Exonisation of an intronic L1 element in the dystrophin gene associated with X-linked muscular dystrophy in a Border Collie dog.
Mario Van PouckeLiesbet LedeganckLing T GuoG Diane SheltonSofie F M BhattiIne CornelisLuc PeelmanPublished in: Animal genetics (2024)
X-linked recessive dystrophinopathies are the most common muscular dystrophies (MDs) in humans and dogs. To date, 20 breed-specific MD-associated variants are described in the canine dystrophin gene (DMD), including one associated with dystrophin-deficient MD in the Border Collie mixed breed. Here, we report the diagnosis and follow-up of mild dystrophin-deficient MD in a 5-month-old male Border Collie, associated with a novel DMD variant. Diagnosis was based on neurological examination and laboratory evaluations including creatine kinase activity, electromyography and muscle biopsies with immunofluorescent staining. Inspection of the Sashimi plots of the RNA-seq data from the affected muscle biopsy led to the discovery of a 162-bp L1 pseudoexon in DMD intron 63, introducing a frameshift and a premature stop codon (NM_001003343.1: c.9271_9272insN[162] p.(Ala3091fs*21)). Reduced DMD mRNA levels were detected for both the non-pseudoexon (50× less) and pseudoexon (3× less) containing transcripts in the affected muscle, compared with the level of the non-pseudoexon containing transcript in a control muscle, resulting in very low dystrophin protein levels and the upregulation of utrophin. Because the variant was only found in the affected dog, not in the healthy mother and grandmother, or in 108 unrelated Border Collies from the Belgian population (46 males and 62 females), it was considered a de novo variant. Although the prognosis for dystrophinopathy is generally regarded as poor, the dog stabilised at the age of 6 months and is still clinically stable at the age of 2 years.
Keyphrases
- muscular dystrophy
- duchenne muscular dystrophy
- rna seq
- skeletal muscle
- single cell
- copy number
- molecular dynamics
- genome wide
- ultrasound guided
- small molecule
- cell proliferation
- photodynamic therapy
- gene expression
- signaling pathway
- dna methylation
- transcription factor
- machine learning
- protein kinase
- electronic health record
- subarachnoid hemorrhage
- big data
- brain injury
- binding protein
- tyrosine kinase
- genome wide identification
- body composition
- resistance training