Literature DB >> 22989617

The HAT/HDAC interplay: multilevel control of STAT signaling.

Laura Icardi1, Karolien De Bosscher, Jan Tavernier.   

Abstract

Besides the transcription-promoting role of histone acetyltransferases (HATs) and the transcription-delimiting function of histone deacetylases (HDACs) through histone acetylation and deacetylation respectively, HATs and HDACs also regulate the activity of several non-histone proteins. This includes signal transducers and activators of transcription (STATs), key proteins in cytokine signaling. Unlike Tyr phosphorylation/dephosphorylation, which mainly acts as an on/off switch of STAT activity, the control exerted by HATs and HDACs appears multifaceted and far more complex than initially imagined. Our review focuses on the latest trends and novel hypotheses to explain differential context-dependent STAT regulation by complex posttranslational modification patterns. We chart the knowledge on how STATs interact with HATs and HDACs, and additionally bring a transcriptional regulatory and gene-set specific role for HDACs in the picture. Indeed, a growing amount of evidence demonstrates, paradoxically, that not only HAT but also HDAC activity can be required for STAT-dependent transcription, in a STAT subtype- and cell type-dependent manner. Referring to recent reports, we review and discuss the various molecular mechanisms that have recently been proposed to account for this peculiar regulation, in an attempt to shed more light on the difficult yet important question on how STAT specificity is being generated.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22989617     DOI: 10.1016/j.cytogfr.2012.08.002

Source DB:  PubMed          Journal:  Cytokine Growth Factor Rev        ISSN: 1359-6101            Impact factor:   7.638


  17 in total

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2.  Lysine acetyltransferase GCN5 potentiates the growth of non-small cell lung cancer via promotion of E2F1, cyclin D1, and cyclin E1 expression.

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

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Journal:  J Steroid Biochem Mol Biol       Date:  2016-09-16       Impact factor: 4.292

4.  Cross talk between histone deacetylase 4 and STAT6 in the transcriptional regulation of arginase 1 during mouse dendritic cell differentiation.

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Journal:  Mol Cell Biol       Date:  2014-10-20       Impact factor: 4.272

5.  Specific inhibition of histone deacetylase 8 reduces gene expression and production of proinflammatory cytokines in vitro and in vivo.

Authors:  Suzhao Li; Gianluca Fossati; Carlo Marchetti; Daniela Modena; Pietro Pozzi; Leonid L Reznikov; Maria Luisa Moras; Tania Azam; Antonio Abbate; Paolo Mascagni; Charles A Dinarello
Journal:  J Biol Chem       Date:  2014-12-01       Impact factor: 5.157

6.  Nonenzymatic Protein Acetylation Detected by NAPPA Protein Arrays.

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Journal:  ACS Chem Biol       Date:  2015-06-23       Impact factor: 5.100

7.  The expanding roles of neuronal nitric oxide synthase (NOS1).

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Journal:  PeerJ       Date:  2022-07-07       Impact factor: 3.061

Review 8.  Regulation of STAT signaling by acetylation.

Authors:  Shougang Zhuang
Journal:  Cell Signal       Date:  2013-05-22       Impact factor: 4.315

9.  Reciprocal occupancy of BCL6 and STAT5 on Growth Hormone target genes: contrasting transcriptional outcomes and promoter-specific roles of p300 and HDAC3.

Authors:  Grace Lin; Christopher R LaPensee; Zhaohui S Qin; Jessica Schwartz
Journal:  Mol Cell Endocrinol       Date:  2014-08-01       Impact factor: 4.102

Review 10.  The Three Ds of Transcription Activation by Glucagon: Direct, Delayed, and Dynamic.

Authors:  Ido Goldstein; Gordon L Hager
Journal:  Endocrinology       Date:  2018-01-01       Impact factor: 4.736

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