Peer-reviewed veterinary case report
Australian Cattle Dogs have fatal brain disease from CLN5 gene
By Kolicheski, A et al.·Published in Journal of veterinary internal medicine·2016·Department of Veterinary Pathobiology·View original on PubMed →
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Original publication title: Australian Cattle Dogs with Neuronal Ceroid Lipofuscinosis are Homozygous for a CLN5 Nonsense Mutation Previously Identified in Border Collies.
- Species:
- dog
Plain-English summary
A young adult Australian Cattle Dog was diagnosed with neuronal ceroid lipofuscinosis (NCL), a serious neurodegenerative disease. Researchers found a specific genetic mutation (CLN5:c.619C>T) that is likely responsible for this condition, which causes harmful substances to build up in the dog's brain. This mutation was also previously identified in Border Collies with a similar disease. Knowing the genetic cause can help veterinarians confirm NCL in affected dogs through DNA testing, which may aid in managing the condition. Unfortunately, NCL is a progressive disease with no cure.
People also search for: Australian Cattle Dog NCL symptoms · dog genetic testing for NCL · what is neuronal ceroid lipofuscinosis in dogs
Abstract
BACKGROUND: Neuronal ceroid lipofuscinosis (NCL), a fatal neurodegenerative disease, has been diagnosed in young adult Australian Cattle Dogs. OBJECTIVE: Characterize the Australian Cattle Dog form of NCL and determine its molecular genetic cause. ANIMALS: Tissues from 4 Australian Cattle Dogs with NCL-like signs and buccal swabs from both parents of a fifth affected breed member. Archived DNA samples from 712 individual dogs were genotyped. METHODS: Tissues were examined by fluorescence, electron, and immunohistochemical microscopy. A whole-genome sequence was generated for 1 affected dog. A TaqMan allelic discrimination assay was used for genotyping. RESULTS: The accumulation of autofluorescent cytoplasmic storage material with characteristic ultrastructure in tissues from the 4 affected dogs supported a diagnosis of NCL. The whole-genome sequence contained a homozygous nonsense mutation: CLN5:c.619C>T. All 4 DNA samples from clinically affected dogs tested homozygous for the variant allele. Both parents of the fifth affected dog were heterozygotes. Archived DNA samples from 346 Australian Cattle Dogs, 188 Border Collies, and 177 dogs of other breeds were homozygous for the reference allele. One archived Australian Cattle Dog sample was from a heterozygote. CONCLUSIONS AND CLINICAL IMPORTANCE: The homozygous CLN5 nonsense is almost certainly causal because the same mutation previously had been reported to cause a similar form of NCL in Border Collies. Identification of the molecular genetic cause of Australian Cattle Dog NCL will allow the use of DNA tests to confirm the diagnosis of NCL in this breed.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/27203721/