Skip to main content
Premium Trial:

Request an Annual Quote

$17M EU Project to Study Dog Genomes to Gain Insight into Human Disease

NEW YORK (GenomeWeb News) — The European Commission has awarded €12 million ($16.9 million) to a consortium of European research centers through 2012 to conduct genome-wide association studies on several dog breeds in hopes of gaining a better understanding of human diseases.
 
The program, called Lupa, is funded under the EC’s Seventh Framework Program. It involves 20 veterinary schools in 12 European nations that will collect 10,000 DNA samples from purebred dog species that have genetic diseases and from healthy dogs.
 
The researchers will compare the genomes of healthy and diseased dogs within single breeds to identify SNPs that could help target genes responsible for any of 18 different diseases, including cancer and heart disease, inflammatory disorders, and neurological disorders.
 
“We have decided to focus on certain areas and to standardize the characterization of these diseases,” Uppsala University Professor Leif Andersson said in a statement from the EC.
 
Some of the breeds involved in the project include the Golden Retriever and German Shepherd for cancer studies, the English Cocker Spaniel for aggressive behavior, the Doberman and Boxer for hypothyroid diseases, Great Danes and Irish Wolfhounds for cardiovascular disorders, and the Greyhound and Collie as part of a monogenic disorders package.

The Scan

Sick Newborns Selected for WGS With Automated Pipeline

Researchers successfully prioritized infants with potential Mendelian conditions for whole-genome sequencing or rapid whole-genome sequencing, as they report in Genome Medicine.

Acne-Linked Loci Found Through GWAS Meta-Analysis

Researchers in the European Journal of Human Genetics find new and known acne vulgaris risk loci with a genome-wide association study and meta-analysis, highlighting hair follicle- and metabolic disease-related genes.

Retina Cell Loss Reversed by Prime Editing in Mouse Model of Retinitis Pigmentosa

A team from China turns to prime editing to correct a retinitis pigmentosa-causing mutation in the PDE6b gene in a mouse model of the progressive photoreceptor loss condition in the Journal of Experimental Medicine.

CRISPR Screens Reveal Heart Attack-Linked Gene

Researchers in PLOS Genetics have used CRISPR screens to home in on variants associated with coronary artery disease that affect vascular endothelial function.