Literature DB >> 24645680

Minireview: The versatile roles of lysine deacetylases in steroid receptor signaling.

Vineela Kadiyala1, Catharine L Smith.   

Abstract

Lysine deacetylases have been known to regulate nuclear receptor function for many years. In the unliganded state, nuclear receptors that form heterodimers with retinoid X receptors, such as the retinoic acid and thyroid hormone receptors, associate with deacetylases to repress target genes. In the case of steroid receptors, binding of an antagonist ligand was initially reported to induce association of deacetylases to prevent activation of target genes. Since then, deacetylases have been shown to have diverse functions in steroid receptor signaling, from regulating interactions with molecular chaperones to facilitating their ability to activate transcription. The purpose of this review is to summarize recent studies on the role of deacetylases in steroid receptor signaling, which show deacetylases to be highly versatile regulators of steroid receptor function.

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Year:  2014        PMID: 24645680      PMCID: PMC5414849          DOI: 10.1210/me.2014-1002

Source DB:  PubMed          Journal:  Mol Endocrinol        ISSN: 0888-8809


  125 in total

1.  A 629RKLKK633 motif in the hinge region controls the androgen receptor at multiple levels.

Authors:  Tamzin M Tanner; Sarah Denayer; Bart Geverts; Nora Van Tilborgh; Stefanie Kerkhofs; Christine Helsen; Lien Spans; Vanessa Dubois; Adriaan B Houtsmuller; Frank Claessens; Annemie Haelens
Journal:  Cell Mol Life Sci       Date:  2010-02-26       Impact factor: 9.261

2.  The transcriptional coactivators p300 and CBP are histone acetyltransferases.

Authors:  V V Ogryzko; R L Schiltz; V Russanova; B H Howard; Y Nakatani
Journal:  Cell       Date:  1996-11-29       Impact factor: 41.582

3.  HDAC inhibition attenuates inflammatory, hypertrophic, and hypertensive responses in spontaneously hypertensive rats.

Authors:  Jeffrey P Cardinale; Srinivas Sriramula; Romain Pariaut; Anuradha Guggilam; Nithya Mariappan; Carrie M Elks; Joseph Francis
Journal:  Hypertension       Date:  2010-08-02       Impact factor: 10.190

4.  The expression of a small fraction of cellular genes is changed in response to histone hyperacetylation.

Authors:  C Van Lint; S Emiliani; E Verdin
Journal:  Gene Expr       Date:  1996

5.  Transcriptional activation of estrogen receptor alpha in human breast cancer cells by histone deacetylase inhibition.

Authors:  X Yang; A T Ferguson; S J Nass; D L Phillips; K A Butash; S M Wang; J G Herman; N E Davidson
Journal:  Cancer Res       Date:  2000-12-15       Impact factor: 12.701

6.  Multiple mechanisms induce transcriptional silencing of a subset of genes, including oestrogen receptor alpha, in response to deacetylase inhibition by valproic acid and trichostatin A.

Authors:  George Reid; Raphaël Métivier; Chin-Yo Lin; Stefanie Denger; David Ibberson; Tomi Ivacevic; Heike Brand; Vladimir Benes; Edison T Liu; Frank Gannon
Journal:  Oncogene       Date:  2005-07-21       Impact factor: 9.867

7.  The glucocorticoid receptor controls hepatic dyslipidemia through Hes1.

Authors:  Ulrike Lemke; Anja Krones-Herzig; Mauricio Berriel Diaz; Prachiti Narvekar; Anja Ziegler; Alexandros Vegiopoulos; Andrew C B Cato; Sebastian Bohl; Ursula Klingmüller; Robert A Screaton; Karin Müller-Decker; Sander Kersten; Stephan Herzig
Journal:  Cell Metab       Date:  2008-09       Impact factor: 27.287

8.  Brd4 maintains constitutively active NF-κB in cancer cells by binding to acetylated RelA.

Authors:  Z Zou; B Huang; X Wu; H Zhang; J Qi; J Bradner; S Nair; L-F Chen
Journal:  Oncogene       Date:  2013-05-20       Impact factor: 9.867

9.  Sulforaphane destabilizes the androgen receptor in prostate cancer cells by inactivating histone deacetylase 6.

Authors:  Angela Gibbs; Jacob Schwartzman; Vivianne Deng; Joshi Alumkal
Journal:  Proc Natl Acad Sci U S A       Date:  2009-09-15       Impact factor: 11.205

10.  HDAC1 regulates pluripotency and lineage specific transcriptional networks in embryonic and trophoblast stem cells.

Authors:  Benjamin L Kidder; Stephen Palmer
Journal:  Nucleic Acids Res       Date:  2011-12-10       Impact factor: 16.971

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  3 in total

1.  Class I lysine deacetylases promote glucocorticoid-induced transcriptional repression through functional interaction with LSD1.

Authors:  Nina M Patrick; Chanel A Griggs; Ali L Icenogle; Maryam M Gilpatrick; Vineela Kadiyala; Rosa Jaime-Frias; Catharine L Smith
Journal:  J Steroid Biochem Mol Biol       Date:  2016-09-16       Impact factor: 4.292

2.  Acetylation of lysine 109 modulates pregnane X receptor DNA binding and transcriptional activity.

Authors:  Danielle Pasquel; Aneta Doricakova; Hao Li; Sandhya Kortagere; Matthew D Krasowski; Arunima Biswas; William G Walton; Matthew R Redinbo; Zdenek Dvorak; Sridhar Mani
Journal:  Biochim Biophys Acta       Date:  2016-02-23

3.  LSD1 engages a corepressor complex for the activation of the estrogen receptor α by estrogen and cAMP.

Authors:  Marcela A Bennesch; Gregory Segala; Diana Wider; Didier Picard
Journal:  Nucleic Acids Res       Date:  2016-06-20       Impact factor: 16.971

  3 in total

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