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Congenital myasthenic syndrome in Golden Retrievers is associated with a novel COLQ mutation

BACKGROUND: Congenital myasthenic syndromes (CMSs) are a group of inherited disorders of neuromuscular transmission that may be presynaptic, synaptic, or postsynaptic. Causative mutations have been identified in 4 breeds including the Labrador Retriever, Jack Russell Terrier, Heideterrier, and Danis...

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Autores principales: Tsai, Kate L., Vernau, Karen M., Winger, Kathryn, Zwueste, Danielle M., Sturges, Beverly K., Knipe, Marguerite, Williams, D. Colette, Anderson, Kendall J., Evans, Jacquelyn M., Guo, Ling T., Clark, Leigh Anne, Shelton, G. Diane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6979411/
https://www.ncbi.nlm.nih.gov/pubmed/31769119
http://dx.doi.org/10.1111/jvim.15667
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author Tsai, Kate L.
Vernau, Karen M.
Winger, Kathryn
Zwueste, Danielle M.
Sturges, Beverly K.
Knipe, Marguerite
Williams, D. Colette
Anderson, Kendall J.
Evans, Jacquelyn M.
Guo, Ling T.
Clark, Leigh Anne
Shelton, G. Diane
author_facet Tsai, Kate L.
Vernau, Karen M.
Winger, Kathryn
Zwueste, Danielle M.
Sturges, Beverly K.
Knipe, Marguerite
Williams, D. Colette
Anderson, Kendall J.
Evans, Jacquelyn M.
Guo, Ling T.
Clark, Leigh Anne
Shelton, G. Diane
author_sort Tsai, Kate L.
collection PubMed
description BACKGROUND: Congenital myasthenic syndromes (CMSs) are a group of inherited disorders of neuromuscular transmission that may be presynaptic, synaptic, or postsynaptic. Causative mutations have been identified in 4 breeds including the Labrador Retriever, Jack Russell Terrier, Heideterrier, and Danish Pointing Dog. HYPOTHESIS/OBJECTIVE: Clinical and genetic characterization of a neuromuscular disorder in Golden Retriever (GR) puppies. ANIMALS: Four GR puppies from California were evaluated for generalized muscle weakness beginning at weaning. Biological specimens were collected from the affected puppies, and familial information was obtained. Blood or buccal swabs were obtained from 63 unaffected GRs. METHODS: Complete physical, neurological, electrodiagnostic, and histological evaluations and biochemical quantification of muscle acetylcholine receptors were performed. Polymerase chain reaction was used to amplify the 17 exons of COLQ, and sequences were obtained by Sanger sequencing. Variant frequency was assessed in unrelated GRs and a public database. RESULTS: Clinical, neurological, and electrodiagnostic evaluations confirmed a disorder of neuromuscular transmission in a GR family. Sequencing of all exons and splice sites of a primary candidate gene, COLQ, identified a point mutation that predicts an amino acid substitution (G294R). The primary COLQ transcript was absent from affected muscle samples. All affected puppies were homozygous for the mutation, which was not detected outside this GR family or in other breeds. CONCLUSIONS AND CLINICAL IMPORTANCE: We confirmed the diagnosis of a CMS in GR puppies and identified a novel COLQ mutation. The COLQ gene encodes the collagenous tail of acetylcholinesterase, the enzyme responsible for termination of skeletal muscle contraction by clearing acetylcholine at the neuromuscular junction. Clinicians and breeders should be aware of this CMS in GR puppies with an early onset of weakness.
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spelling pubmed-69794112020-01-29 Congenital myasthenic syndrome in Golden Retrievers is associated with a novel COLQ mutation Tsai, Kate L. Vernau, Karen M. Winger, Kathryn Zwueste, Danielle M. Sturges, Beverly K. Knipe, Marguerite Williams, D. Colette Anderson, Kendall J. Evans, Jacquelyn M. Guo, Ling T. Clark, Leigh Anne Shelton, G. Diane J Vet Intern Med SMALL ANIMAL BACKGROUND: Congenital myasthenic syndromes (CMSs) are a group of inherited disorders of neuromuscular transmission that may be presynaptic, synaptic, or postsynaptic. Causative mutations have been identified in 4 breeds including the Labrador Retriever, Jack Russell Terrier, Heideterrier, and Danish Pointing Dog. HYPOTHESIS/OBJECTIVE: Clinical and genetic characterization of a neuromuscular disorder in Golden Retriever (GR) puppies. ANIMALS: Four GR puppies from California were evaluated for generalized muscle weakness beginning at weaning. Biological specimens were collected from the affected puppies, and familial information was obtained. Blood or buccal swabs were obtained from 63 unaffected GRs. METHODS: Complete physical, neurological, electrodiagnostic, and histological evaluations and biochemical quantification of muscle acetylcholine receptors were performed. Polymerase chain reaction was used to amplify the 17 exons of COLQ, and sequences were obtained by Sanger sequencing. Variant frequency was assessed in unrelated GRs and a public database. RESULTS: Clinical, neurological, and electrodiagnostic evaluations confirmed a disorder of neuromuscular transmission in a GR family. Sequencing of all exons and splice sites of a primary candidate gene, COLQ, identified a point mutation that predicts an amino acid substitution (G294R). The primary COLQ transcript was absent from affected muscle samples. All affected puppies were homozygous for the mutation, which was not detected outside this GR family or in other breeds. CONCLUSIONS AND CLINICAL IMPORTANCE: We confirmed the diagnosis of a CMS in GR puppies and identified a novel COLQ mutation. The COLQ gene encodes the collagenous tail of acetylcholinesterase, the enzyme responsible for termination of skeletal muscle contraction by clearing acetylcholine at the neuromuscular junction. Clinicians and breeders should be aware of this CMS in GR puppies with an early onset of weakness. John Wiley & Sons, Inc. 2019-11-26 2020 /pmc/articles/PMC6979411/ /pubmed/31769119 http://dx.doi.org/10.1111/jvim.15667 Text en © 2019 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals, Inc. on behalf of the American College of Veterinary Internal Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle SMALL ANIMAL
Tsai, Kate L.
Vernau, Karen M.
Winger, Kathryn
Zwueste, Danielle M.
Sturges, Beverly K.
Knipe, Marguerite
Williams, D. Colette
Anderson, Kendall J.
Evans, Jacquelyn M.
Guo, Ling T.
Clark, Leigh Anne
Shelton, G. Diane
Congenital myasthenic syndrome in Golden Retrievers is associated with a novel COLQ mutation
title Congenital myasthenic syndrome in Golden Retrievers is associated with a novel COLQ mutation
title_full Congenital myasthenic syndrome in Golden Retrievers is associated with a novel COLQ mutation
title_fullStr Congenital myasthenic syndrome in Golden Retrievers is associated with a novel COLQ mutation
title_full_unstemmed Congenital myasthenic syndrome in Golden Retrievers is associated with a novel COLQ mutation
title_short Congenital myasthenic syndrome in Golden Retrievers is associated with a novel COLQ mutation
title_sort congenital myasthenic syndrome in golden retrievers is associated with a novel colq mutation
topic SMALL ANIMAL
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6979411/
https://www.ncbi.nlm.nih.gov/pubmed/31769119
http://dx.doi.org/10.1111/jvim.15667
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