Exonic Short Interspersed Nuclear Element Insertion in
FAM161A
SINE
dogs
genetics
homozygosity mapping
inherited eye disease
progressive retinal atrophy
retinitis pigmentosa
whole genome sequencing
Journal
Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097
Informations de publication
Date de publication:
20 Jul 2024
20 Jul 2024
Historique:
received:
19
06
2024
revised:
08
07
2024
accepted:
16
07
2024
medline:
27
7
2024
pubmed:
27
7
2024
entrez:
27
7
2024
Statut:
epublish
Résumé
Progressive retinal atrophies (PRAs) are a genetically heterogeneous group of inherited eye diseases that affect over 100 breeds of dog. The initial clinical sign is visual impairment in scotopic conditions, as a consequence of rod photoreceptor cell degeneration. Photopic vision degeneration then follows, due to progression of the disease to the cone photoreceptors, and ultimately results in complete blindness. Two full-sibling English Shepherds were diagnosed with PRA at approximately 5 years old and tested clear of all published PRA genetic variants. This study sought to identify the novel PRA-associated variant segregating in the breed. We utilised a combined approach of whole genome sequencing of the probands and homozygosity mapping of four cases and 22 controls and identified a short interspersed nuclear element within an alternatively spliced exon in
Identifiants
pubmed: 39062732
pii: genes15070952
doi: 10.3390/genes15070952
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Dogs Trust
ID : G109751
Organisme : Kennel Club Charitable Trust
ID : G109537