Lupus susceptibility loci in New Zealand mice.

D H Kono(Scripps Research Institute), Rufus W. Burlingame(Scripps Research Institute), D. G. Cunningham Owens(Scripps Research Institute), Akira Kuramochi(Scripps Research Institute), Robert Balderas(Scripps Research Institute), Dimitrios Balomenos(Scripps Research Institute), A N Theofilopoulos(Scripps Research Institute)
Proceedings of the National Academy of Sciences
October 11, 1994
Cited by 344Open Access
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Abstract

Susceptibility to systemic lupus erythematosus has been unequivocally established to be an inherited trait, but the exact genes and how they confer susceptibility remain largely unknown. In this study of (NZB x NZW)F2 intercross mice, we used linkage analysis of markers covering > 90% of the autosomal genome and identified eight susceptibility loci (Lbw1 to -8, chromosomes 17, 4-7, 18, 1, 11, respectively) associated with antichromatin autoantibody production, glomerulonephritis, and/or mortality. Only one locus, the major histocompatibility complex, was linked to all three traits. Two other loci were associated with both glomerulonephritis and mortality, whereas the remaining loci were linked to one of the above traits. Two additional loci (Sbw1 and -2) that contributed to splenomegaly were also identified. The Sbw2 locus mapped to the identical region as Lbw2, a locus on chromosome 4 linked to glomerulonephritis and mortality, suggesting a single locus with pleiotropic effects. The results indicate that the immunopathologic features of lupus are affected by distinct, but additive, genetic contributions. Studies to determine the nature of the genes associated with these loci should help define the genetic mechanisms involved in this systemic autoimmune disease.


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