Genetic factors are estimated to play a role in the development of epilepsy in as many as 40% of epilepsy patients. Several genes affecting the development of symptomatic epilepsies have already been identified, but the genetic background of multifactorial idiopathic epilepsies often remain unknown. Both focal and generalized idiopathic epilepsies occur in Belgian Shepherds. The research group of Professor Hannes Lohi, working in collaboration with Danish, Swedish and American researchers in an EU-funded project, has made a major breakthrough by identifying a chromosome region associated with the most common form of epilepsy in dogs. By comparing the genome of dogs with epilepsy and healthy control dogs a gene region in chromosome 37 was discovered, which if homozygous, increases the risk of epilepsy seven-fold. In addition the research findings indicate that other, still unknown, genetic risk factors may be present in the breed. The identified region has excellent neurological candidate genes for epilepsy and ongoing follow-up research is aimed to identify the specific gene causing epilepsy. Epilepsy genes have not previously been identified in this chromosome region, so the discovery will reveal an entirely new epilepsy gene in dogs and possibly also in humans. The type of epilepsy occurring in Belgian Shepherds is extremely common in also other breeds and thus the discovery may have an impact on the understanding of the epilepsies in different dog breeds.
"There are only few genes in the identified region and I believe that the ongoing analyses will help us to discover the specific epilepsy gene," says Professor Hannes Lohi who led the research. "This would give us a better understanding of the disease mechanisms and provide us with new diagnostic tools for the disease." The Research group of Hannes Lohi has begun an extensive gene-sequencing project in which the entire identified chromosome region will be 'read through' with a next-generation sequencing method. By identifying the specific gene mutation an individual's epilepsy risk could be assessed, although the gene mutation may also be common in dogs that never become symptomatic of epilepsy. "The identified genomic region is likely to be the strongest single risk factor for epilepsy in Belgian Shepherds, and we are studying an interesting gene variant causing an amino acid change in the protein level. However, this homozygous amino acid change is also present in one fifth of healthy Belgian Shepherds. The research continues in the breed and aims to identify the specific mutation for genetic testing in this loci and possible in other chromosomes. The need for the gene test is urgent since as much as 20% of the dogs in this breed are estimated to have epilepsy," comments the first author of the article Eija Seppälä, PhD.
The age of onset of idiopathic epilepsy in Belgian Shepherds is on average 3 years, although the range varies greatly. A seizure often begins as a focal seizure, and the owner may observe abnormal movement, usually on only one side of the dog's body. At this point the dog often seeks out the owner, drools or vomits. With most Belgian Shepherds the seizure becomes generalized and is accompanied with loss of consciousness and irregular cramping in the limbs. The dog may also urinate or defecate involuntarily. Epilepsy is the most common disorder of the nervous system in dogs and different types of genetic epilepsies occur in dozens of dog breeds. The research group has previously identified the first epilepsy gene for symptomatic epilepsy, EPM2B, in Miniature Wirehaired Dachshunds, as well as more recently a gene, LGI2, associated with transient idiopathic epilepsy in Lagotto Romagnolos. The group has also participated in the discovery of a gene for symptomatic epilepsy in Tibetan Terriers. Lohi and his research group have built a canine DNA bank in Finland, which currently holds almost 40 000 samples from more than 250 different breeds. The DNA bank has played a major role in the execution of among others the current research published in March, 2012.
April 17, 2012
Original web page at Science Daily