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Molecular Endocrinology, doi:10.1210/me.2007-0107
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Molecular Endocrinology 21 (12): 2877-2889
Copyright © 2007 by The Endocrine Society

Orphan Receptor TR3 Attenuates the p300-Induced Acetylation of Retinoid X Receptor-{alpha}

Wen-xiu Zhao, Min Tian, Bi-xing Zhao, Gui-deng Li, Bo Liu, Yan-yan Zhan, Hang-zi Chen and Qiao Wu

Key Laboratory of the Ministry of Education for Cell Biology and Tumor Cell Engineering, School of Life Sciences, Xiamen University, Xiamen 361005, Fujian Province, China

Address all correspondence and requests for reprints to: Qiao Wu, Ph.D., Department of Biomedical Sciences, School of Life Sciences, Xiamen University, Xiamen 361005, Fujian, China. E-mail: xgwu{at}xmu.edu.cn.

Acetylation modification regulates the functions of histone and nonhistone proteins, including transcriptional activity, protein interaction, and subcellular localization. Although many nuclear receptors have been shown to be modified by acetylation, whether retinoid X receptors (RXRs) are acetylated and how the acetylation is regulated remains unknown. Here, we provide the first evidence of RXR{alpha} acetylation by p300 on lysine 145. Acetylation of RXR{alpha} by p300 facilitated its DNA binding and subsequently increased its transcriptional activity. Furthermore, we discovered that TR3, an orphan receptor, exerted a negative regulation on p300-induced RXR{alpha} acetylation. TR3 significantly reduced the p300-induced RXR{alpha} acetylation and transcriptional activity, and such inhibition required the interaction of TR3 with RXR{alpha}. Binding of TR3 to RXR{alpha} resulted in the sequestration of RXR{alpha} from p300. 9-cis retinoic acid, a ligand for RXR{alpha}, enhanced the association of RXR{alpha} with TR3, rather than acetylation of RXR{alpha} by p300. Biological function analysis revealed that the mitogenic activity of RXR{alpha} stimulated by p300 was acetylation dependent and could be repressed by TR3. Upon the treatment of 9-cis retinoic acid, RXR{alpha} was translocated with TR3 from the nucleus to the mitochondria, and apoptosis was induced. Taken together, our data demonstrate the distinct regulatory mechanisms of p300 and TR3 on RXR{alpha} acetylation and reveal a previously unrecognized role for orphan receptor in the transcriptional control of retinoid receptors.

NURSA Molecule Pages Link:

Nuclear Receptors:   RXRα  |  RXRβ  |  RXRγ  |  NGFIB
Coregulators:   p300
Ligands:   9-cis-Retinoic acid



This article has been cited by other articles:


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Nucleic Acids ResHome page
N.-z. Lei, X.-y. Zhang, H.-z. Chen, Y. Wang, Y.-y. Zhan, Z.-h. Zheng, Y.-m. Shen, and Q. Wu
A feedback regulatory loop between methyltransferase PRMT1 and orphan receptor TR3
Nucleic Acids Res., February 1, 2009; 37(3): 832 - 848.
[Abstract] [Full Text] [PDF]




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