Literature DB >> 18081007

A shifting paradigm: histone deacetylases and transcriptional activation.

Catharine L Smith1.   

Abstract

Transcriptional repression and silencing have been strongly associated with hypoacetylation of histones. Accordingly, histone deacetylases, which remove acetyl groups from histones, have been shown to participate in mechanisms of transcriptional repression. Therefore, current models of the role of acetylation in transcriptional regulation focus on the acetylation status of histones and designate histone acetyltransferases, which add acetyl groups to histones, as transcriptional coactivators and histone deacetylases as corepressors. In recent years, an accumulation of studies have shown that these enzymes also target non-histone proteins and that histone deacetylases have clear roles as coactivators at a variety of genes, some of which are key regulators of cell growth and survival. This review summarizes the evidence for histone deacetylases as coactivators and provides models of coactivation mechanisms, some of which integrate roles of acetylated histones and non-histone proteins in transcription. (c) 2007 Wiley Periodicals, Inc.

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Year:  2008        PMID: 18081007     DOI: 10.1002/bies.20687

Source DB:  PubMed          Journal:  Bioessays        ISSN: 0265-9247            Impact factor:   4.345


  42 in total

1.  Dynamic acetylation of all lysine-4 trimethylated histone H3 is evolutionarily conserved and mediated by p300/CBP.

Authors:  Nicholas T Crump; Catherine A Hazzalin; Erin M Bowers; Rhoda M Alani; Philip A Cole; Louis C Mahadevan
Journal:  Proc Natl Acad Sci U S A       Date:  2011-04-25       Impact factor: 11.205

Review 2.  Histone deacetylases in kidney development: implications for disease and therapy.

Authors:  Shaowei Chen; Samir S El-Dahr
Journal:  Pediatr Nephrol       Date:  2012-06-22       Impact factor: 3.714

3.  Histone deacetylase 9 activates gamma-globin gene expression in primary erythroid cells.

Authors:  Shalini A Muralidhar; Valya Ramakrishnan; Inderdeep S Kalra; Wei Li; Betty S Pace
Journal:  J Biol Chem       Date:  2010-11-13       Impact factor: 5.157

4.  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

5.  Divergent Binding and Transactivation by Two Related Steroid Receptors at the Same Response Element.

Authors:  Martina Tesikova; Xavier Dezitter; Hatice Z Nenseth; Tove I Klokk; Florian Mueller; Gordon L Hager; Fahri Saatcioglu
Journal:  J Biol Chem       Date:  2016-04-07       Impact factor: 5.157

Review 6.  Minireview: The versatile roles of lysine deacetylases in steroid receptor signaling.

Authors:  Vineela Kadiyala; Catharine L Smith
Journal:  Mol Endocrinol       Date:  2014-03-19

7.  Regulation of RNA polymerase II activation by histone acetylation in single living cells.

Authors:  Timothy J Stasevich; Yoko Hayashi-Takanaka; Yuko Sato; Kazumitsu Maehara; Yasuyuki Ohkawa; Kumiko Sakata-Sogawa; Makio Tokunaga; Takahiro Nagase; Naohito Nozaki; James G McNally; Hiroshi Kimura
Journal:  Nature       Date:  2014-09-21       Impact factor: 49.962

8.  CBX7 is a tumor suppressor in mice and humans.

Authors:  Floriana Forzati; Antonella Federico; Pierlorenzo Pallante; Adele Abbate; Francesco Esposito; Umberto Malapelle; Romina Sepe; Giuseppe Palma; Giancarlo Troncone; Marzia Scarfò; Claudio Arra; Monica Fedele; Alfredo Fusco
Journal:  J Clin Invest       Date:  2012-01-03       Impact factor: 14.808

9.  Histone deacetylase 1 and 2 regulate Wnt and p53 pathways in the ureteric bud epithelium.

Authors:  Shaowei Chen; Xiao Yao; Yuwen Li; Zubaida Saifudeen; Dimcho Bachvarov; Samir S El-Dahr
Journal:  Development       Date:  2015-03-15       Impact factor: 6.868

10.  Two histone deacetylases, FfHda1 and FfHda2, are important for Fusarium fujikuroi secondary metabolism and virulence.

Authors:  L Studt; F J Schmidt; L Jahn; C M K Sieber; L R Connolly; E-M Niehaus; M Freitag; H-U Humpf; B Tudzynski
Journal:  Appl Environ Microbiol       Date:  2013-10-04       Impact factor: 4.792

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