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Polymorphisms in MC3R Promoter and CTSZ 3'UTR Are Associated with Tuberculosis Susceptibility

Overview
Journal Eur J Hum Genet
Specialty Genetics
Date 2011 Mar 4
PMID 21368909
Citations 19
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Abstract

We have validated the association of two genes on chromosome 20q13.31-33 with tuberculosis susceptibility. A previous genome-wide linkage study performed by Cooke et al identified the genes melanocortin-3-receptor (MC3R) and cathepsin Z (CTSZ) as possible candidates in tuberculosis susceptibility. MC3R has been implicated in obesity studies and is known to play a role in many biological systems including the regulation of energy homeostasis and fat metabolism. CTSZ has been detected in immune cells, such as macrophages and monocytes, and it is hypothesized that the protein may play a role in the immune response. In our South African population a case-control study confirmed the previously reported association with a single-nucleotide polymorphism (SNP) in CTSZ and found an association in MC3R with a SNP not previously implicated in tuberculosis susceptibility. Six SNPs in MC3R and eight in CTSZ were genotyped and haplotypes were inferred. SNP rs6127698 in the promoter region of MC3R (cases = 498; controls = 506) and rs34069356 in the 3'UTR of CTSZ (cases = 396; controls = 298) both showed significant association with tuberculosis susceptibility (P = 0.0004 and < 0.0001, respectively), indicating that pathways involving these proteins, not previously researched in this disease, could yield novel therapies for tuberculosis.

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References
1.
Rached M, Buronfosse A, Begeot M, Penhoat A . Inactivation and intracellular retention of the human I183N mutated melanocortin 3 receptor associated with obesity. Biochim Biophys Acta. 2004; 1689(3):229-34. DOI: 10.1016/j.bbadis.2004.03.009. View

2.
Chen A, Marsh D, Trumbauer M, Frazier E, Guan X, Yu H . Inactivation of the mouse melanocortin-3 receptor results in increased fat mass and reduced lean body mass. Nat Genet. 2000; 26(1):97-102. DOI: 10.1038/79254. View

3.
Tosh K, Meisner S, Siddiqui M, Balakrishnan K, Ghei S, Golding M . A region of chromosome 20 is linked to leprosy susceptibility in a South Indian population. J Infect Dis. 2002; 186(8):1190-3. DOI: 10.1086/343806. View

4.
Lee E, Lee S, Jung J, Lee W, Kim B, Park K . Differential regulation of cAMP-mediated gene transcription and ligand selectivity by MC3R and MC4R melanocortin receptors. Eur J Biochem. 2001; 268(3):582-91. DOI: 10.1046/j.1432-1327.2001.01900.x. View

5.
Bellamy R, Beyers N, McAdam K, Ruwende C, Gie R, Samaai P . Genetic susceptibility to tuberculosis in Africans: a genome-wide scan. Proc Natl Acad Sci U S A. 2000; 97(14):8005-9. PMC: 16660. DOI: 10.1073/pnas.140201897. View