Faculty & Staff Directory > John White


Faculty & Staff Directory

 

John White - Professor

Department of Physiology
McGill University
McIntyre Medical Sciences Building,
Room 1128
3655 Promenade Sir William Osler
Montréal, Québec H3G 1Y6

(514) 398-8498

john.white@mcgill.ca

Laboratory web site:
www.physio.mcgill.ca/whitelab

Research Area:  Cell and Molecular Biology

Research Description:

The laboratory has focused since its inception on various aspects of regulation of gene expression. Much of the work centers on the role of nuclear receptors in controlling gene transcription. The lab has been interested in the molecular mechanisms of action of estrogen receptors (ERs) for several years, and has identified novel coregulatory factors that control the nuclear and extra-nuclear functions actions of ERs and other nuclear receptors. The laboratory is also studying the genomics of nuclear receptor action. The lab is analyzing the potential roles of target genes of the vitamin D3 receptor in controlling the growth of cancer cells. We have identified almost 200 vitamin D3 target genes in squamous carcinoma cells by microarray analysis, and are determining the functions of key genes in regulation of cellular growth and differentiation.

Education:  B.Sc., M.Sc., Carleton, Ph.D., Harvard

Recent Publications:
(and PDF file links)

Nuclear localization of LCoR in MCF-7 cells.


Prudencio, J. Akutsu, N., Wong, T., Bastien, Y., Lin, R., Black, M.J., Alaoui-Jamali, M. and White, J.H. (2001)
Action of low calcemic 1,25-dihydroxyvitamin D3 analog EB1089 in head and neck squamous cell carcinoma. J. Nat. Cancer Inst. 93, 745-53.

Akutsu, N., Lin, R., Bastien, Y., Bestawros, A., Enepekides, D.J., Black, M.J. and White, J.H. (2001)
Regulation of Gene Expression by 1α,25-dihydroxyvitamin D3 and its Analog EB1089 under Growth Inhibitory Conditions in Squamous Carcinoma Cells. Mol. Endocrinol. 15, 1127-39.

Lin, R., Nagai, Y., Sladek, R., Bastien, Y., Ho, J., Petrecca, K., Sotiropoulou, G., Diamandis, E.P., Hudson, T., and White J.H. (2002)
Expression profiling in squamous carcinoma cells reveals pleiotropic effects of vitamin D3 signaling on cell proliferation, differentiation and immune system regulation. Mol. Endocrinol. 16, 1243-56.

Fernandes, I, Bastien, Y., Wai, T., Nygard, K., Lin, R., Cormier, O., Lee, H.S., Eng, F., Bertos, N.R., Pelletier, N., Mader, S., Han V.K.M., Yang, X.J. and White, J.H. (2003) Ligand-dependent corepressor LCoR functions by histone deacetylase-dependent and –independent mechanisms. Molecular Cell, 11, 139-50.
(Supplemental text & figs;
http://download.molecule.org/pdfs/1097-2765/PIIS1097276503000145.pdf )

Bourdeau, V., Deschenes, J., Metivier, R., Nagai, Y., Nguyen, D., Bretschneider, N., Gannon, F., White, J.H. and Mader S. (2004)
Genome-wide identification of high affinity estrogen response elements in human and mouse. Mol. Endocrinol. 18, 1411-1427.

Wang, T.T., Nestel, F., Bourdeau, V., Nagai, Y., Wang, Q., Wu, J., Tavera-Mendoza, L., Lin, R., Hanrahan, J.H., Mader, S. and White, J.H. (2004)
1,25-dihydroxyvitamin D3 is a direct inducer of antimicrobial peptide gene expression. J. Immunol. (Cutting Edge Report). 173, 2909-12.

Wang, T.T., Tavera-Mendoza, L., Laperriere, D., Nagai, Y., Burton MacLeod, N., Libby, E., Zhang, R., Bourdeau, V., Konstorum, A., Lallemant, B., Mader, S. and White, J.H. (2005)
Large-scale in silico and microarray-based genomic screening of 1,25-dihydroxyvitamin D3 target genes. Mol. Endocrinol. 19, 2685-95.

Tavera-Mendoza, L., Wang, T.T., Lallemant, B., Zhang, R., Nagai, Y., Bourdeau, V., Ramiro Calderon, M., Desbarats, J., Mader, S., and White, J.H. (2006)
Convergence of vitamin D and retinoic acid signaling at a common hormone response element. EMBO Rep. 7, 180-185. (Suppl. material; www.nature.com/embor/journal/v7/n2/suppinfo/7400594.html).

Tavera-Mendoza LE, White JH.
Cell defenses and the sunshine vitamin. Sci Am. 2007 Nov; 297(5):62-5, 68-70, 72.


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