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Glenville Jones

 
  Vitamin Metabolism

 
  Contact Information:  
  Professor of Biochemistry & Medicine
B.Sc., Ph.D., Liverpool, U.K.;
Postdoctoral Fellow, University of Calgary & University of Wisconsin-Madison;
Associate Professor of Biochemistry, Hospital for Sick Children-Research Institute & University of Toronto;
Visiting Professor, University of Arizona

Tel: (613) 533-2498
Fax: (613) 533-2987
email: gj1@post.queensu.ca


 
  Vitamins D and A are now recognized to be precursors to the hormones, calcitriol (1,25-dihydroxyvitamin D3) and retinoic acid, respectively. Both hormones, acting through specific transcription factors are potent cell-differentiating agents and in addition, calcitriol regulates the plasma level of calcium. My laboratory utilizes unique in vitro cultured cell or transfected cell models to study the activation or breakdown of calcitriol or retinoic acid. Among the biological actions of calcitriol and retinoic acid is the ability to induce their own catabolic enzymes. The long-term aim of our research is to establish the structure and function of the cytochrome P-450 enzymes involved in the complex metabolic pathways of calcitriol or retinoic acid and thus the role of these enzymes in the regulation of extracellular calcium homeostasis and cell differentiation at the whole organism level.

Recently, we have successfully elucidated the complex pattern of catabolism of calcitriol to calcitroic acid and retinoic acid to 4-hydroxy retinoic acid occurring inside target cells. Currently, utilising collaborations with partners from the pharmaceutical industry, we are applying this basic knowledge to the study of the metabolism of several new vitamin D analogs (see Figure 1), under development around the world for the treatment of osteoporosis, psoriasis and cancer. In the course of this work, we are using vitamin D analogs as probes in structure/activity studies to explore the specificity of the substrate-binding pocket of the cytochrome P-450 isoforms involved in vitamin D metabolism. We have cloned the cDNA's and genes for two of these cytochromes, and are presently using mammalian and bacterial expression systems containing the cDNA's encoding these P-450's in studies aimed at pinpointing the location of the vitamin D-binding, ferridoxin-binding and heme-binding domains. Molecular modelling (Figure 2) and site-directed mutagenesis studies of the cytochrome P-450's are also underway. It is expected that these studies will not only reveal useful basic information about the structure and mechanism of catalysis of cytochrome P-450's but will also lead to rational vitamin D and retinoid drug design in the future.



 
  Publications:  
  Dilworth F.J., Williams G.R., Kissmeyer A-M, L¯gsted-Nielsen J., Binderup E, Calverley M.J., Makin H.L.J. and Jones G. (1997) The vitamin D analog, KH1060 is rapidly degraded both in vivo and in vitro via several pathways: principal metabolites generated retain significant biological activity. Endocrinology, 138: 5485-5496.

Jones G, Strugnell S and DeLuca HF (1998) Current understanding of the molecular actions of vitamin D. Physiological Reviews 78:1193-1231.

White J.A., Ramshaw H, Taimi, M Stangle, W, Zhang A, Everingham S, Creighton S, Tam S-P, Jones G and Petkovich M (2000) Identification of the human cytochrome P450, P450RAI-2, which is predominantly expressed in the adult cerebellum and is responsible for all-trans retinoic acid metabolism. Proc Natl Acad Sci USA., in press