromatin modification and remodelling. Furthermore, the comparison of negative response elements with classical response elements unravels the role of co-repressors in this context. We also describe the inhibition of the nuclear factor kappaB and Jun/Fos pathway by NHRs, as well as the molecular mechanism of anti-hormone therapies. Anti-hormones are commonly used in breast and prostate cancer therapy to inhibit cancer proliferation through repression of the oestrogen or androgen receptor, respectively. Here we provide a comprehensive overview of the various mechanism of NHR repression.

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Year:  2004        PMID: 15242341     DOI: 10.1042/bse0400089

Source DB:  PubMed          Journal:  Essays Biochem        ISSN: 0071-1365            Impact factor:   8.000


  15 in total

1.  The highly conserved region of the co-repressor Sin3A functionally interacts with the co-repressor Alien.

Authors:  Udo Moehren; Uwe Dressel; Christina A Reeb; Sami Väisänen; Thomas W Dunlop; Carsten Carlberg; Aria Baniahmad
Journal:  Nucleic Acids Res       Date:  2004-06-01       Impact factor: 16.971

2.  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

3.  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

Review 4.  Structure and function of steroid receptor AF1 transactivation domains: induction of active conformations.

Authors:  Derek N Lavery; Iain J McEwan
Journal:  Biochem J       Date:  2005-11-01       Impact factor: 3.857

5.  Thyroid hormone receptors mutated in liver cancer function as distorted antimorphs.

Authors:  I H Chan; M L Privalsky
Journal:  Oncogene       Date:  2006-01-23       Impact factor: 9.867

6.  Thyroid hormone receptor alpha1 is a critical regulator for the expression of ion channels during final differentiation of outer hair cells.

Authors:  Harald Winter; Claudia Braig; Ulrike Zimmermann; Jutta Engel; Karin Rohbock; Marlies Knipper
Journal:  Histochem Cell Biol       Date:  2007-05-23       Impact factor: 4.304

7.  Estrogen receptors recruit SMRT and N-CoR corepressors through newly recognized contacts between the corepressor N terminus and the receptor DNA binding domain.

Authors:  Natalia Varlakhanova; Chelsea Snyder; Soumia Jose; Johnnie B Hahm; Martin L Privalsky
Journal:  Mol Cell Biol       Date:  2010-01-11       Impact factor: 4.272

8.  Peroxisome proliferator-activated receptor alpha regulates a microRNA-mediated signaling cascade responsible for hepatocellular proliferation.

Authors:  Yatrik M Shah; Keiichirou Morimura; Qian Yang; Tomotaka Tanabe; Mitsuhiro Takagi; Frank J Gonzalez
Journal:  Mol Cell Biol       Date:  2007-04-16       Impact factor: 4.272

9.  Regulation of SMRT corepressor dimerization and composition by MAP kinase phosphorylation.

Authors:  Natalia Varlakhanova; Johnnie B Hahm; Martin L Privalsky
Journal:  Mol Cell Endocrinol       Date:  2010-10-19       Impact factor: 4.102

10.  A conserved lysine in the thyroid hormone receptor-alpha1 DNA-binding domain, mutated in hepatocellular carcinoma, serves as a sensor for transcriptional regulation.

Authors:  Ivan H Chan; Martin L Privalsky
Journal:  Mol Cancer Res       Date:  2010-01-06       Impact factor: 5.852

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