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Epigenetic regulation of the NR4A orphan nuclear receptor NOR1 by histone acetylation
被引:7
|作者:
Zhao, Yue
[1
,2
]
Nomiyama, Takashi
[1
]
Findeisen, Hannes M.
[1
]
Qing, Hua
[1
,2
]
Aono, Jun
[1
]
Jones, Karrie L.
[1
]
Heywood, Elizabeth B.
[1
]
Bruemmer, Dennis
[1
,2
]
机构:
[1] Univ Kentucky, Saha Cardiovasc Res Ctr, BBSRB, Lexington, KY 40536 USA
[2] Univ Kentucky, Grad Ctr Nutr Sci, Lexington, KY 40536 USA
关键词:
Nuclear receptor;
Smooth muscle cell;
Histone deacetylase;
MUSCLE-CELL PROLIFERATION;
PHOSPHORYLATION;
TRANSCRIPTION;
EXPRESSION;
INHIBITION;
DEFICIENCY;
ACTIVATION;
CHROMATIN;
NUR77;
GENE;
D O I:
10.1016/j.febslet.2014.11.017
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
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. (C) 2014 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
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页码:4825 / 4830
页数:6
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