Date Available

6-17-2014

Year of Publication

2014

Document Type

Doctoral Dissertation

Degree Name

Doctor of Philosophy (PhD)

College

Agriculture, Food and Environment

Department/School/Program

Veterinary Science

Advisor

Dr. Ernest Bailey

Abstract

Champagne dilution of coat color in horses is caused by dominant gene action. Three sire families were identified as segregating for this trait. Genome wide linkage analysis using 104 microsatellite DNA markers was used to map the gene to ECA14 (LOD > 11.0). Four genes, namely SPARC, SLC36A1, SLC36A2 and SLC36A3, were selected from the region implicated by linkage and their exons sequenced. DNA sequences were compared for two homozygotes for Champagne dilution, two heterozygotes and two horses without dilution. A single base change in exon 2 of SLC36A1 was found unique to horses exhibiting Champagne dilution. This change in base 188 of the cDNA from a C to a G (Genbank REFSEQ: Non-champagne EU432176 and Champagne EU432177), is predicted to cause an amino acid change from threonine to arginine in the first transmembrane region. No exceptions to the association of this mutation with the Champagne dilution (CH) allele were identified based on testing 182 additional horses representing 15 breeds, suggesting that this mutation may be the causative for the dilution phenotype. This is the first evidence for a phenotypic effect of mutation of the gene. Identifying this variant also gives breeders a new tool for selecting breeding stock.

Extreme lordosis is a condition in which the dorsal to ventral curvature of the back is accentuated. The condition is considered a conformation fault by many Saddlebred breeders and is commonly referred to as swayback, softback or lowback. Previous studies suggested the existence of a hereditary component in American Saddlebred horses. A whole genome association study was performed utilizing the Illumina SNP50 beadchip containing over 59,000 SNPs. A 3 Mb region on ECA20 was found associated with extreme lordosis. The distribution of markers indicated that the trait had a simple Mendelian recessive mode of inheritance. Subsequently, the association was confirmed and the region was narrowed to just over 500 kb by a higher density SNP assay using 47 SNPs selected from the equine SNP database. Identification of this associated region will allow future studies a better opportunity to locate the mutation responsible for the lordotic phenotype in young American Saddlebred Horses.

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