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donderdag 8 maart 2012

Vitamin D receptor gene methylation is associated with disease susceptibility

Could it be a coincidence I had tuberculosis as a child and then developed lupus as a teenager, ME as years went by and now arthritis?
What if dysfunctional methylation leads to disease?

http://www.ncbi.nlm.nih.gov/pubmed/21168462

Hum Immunol. 2011 Mar;72(3):262-8. Epub 2010 Dec 16.

Vitamin D receptor gene methylation is associated with ethnicity, tuberculosis, and TaqI polymorphism.

Andraos C, Koorsen G, Knight JC, Bornman L.

Department of Biochemistry, University of Johannesburg, Auckland Park, South Africa.


Abstract

The Vitamin D receptor (VDR) gene encodes a transcription factor which, on activation by vitamin D, modulates diverse biologic processes, including calcium homeostasis and immune function. Genetic variation involving VDR shows striking differences in allele frequency between populations and has been associated with disease susceptibility, including tuberculosis and autoimmunity, although results have often been conflicting.
We hypothesized that methylation of VDR may be population specific and that the combination of differential methylation and genetic variation may characterize tuberculosis (TB) predisposition. We use bisulfite conversion and/or pyrosequencing to analyze the methylation status of 17 CpGs of VDR and to genotype 7 SNPs in the 3' CpG Island (CpG island [CGI] 1060), including the commonly studied SNPs ApaI (rs7975232) and TaqI (rs731236).
We show that, for lymphoblastoid cell lines from two ethnically diverse populations (Yoruba from HapMap, n = 30 and Caucasians, n = 30) together with TB cases (n = 32) and controls (n = 29) from the Venda population of South Africa, there are methylation variable positions in the 3' end that significantly distinguish ethnicity (9/17 CpGs) and TB status (3/17 CpGs).
Moreover, methylation status shows complex association with TaqI genotype highlighting the need to consider both genetic and epigenetic variants in genetic studies of VDR association with disease.

Copyright © 2011 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.

Source: http://www.ncbi.nlm.nih.gov/pubmed/21168462