Genes Associated with SLE Are Targets of Recent Positive Selection

Author:

Ramos Paula S.1,Shaftman Stephanie R.2,Ward Ralph C.2,Langefeld Carl D.3

Affiliation:

1. Department of Medicine, Medical University of South Carolina, Charleston, SC 29425, USA

2. Department of Public Health Sciences, Medical University of South Carolina, Charleston, SC 29425, USA

3. Department of Public Health Sciences, Wake Forest School of Medicine and Center for Public Health Genomics, Winston-Salem, NC 27157, USA

Abstract

The reasons for the ethnic disparities in the prevalence of systemic lupus erythematosus (SLE) and the relative high frequency of SLE risk alleles in the population are not fully understood. Population genetic factors such as natural selection alter allele frequencies over generations and may help explain the persistence of such common risk variants in the population and the differential risk of SLE. In order to better understand the genetic basis of SLE that might be due to natural selection, a total of 74 genomic regions with compelling evidence for association with SLE were tested for evidence of recent positive selection in the HapMap and HGDP populations, using population differentiation, allele frequency, and haplotype-based tests. Consistent signs of positive selection across different studies and statistical methods were observed at several SLE-associated loci, includingPTPN22,TNFSF4,TET3-DGUOK,TNIP1,UHRF1BP1,BLK, andITGAMgenes. This study is the first to evaluate and report that several SLE-associated regions show signs of positive natural selection. These results provide corroborating evidence in support of recent positive selection as one mechanism underlying the elevated population frequency of SLE risk loci and supports future research that integrates signals of natural selection to help identify functional SLE risk alleles.

Funder

National Institutes of Health

Publisher

Hindawi Limited

Subject

Immunology and Microbiology (miscellaneous),Immunology,Immunology and Allergy

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