TY - JOUR
T1 - Genetic Structure of Susceptibility Traits for Hip Dysplasia and Microsatellite Informativeness of an Outcrossed Canine Pedigree
AU - Todhunter, Rory J.
AU - Bliss, S. P.
AU - Casella, G.
AU - Wu, R.
AU - Lust, G.
AU - Burton-Wurster, N. I.
AU - Williams, A. J.
AU - Gilbert, R. O.
AU - Acland, G. M.
N1 - Funding Information:
From the Department of Clinical Sciences (Todhunter, Bliss, and Gilbert) and the James A. Baker Institute for Animal Health (Acland, Lust, and Williams), College of Veterinary Medicine, Cornell University, Ithaca, NY, and the Department of Statistics, University of Florida, Gainesville, FL (Wu and Casella). This work was supported by the Cornell University College of Veterinary Medicine Unrestricted Alumni Fund and Consolidated Grants Program; the Gussy Gruver, Van Sloun, and Morris Animal Foundations; Nestlé Purina; and National Institutes of Health grants RO1 AR35664 and RO1 AR47558. The authors thank Catherine Mellersh for providing the Excel spreadsheet format for PIC determination and Victoria Rininger, Carol Bayles, and Elizabeth Corey for excellent technical assistance. This paper was delivered at the Advances in Canine and Feline Genomics symposium, St. Louis, MO, May 16–19, 2002.
PY - 2003/1
Y1 - 2003/1
N2 - An outcrossed canine pedigree was developed for quantitative trait locus (QTL) mapping of hip dysplasia by breeding dysplastic Labrador retrievers to trait-free greyhounds. Measured susceptibility traits included age at onset of femoral capital chondroepiphyseal ossification (OSS), maximum hip distraction (laxity) index (DI), and the dorsolateral subluxation (DLS) score. The pedigrees consisted of 147 dogs representing four generations. For 59 dogs genotyped with 65 microsatellites, the median heterozygosity and polymorphic information content (PIC) values of the F1 generation were 0.82 and 0.68, respectively. Seventy-seven percent of microsatellites had a PIC greater than 0.59 in the F1s. Ninety-six percent of alleles showed Mendelian inheritance. Based on marker informativeness, approximately 350 randomly selected markers would be required for genome-wide screening to obtain an average interval between informative markers of 10 cM. Heritability was estimated as 0.43, 0.5, and 0.61 for OSS, DI, and the DLS score, respectively. Biometric estimates of the mean (± variance) effective number of segregating QTLs was 1.2 (± 0.05), 0.8 (± 0.02), and 1.0 (± 0.03) for OSS, DI, and the DLS score, respectively. The distributions of simulated backcross trait data suggested that the loci controlling these traits acted additively and that the DI may be controlled by a major locus. When combined with previous power and quantitative genetic analyses, these estimates indicate that this pedigree is informative for QTL mapping of hip dysplasia traits.
AB - An outcrossed canine pedigree was developed for quantitative trait locus (QTL) mapping of hip dysplasia by breeding dysplastic Labrador retrievers to trait-free greyhounds. Measured susceptibility traits included age at onset of femoral capital chondroepiphyseal ossification (OSS), maximum hip distraction (laxity) index (DI), and the dorsolateral subluxation (DLS) score. The pedigrees consisted of 147 dogs representing four generations. For 59 dogs genotyped with 65 microsatellites, the median heterozygosity and polymorphic information content (PIC) values of the F1 generation were 0.82 and 0.68, respectively. Seventy-seven percent of microsatellites had a PIC greater than 0.59 in the F1s. Ninety-six percent of alleles showed Mendelian inheritance. Based on marker informativeness, approximately 350 randomly selected markers would be required for genome-wide screening to obtain an average interval between informative markers of 10 cM. Heritability was estimated as 0.43, 0.5, and 0.61 for OSS, DI, and the DLS score, respectively. Biometric estimates of the mean (± variance) effective number of segregating QTLs was 1.2 (± 0.05), 0.8 (± 0.02), and 1.0 (± 0.03) for OSS, DI, and the DLS score, respectively. The distributions of simulated backcross trait data suggested that the loci controlling these traits acted additively and that the DI may be controlled by a major locus. When combined with previous power and quantitative genetic analyses, these estimates indicate that this pedigree is informative for QTL mapping of hip dysplasia traits.
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U2 - 10.1093/jhered/esg006
DO - 10.1093/jhered/esg006
M3 - Article
C2 - 12692161
AN - SCOPUS:0037558452
SN - 0022-1503
VL - 94
SP - 39
EP - 48
JO - Journal of Heredity
JF - Journal of Heredity
IS - 1
ER -