Dog Genome Sequence and Analysis Published in NaturePublished On: Wed, Dec 7th, 2005 | Bioinformatics | By BioNews
An international research team led by scientists at the Broad Institute of MIT and Harvard announced today the completion of a high-quality genome sequence of the domestic dog, together with a catalog of 2.5 million specific genetic differences across several dog breeds. Published in the December 8 issue of Nature, the dog research sheds light on both the genetic similarities between dogs and humans and the genetic differences between dog breeds. Comparison of the dog and human DNA reveals key secrets about the regulation of the master genes that control embryonic development. Comparison among dogs also reveals the structure of genetic variation among breeds, which can now be used to unlock the basis of physical and behavioral differences, as well the genetic underpinnings of diseases common to domestic dogs and their human companions.
â€œOf the more than 5,500 mammals living today, dogs are arguably the most remarkable,â€ said senior author Eric Lander, director of the Broad Institute, professor of biology at MIT and systems biology at Harvard Medical School, and a member of the Whitehead Institute for Biomedical Research. â€œThe incredible physical and behavioral diversity of dogs — from Chihuahuas to Great Danes â€“ is encoded in their genomes. It can uniquely help us understand embryonic development, neurobiology, human disease and the basis of evolution.â€
Similarities to humans
Dogs not only occupy a special place in human hearts, they also sit at a key branch point in the evolutionary tree relative to humans. By tracking evolutionâ€™s genetic footprints through the dog, human and mouse genomes, the scientists found that humans share more of their ancestral DNA with dogs than with mice, confirming the utility of dog genetics for understanding human disease.
Most importantly, the comparison revealed the regions of the human genome that are most highly preserved across mammals. Roughly 5% of the human genome has been well preserved by evolution over the past 100 million years and must encode important biological functions. The researchers discovered that the most highly conserved of these sequences are not randomly distributed throughout the genome. Instead, they are crowded around just a tiny fraction (about 1%) of the genes that encode crucial regulatory proteins involved in development (such as transcription factors or axon guidance receptors). â€œThe clustering of regulatory sequences is incredibly interesting,â€ said Kerstin Lindblad-Toh, first author of the Nature paper and co-director of the genome sequencing and analysis program at Broad. â€œIt means that a small subset of crucial human genes is under much more elaborate control than we had ever imagined.â€
Differences between dog breeds
Dogs were domesticated from gray wolves as long as 100,000 years ago, but selective breeding over the past few centuries has made modern dog breeds a testament to biological diversity. Obvious examples include the contrasting body sizes of 6-pound Chihuahuas and 120-pound Great Danes, the hyperactivity of Jack Russell terriers relative to mild-mannered basset hounds, and the herding instincts of Shetland sheepdogs compared with the protective proclivity of dalmatians.
Efforts to create the genetic tools needed to map important genes in dogs have gained momentum over the last 15 years, and already include a partial survey of the poodle genome. More than two years ago, Lindblad-Toh, Lander, and their colleagues embarked on a two-part project to assemble a complete map of the dog genome. First, they acquired high-quality DNA sequence from a female boxer named â€œTasha,â€ covering nearly 99% of the dogâ€™s genome. Using this information as a genetic â€˜compass,â€™ they then sampled the genomes of 10 different dog breeds and other related canine species, including the gray wolf and coyote. By comparing these dogs, they pinpointed ~2.5 million individual genetic differences among breeds, called single nucleotide polymorphisms (SNPs), which serve as recognizable signposts that can be used to locate the genetic contributions to physical and behavioral traits, as well as disease.
Finally, the scientists used the SNP map to reconstruct how intense dog breeding has shaped the genome. They discovered that selective breeding carried large genomic regions of several million bases of DNA into breeds, creating â€˜haplotype blocksâ€™ that are ~100 times larger than seen in the human population. â€œThe huge genomic regions should make it much easier to find the genes responsible for differences in body size, behavior and disease,â€ said Lander. â€œSuch studies will need many fewer markers than for human studies. It should be like hitting the side of a barn.â€
Mapping human disease-related genes in dogs
Breeding programs not only selected for desired traits, they also had the unintended consequence of predisposing many dog breeds to genetic diseases, including heart disease, cancer, blindness, cataracts, epilepsy, hip dysplasia and deafness. With the dog genome sequence and the SNP map, scientists around the world now have the tools to identify these disease genes.
Humans suffer from many of the same illnesses as their four-legged friends and even show similar symptoms, but the genetic underpinnings have proved difficult to trace. â€œThe genetic contributions to many common diseases appear to be easier to uncover in dogs,â€ said Lindblad-Toh. â€œIf so, it is a significant step forward in understanding the roots of genetic disease in both dogs and humans.â€
For this work, the dog-owner community is an essential collaborator. â€œWe deeply appreciate the generous cooperation of individual dog owners and breeders, breed clubs and veterinary schools in providing blood samples for genetic analysis and disease gene mapping,â€ said Lindblad-Toh. â€œWithout their interest and help we could not be doing this work.â€
Kerstin Lindblad-Toh et al. Genome sequence, comparative analysis and haplotype structure of the domestic dog (2005) Nature , Volume 438 Number 7069 pp711-888