Canine Multiple System Degeneration Associated with Sequence Variants in SERAC1

• Published in: Genes 2024-10, Vol.15 (11), p.1378
• Main Authors: Zeng, Rong, Guo, Juyan, Bullock, Garrett, Johnson, Gary S, Katz, Martin L
• Format: Article
• Language: English
• Subjects: Akinesia; Animal euthanasia; Animals; Ataxia; Automation; Brain; Caudate nucleus; Cerebellum; Chromosome 1; Cross-breeding; Degeneration; DNA sequencing; Dog Diseases - genetics; Dogs; Enzymes; Epidemiology; Exons - genetics; Female; Gait; Gene mapping; Genes; Genetic crosses; Genetic testing; Genomes; Genomics; Genotype; Genotype & phenotype; Genotypes; Genotyping; Heterozygotes; Liberalism; Male; Movement disorders; Next-generation sequencing; Nucleotide sequence; Phenotype; Phenotypes; Substantia nigra; Therapeutic applications
• ISSN: 2073-4425; 2073-4425
• DOI: 10.3390/genes15111378

Canine multiple system degeneration (CMSD) is an early onset, progressive movement disorder affecting Kerry Blue Terriers and Chinese Crested dogs. The associated pathologic lesions include degeneration of the cerebellum, caudate nucleus, and substantia nigra. CMSD is inherited as an autosomal recessive trait in both dog breeds. Previous linkage mapping localized the CMSD locus to a 15 MB region on canine chromosome 1 (CFA1). Next-generation sequencing was used to generate whole-genome sequences from the DNA of an affected dog from each breed. The resulting sequence reads were aligned to the NCBI canine reference genome (build 3.1). Among the homozygous sequence variants within the CFA1 target region, a nonsense variant in exon 15 of was identified in the affected Kerry Blue Terrier, while in the Chinese Crested dog, a 4 bp deletion in the exon 4 acceptor splice site was found. RT-PCR showed that this deletion resulted in exon 4 skipping. Genotyping of large cohorts of Kerry Blue Terriers and Chinese Crested dogs for the respective breed-specific variants showed complete concordance between genotype and disease phenotype. Genotype-phenotype concordance was also observed in offspring generated by cross breeding between -heterozygous Kerry Blue Terrier and Chinese Crested dogs, with only the compound heterozygotes exhibiting the disease phenotype, further confirming the recessive inheritance of CMSD. Variants in human are associated with disorders with a range of ages of disease onset and patterns of clinical signs, but that are all characterized by movement abnormalities similar to those of the dogs with CMSD. Canine CMSD could serve as a valuable model to elucidate the mechanisms underlying SERAC1-deficiency disorders and to evaluate potential therapeutic interventions.