| Literature DB >> 25451221 |
Yue Zhao1, Takashi Nomiyama2, Hannes M Findeisen2, Hua Qing1, Jun Aono2, Karrie L Jones2, Elizabeth B Heywood2, Dennis Bruemmer3.
Abstract
The nuclear receptor NOR1 is an immediate-early response gene implicated in the transcriptional control of proliferation. Since the expression level of NOR1 is rapidly induced through cAMP response element binding (CREB) protein-dependent promoter activation, we investigated the contribution of histone acetylation to this transient induction. We demonstrate that NOR1 transcription is induced by histone deacetylase (HDAC) inhibition and by depletion of HDAC1 and HDAC3. HDAC inhibition activated the NOR1 promoter, increased histone acetylation and augmented the recruitment of phosphorylated CREB to the promoter. Furthermore, HDAC inhibition increased Ser133 phosphorylation of CREB and augmented NOR1 protein stability. These data outline previously unrecognized mechanisms of NOR1 regulation and illustrate a key role for histone acetylation in the rapid induction of NOR1.Entities:
Keywords: Histone deacetylase; Nuclear receptor; Smooth muscle cell
Mesh:
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Year: 2014 PMID: 25451221 PMCID: PMC4268421 DOI: 10.1016/j.febslet.2014.11.017
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124