A major susceptibility locus for leprosy in India maps to chromosome 10p13

被引:138
作者
Siddiqui, MR
Meisner, S
Tosh, K
Balakrishnan, K
Ghei, S
Fisher, SE
Golding, M
Narayan, NPS
Sitaraman, T
Sengupta, U
Pitchappan, R
Hill, AVS [1 ]
机构
[1] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford, England
[2] Madurai Kamaraj Univ, Madurai 625021, Tamil Nadu, India
[3] JALMA Inst, Agra, Uttar Pradesh, India
[4] Leprosy Project, Sakthi Nagar, India
[5] Hindu Mission Hosp, Kumbakonam, India
关键词
D O I
10.1038/86958
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Leprosy, a chronic infectious disease caused by Mycobacterium leprae, is prevalent in India, where about half of the world's estimated 800,000 cases occur(1). A role for the genetics of the host in variable susceptibility to leprosy has been indicated by familial clustering, twin studies, complex segregation analyses and human leukocyte antigen (HLA) association studies. We report here a genetic linkage scan of the genomes of 224 families from South India, containing 245 independent affected sibpairs with leprosy, mainly of the paucibacillary type. In a two-stage genome screen using 396 microsatellite markers, we found significant linkage (maximum lod score (MLS)=4.09, P<2x10(-5)) on chromosome 10p13 for a series of neighboring microsatellite markers, providing evidence for a major locus for this prevalent infectious disease. Thus, despite the polygenic nature of infectious disease susceptibility, some major, non-HLA-linked loci exist that may be mapped through obtainable numbers of affected sibling pairs.
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页码:439 / 441
页数:3
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