Cornell researchers have completed the largest genetic study of dogs to date, comprising the genetic analysis of 4,200 dogs.
The study investigated 180,000 genetic markers, DNA sequences with a known physical location on a chromosome. Such markers can help link an inherited disease with the responsible gene.
The study, published in the journal Nature Communications, is a big step toward efficiently mapping genes responsible for complex diseases in dogs, most of which are very similar in humans, thereby accelerating our understanding of human genetic diseases. By identifying important genes and proteins in dogs for diseases and traits, researchers may then test those homologous genes in humans.
There is increased interest in dogs as a model for studying human diseases because dogs share more than 350 diseases with humans – from hip dysplasia to lymphoma – and similar pathways and genes often underlie these shared diseases, according to the paper.
“The more we know about the genetic basis of diseases, the better we are at keeping pure-bred dog populations genetically healthy,” said Adam Boyko, assistant professor of biomedical sciences at Cornell’s College of Veterinary Medicine and the paper’s senior author. Jessica Hayward, a postdoctoral research associate in Boyko’s lab, and Marta Castelhano, director of the Cornell Veterinary Biobank, are co-lead authors of the paper.
But genetics in dogs is far simpler than in humans, and since dogs are diagnosed with many of the same diseases as humans, studying dog genetics is a “useful and underused way to understand genetic diseases from a human perspective,” Boyko said. For complex diseases, the researchers identified areas on the genome that are associated with hip dysplasia, elbow dysplasia, idiopathic epilepsy, lymphoma, mast cell tumor and granulomatous colitis. The researchers also identified genes that influence such traits as body size, fur length and shedding.
“We found 17 genes for body size in dogs, and by looking at those genes we can predict a dog’s size with 90 percent accuracy,” said Boyko. He added that identifying such genes is much easier in dogs than in humans, where hundreds of genes contribute to body size.
Human disease-mapping studies generally include genotyping tens of thousands of individuals and looking at 1 million markers across the genome. In this study, the researchers conducted simulations to show that “in dogs, we expect to be able to identify genetic risk factors for most major diseases with 1000 individual dogs and 1000 controls,” Boyko said.
The study was made possible due to samples of more than 150 breeds, 170 mixed-breed dogs and 350 free-ranging village dogs from the Cornell Veterinary Biobank; the project represents the culmination of several years of work by the biobank to collect samples and secure funding.
Source: Cornell University