Familial clustering and ethnic differences suggest that visceral leishmaniasis caused by Leishmania donovani is under genetic control. A recent genome scan provided evidence for a major susceptibility gene on Chromosome 22q12 in the Aringa ethnic group in Sudan. We now report a genome-wide scan using 69 families with 173 affected relatives from two villages occupied by the related Masalit ethnic group. A primary ten-centimorgan scan followed by refined mapping provided evidence for major loci at 1p22 (LOD score 5.65; nominal p=1.72×10-7; empirical p < 1×10-5; λS= 5.1) and 6q27 (LOD score 3.74; nominal p = 1.68 × 10-5; empirical p < 1 × 10-4; λS = 2.3) that were Y chromosome-lineage and village-specific. Neither village supported a visceral leishmaniasis susceptibility gene on 22q12. The results suggest strong lineage-specific genes due to founder effect and consanguinity in these recently immigrant populations. These chance events in ethnically uniform African populations provide a powerful resource in the search for genes and mechanisms that regulate this complex disease.
Y chromosome lineage- and village-specific genes on chromosomes 1p22 and 6q27 control visceral leishmaniasis in Sudan / E.N. Miller, M. Fadl, H.S. Mohamed, A. Elzein, S.E. Jamieson, H.J. Cordell, C.S. Peacock, M. Fakiola, M. Raju, E.A. Khalil, A. Elhassan, A.M. Musa, M.E. Ibrahim, J.M. Blackwell. - In: PLOS GENETICS. - ISSN 1553-7390. - 3:5(2007 May), pp. e71.679-e71.688. [10.1371/journal.pgen.0030071]
Y chromosome lineage- and village-specific genes on chromosomes 1p22 and 6q27 control visceral leishmaniasis in Sudan
M. Fakiola;
2007
Abstract
Familial clustering and ethnic differences suggest that visceral leishmaniasis caused by Leishmania donovani is under genetic control. A recent genome scan provided evidence for a major susceptibility gene on Chromosome 22q12 in the Aringa ethnic group in Sudan. We now report a genome-wide scan using 69 families with 173 affected relatives from two villages occupied by the related Masalit ethnic group. A primary ten-centimorgan scan followed by refined mapping provided evidence for major loci at 1p22 (LOD score 5.65; nominal p=1.72×10-7; empirical p < 1×10-5; λS= 5.1) and 6q27 (LOD score 3.74; nominal p = 1.68 × 10-5; empirical p < 1 × 10-4; λS = 2.3) that were Y chromosome-lineage and village-specific. Neither village supported a visceral leishmaniasis susceptibility gene on 22q12. The results suggest strong lineage-specific genes due to founder effect and consanguinity in these recently immigrant populations. These chance events in ethnically uniform African populations provide a powerful resource in the search for genes and mechanisms that regulate this complex disease.| File | Dimensione | Formato | |
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