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  3. A Missense Variant in ALDH5A1 Associated with Canine Succinic Semialdehyde Dehydrogenase Deficiency (SSADHD) in the Saluki Dog.

A Missense Variant in ALDH5A1 Associated with Canine Succinic Semialdehyde Dehydrogenase Deficiency (SSADHD) in the Saluki Dog.

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DOI
10.7892/boris.146419
Publisher DOI
10.3390/genes11091033
PubMed ID
32887425
Abstract
Dogs provide highly valuable models of human disease due to the similarity in phenotype presentation and the ease of genetic analysis. Seven Saluki puppies were investigated for neurological abnormalities including seizures and altered behavior. Magnetic resonance imaging showed a diffuse, marked reduction in cerebral cortical thickness, and symmetrical T2 hyperintensity in specific brain regions. Cerebral cortical atrophy with vacuolation (status spongiosus) was noted on necropsy. Genome-wide association study of 7 affected and 28 normal Salukis revealed a genome-wide significantly associated region on CFA 35. Whole-genome sequencing of three confirmed cases from three different litters revealed a homozygous missense variant within the aldehyde dehydrogenase 5 family member A1 (ALDH5A1) gene (XM_014110599.2: c.866G>A; XP_013966074.2: p.(Gly288Asp). ALDH5A1 encodes a succinic semialdehyde dehydrogenase (SSADH) enzyme critical in the gamma-aminobutyric acid neurotransmitter (GABA) metabolic pathway. Metabolic screening of affected dogs showed markedly elevated gamma-hydroxybutyric acid in serum, cerebrospinal fluid (CSF) and brain, and elevated succinate semialdehyde in urine, CSF and brain. SSADH activity in the brain of affected dogs was low. Affected Saluki dogs had striking similarities to SSADH deficiency in humans although hydroxybutyric aciduria was absent in affected dogs. ALDH5A1-related SSADH deficiency in Salukis provides a unique translational large animal model for the development of novel therapeutic strategies.
Date Issued
2020-09-02
Publication Type
Article
Subject(s)
500 Science > 590 Animals (Zoology)
600 Technology > 630 Agriculture
500 Science > 570 Life sciences; biology
600 Technology > 610 Medicine & health
Subjects
4-hydroxybutyric acid ALDH5A1 GABA GWAS SSADHD encephalopathy inborn error of metabolism inherited precision medicine succinic semialdehyde whole-genome sequencing
Language(s)
en
Author(s)
Vernau, Karen M
Struys, Eduard
Letko, Anna  orcid-logo
Institut für Genetik  
Woolard, Kevin D
Aguilar, Miriam
Brown, Emily A
Cissell, Derek D
Dickinson, Peter J
Shelton, G Diane
Broome, Michael R
Gibson, K Michael
Pearl, Phillip L
König, Florian
Van Winkle, Thomas J
O'Brien, Dennis
Roos, B
Matiasek, Kaspar
Jagannathan, Vidya  
Institut für Genetik  
Drögemüller, Cord  orcid-logo
Institut für Genetik  
Mansour, Tamer A
Brown, C Titus
Bannasch, Danika L
Additional Credits
Institut für Genetik  
Journal
Genes
Publisher
MDPI
ISSN
2073-4425
Access(Rights)
open.access
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