Open AccessQuantitative trait locus linkage analysis in a large Amish pedigree identifies novel candidate loci for erythrocyte traits
Author(s) -
Hinckley Jesse D.,
Abbott Diana,
Burns Trudy L.,
Heiman Meadow,
Shapiro Amy D.,
Wang Kai,
Paola Jorge Di
Publication year - 2013
Publication title -
molecular genetics and genomic medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.765
H-Index - 29
ISSN - 2324-9269
DOI - 10.1002/mgg3.16
Subject(s) - quantitative trait locus , mean corpuscular hemoglobin concentration , mean corpuscular hemoglobin , genetics , red blood cell distribution width , genetic linkage , locus (genetics) , mean corpuscular volume , biology , hereditary hemochromatosis , candidate gene , heritability , hematocrit , medicine , hemochromatosis , gene , endocrinology
We characterized a large Amish pedigree and, in 384 pedigree members, analyzed the genetic variance components with covariate screen as well as genome‐wide quantitative trait locus ( QTL ) linkage analysis of red blood cell count ( RBC ), hemoglobin ( HB ), hematocrit ( HCT ), mean corpuscular volume ( MCV ), mean corpuscular hemoglobin ( MCH ), mean corpuscular hemoglobin concentration ( MCHC ), red cell distribution width ( RDW ), platelet count ( PLT ), and white blood cell count ( WBC ) using SOLAR . Age and gender were found to be significant covariates in many CBC traits. We obtained significant heritability estimates for RBC , MCV , MCH , MCHC , RDW , PLT , and WBC . We report four candidate loci with Logarithm of the odds (LOD) scores above 2.0: 6q25 ( MCH ), 9q33 ( WBC ), 10p12 ( RDW ), and 20q13 ( MCV ). We also report eleven candidate loci with LOD scores between 1.5 and <2.0. Bivariate linkage analysis of MCV and MCH on chromosome 20 resulted in a higher maximum LOD score of 3.14. Linkage signals on chromosomes 4q28, 6p22, 6q25, and 20q13 are concomitant with previously reported QTL . All other linkage signals reported herein represent novel evidence of candidate QTL . Interestingly rs1800562, the most common causal variant of hereditary hemochromatosis in HFE (6p22) was associated with MCH and MCHC in this family. Linkage studies like the one presented here will allow investigators to focus the search for rare variants amidst the noise encountered in the large amounts of data generated by whole‐genome sequencing.