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Mol. Cell. Biol. 30 (20): 4890-4900

Copyright © 2010 by the American Society for Microbiology. All rights reserved.

Stimulation of Sirt1-Regulated FoxO Protein Function by the Ligand-Bound Vitamin D Receptor{triangledown}

Beum-Soo An,1 Luz E. Tavera-Mendoza,2 Vassil Dimitrov,2 Xiaofeng Wang,1 Mario R. Calderon,1 Hui-Jun Wang,1, and John H. White1,2*

Departments of Physiology,1 Medicine, McGill University, Montreal, Quebec, Canada2

Received for publication 12 February 2010. Revision received 8 April 2010. Accepted for publication 4 August 2010.

Abstract: Hormonal vitamin D, 1,25-dihydroxyvitamin D (1,25D), signals through the nuclear vitamin D receptor (VDR). 1,25D regulates cell proliferation and differentiation and has been identified as a cancer chemopreventive agent. FoxO proteins are transcription factors that control cell proliferation and survival. They function as tumor suppressors and are associated with longevity in several organisms. Accumulating data have revealed that 1,25D and FoxO proteins regulate similarly common target genes. We show here that the ligand-bound VDR regulates the posttranslational modification and function of FoxO proteins. 1,25D treatment enhances binding of FoxO3a and FoxO4 within 4 h to promoters of FoxO target genes and blocks mitogen-induced FoxO protein nuclear export. The VDR associates directly with FoxO proteins and regulators, the sirtuin 1 (Sirt1) class III histone deacetylase (HDAC), and protein phosphatase 1. In addition, phosphatase activity and trichostatin A-resistant HDAC activity coimmunoprecipitate with the VDR. 1,25D treatment rapidly (in <4 h) induces FoxO deacetylation and dephosphorylation, consistent with activation. In contrast, ablation of VDR expression enhances FoxO3a phosphorylation, as does knockdown of Sirt1, consistent with the coupling of FoxO acetylation and phosphorylation. 1,25D regulation of common VDR/FoxO target genes is attenuated by blockade of phosphatase activity or by small interfering RNA (siRNA)-mediated knockdown of Sirt1 or FoxO protein expression. Finally, 1,25D-dependent cell cycle arrest is blocked in FoxO3a-deficient cells, indicating that FoxO proteins are key downstream mediators of the antiproliferative actions of 1,25D. These studies link 1,25D signaling through the VDR directly to Sirt1 and FoxO function and provide a molecular basis for the cancer chemopreventive actions of 1,25D.


* Corresponding author. Mailing address: Department of Physiology, McIntyre Medical Sciences Bldg., Rm. 1112, McGill University, 3655 Drummond St., Montreal, Quebec H3G1Y6, Canada. Phone: (514) 398-8498. Fax: (514) 398-7452. E-mail: john.white{at}mcgill.ca

{triangledown} Published ahead of print on 23 August 2010.



THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Vitamin D receptor as a master regulator of the c-MYC/MXD1 network.
R. Salehi-Tabar, L. Nguyen-Yamamoto, L. E. Tavera-Mendoza, T. Quail, V. Dimitrov, B.-S. An, L. Glass, D. Goltzman, and J. H. White (2012)
PNAS 109, 18827-18832
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