American Kennel Club Canine Health Foundation
Deborah (DD) A. DiLalla, Executive Director
P.O. Box 37941, Raleigh, NC 27627-7941
Phone: 1-888-682-9696 or 919-334-4010
www.akcchf.org 

Batten Disease Support and Research Assoc
Lance Johnston, Executive Director
120 Humphries Dr., Suite 2
Reynoldsburg, OH 43068
Phone: 1-800-448-4570 or 740-927-4298
www.bdsra.org

Martin L. Katz, Ph.D
Professor, Ophthalmology, Genetics, Pathobiology, Molecular Biology
Mason Eye Insititute, University of Missouri School of Medicine
One Hospital Drive, Columbia MO 65212
Phone: 573-882-8480
e-mail: katzm@health.missouri.edu
 

Canine Neuronal Ceroid Lipofuscinosis website

COLUMBIA, Mo – Dogs are more than just man’s best friend; at the University of Missouri-Columbia, dogs are helping with life-saving research. Tibetan Terriers are contributing to an extensive canine DNA bank in an on-going research program studying the genetic bases of diseases that affect both dogs and humans. The Tibetan Terriers can be stricken with a neurological disease, known as neuronal ceroid lipofuscinosis (NCL), which has a human equivalent called Batten disease.

NCL diseases are inherited neurological disorders that have no cure. Though rare, children of parents who are carriers each have a one in four chance of inheriting the terminal disease. In order to better understand the pathology of the disease and develop therapies, Martin Katz, professor of ophthalmology with dual appointments in the School of Medicine and the College of Veterinary Medicine, is looking to the Tibetan Terriers for help.

“The purebred dog population provides an ideal model for genetic research,” said Wayne Ferguson, president of the American Kennel Club Canine Health Foundation. “The dogs’ pedigrees provide detailed multigenerational relationship information. The shorter lifespan of a dog allows researchers to compress studies that would take much longer with people.”

Katz is searching for the genetic bases of the disease by studying the large pool of DNA provided by the dogs’ owners. The normal canine genome, which has been sequenced, is compared to the DNA of the affected and unaffected Tibetan Terriers to pinpoint the NCL mutation in this breed. Katz said in order for genetic mapping to be successful, information about the disease status of the dogs and their pedigrees must be accurate. Because of the excellent record-keeping by breed registries and close observations of their dogs by owners, registered purebred dogs are ideal subjects for genetic studies.

Using the “candidate gene” approach, Katz sequenced, or identified, the genes of affected Tibetan Terriers in specific areas thought to be comparable to those where human markers associated with the condition have been identified. Using this approach, he was able to eliminate mutations in known NCL genes as the cause of the Tibetan Terrier disease.

The next step is the identification of the NCL mutation in Tibetan Terriers. This now requires that the mutant gene be located through a process called mapping or linkage analysis. This analysis involves detailed comparison of the DNA from a large number of affected dogs with the DNA of their parents and affected littermates.

"The organization of genes in a genome is like the organization of books in a library,” Katz said. “Genes are arranged in a specific order on a number of different chromosomes, much like books are placed in specific orders on specific shelves in a library. Determining the precise location of a disease-causing mutation within the genome will identify the disease gene, just as going to a specific location on a specific shelf in a library will result in a particular book being located.”

Once the NCL mutation in Tibetan Terriers has been identified, a simple test for the mutation can be performed on any dog using DNA extracted from a blood sample. This will enable breeders to screen dogs prior to breeding to prevent generating affected dogs in the future. Identification of the Tibetan Terrier NCL mutation also will make it possible to determine whether any humans with NCL have the mutations in the corresponding human gene.

According to Katz, human NCL often goes misdiagnosed because the disease is rare and early symptoms overlap those of other disorders. Eventually, affected children develop an array of symptoms that include blindness, seizures, cognitive decline and loss of motor function. Often, it is not until these symptoms are well advanced that a correct diagnosis is made. Research currently is underway to develop gene and stem cell therapies for the NCL diseases, but to be effective any therapy will have to begin early in the course of the disease. Identifying the NCL mutations will enable definitive diagnoses of these diseases to be made on the basis of DNA tests early enough to make therapeutic interventions effective.

“Dr. Katz’s work with Tibetan Terriers has the potential to fast forward the entire research process.” said Lance Johnson, executive director of the Batten Disease Research and Support Association. “As we are increasingly able to correlate canine research efforts with human studies, we expect the crossover opportunities to be phenomenal.”

The Tibetan Terrier DNA bank was originally conceived and developed by Stuart Eckmann and Linda Bell, who oversee the Tibetan Terrier Club of America’s health programs. In a collaborative effort with MU, Eckmann refers owners of affected dogs to Katz for examination of retinal and neural tissue. The result of this effort has been a more complete description of the condition than exists in any current textbook. Using Eckmann’s model, MU has expanded canine DNA banking for genetic studies to many other dog breeds and diseases including epilepsy, cancer and Parkinson’s disease.

Support for Katz’s work has been provided by the American Kennel Club Canine Health Foundation, the Batten Disease Support and Research Association, and Research to Prevent Blindness, Inc. Eckmann, Johnston, and Katz presented their collaboration at the 2005 National Parent Club Canine Health Conference held in St Louis, MO, October 21, through October 23, 2005.