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Searching for signals of evolutionary selection in 168 genes related to immune function
Authors:Emily C. Walsh  Pardis Sabeti  Holli B. Hutcheson  Ben Fry  Stephen F. Schaffner  Paul I. W. de Bakker  Patrick Varilly  Alejandro A. Palma  Jessica Roy  Richard Cooper  Cheryl Winkler  Yi Zeng  Guy de The  Eric S. Lander  Stephen O’Brien  David Altshuler
Affiliation:(1) Novartis Institutes for Biomedical Research, 250 Mass Ave, Cambridge, MA 02139, USA;(2) Broad Institute of MIT and Harvard, 1 Kendall Square, Cambridge, MA 02139, USA;(3) Laboratory of Genomic Diversity, National Cancer Institute, Frederick, MD, USA;(4) Department of Preventive Medicine and Epidemiology, Loyola University Medical School, Maywood, IL, USA;(5) Institute for Viral Disease Control and Prevention, Beijing, China;(6) The Institute Pasteur, Paris, France;(7) Massachusetts General Hospital, Boston, MA, USA;(8) Harvard Medical School, Boston, MA, USA
Abstract:Pathogens have played a substantial role in human evolution, with past infections shaping genetic variation at loci influencing immune function. We selected 168 genes known to be involved in the immune response, genotyped common single nucleotide polymorphisms across each gene in three population samples (CEPH Europeans from Utah, Han Chinese from Guangxi, and Yoruba Nigerians from Southwest Nigeria) and searched for evidence of selection based on four tests for non-neutral evolution: minor allele frequency (MAF), derived allele frequency (DAF), Fst versus heterozygosity and extended haplotype homozygosity (EHH). Six of the 168 genes show some evidence for non-neutral evolution in this initial screen, with two showing similar signals in independent data from the International HapMap Project. These analyses identify two loci involved in immune function that are candidates for having been subject to evolutionary selection, and highlight a number of analytical challenges in searching for selection in genome-wide polymorphism data. Electronic Supplementary Material Supplementary material is available for this article at and is accessible for authorized users. Emily C. Walsh, Pardis Sabeti, Holli B. Hutcheson, and Ben Fry have contributed equally to this work and Stephen O’Brien and David Altshuler have jointly supervised this project
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