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A canine BCAN microdeletion associated with episodic falling syndrome
Episodic falling syndrome (EFS) is a canine paroxysmal hypertonicity disorder found in Cavalier King Charles spaniels. Episodes are triggered by exercise, stress or excitement and characterized by progressive hypertonicity throughout the thoracic and pelvic limbs, resulting in a characteristic '...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Academic Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3898273/ https://www.ncbi.nlm.nih.gov/pubmed/21821125 http://dx.doi.org/10.1016/j.nbd.2011.07.014 |
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author | Gill, Jennifer L. Tsai, Kate L. Krey, Christa Noorai, Rooksana E. Vanbellinghen, Jean-François Garosi, Laurent S. Shelton, G. Diane Clark, Leigh Anne Harvey, Robert J. |
author_facet | Gill, Jennifer L. Tsai, Kate L. Krey, Christa Noorai, Rooksana E. Vanbellinghen, Jean-François Garosi, Laurent S. Shelton, G. Diane Clark, Leigh Anne Harvey, Robert J. |
author_sort | Gill, Jennifer L. |
collection | PubMed |
description | Episodic falling syndrome (EFS) is a canine paroxysmal hypertonicity disorder found in Cavalier King Charles spaniels. Episodes are triggered by exercise, stress or excitement and characterized by progressive hypertonicity throughout the thoracic and pelvic limbs, resulting in a characteristic 'deer-stalking' position and/or collapse. We used a genome-wide association strategy to map the EFS locus to a 3.48 Mb critical interval on canine chromosome 7. By prioritizing candidate genes on the basis of biological plausibility, we found that a 15.7 kb deletion in BCAN, encoding the brain-specific extracellular matrix proteoglycan brevican, is associated with EFS. This represents a compelling causal mutation for EFS, since brevican has an essential role in the formation of perineuronal nets governing synapse stability and nerve conduction velocity. Mapping of the deletion breakpoint enabled the development of Multiplex PCR and Multiplex Ligation-dependent Probe Amplification (MLPA) genotyping tests that can accurately distinguish normal, carrier and affected animals. Wider testing of a larger population of CKCS dogs without a history of EFS from the USA revealed that carriers are extremely common (12.9%). The development of molecular genetic tests for the EFS microdeletion will allow the implementation of directed breeding programs aimed at minimizing the number of animals with EFS and enable confirmatory diagnosis and pharmacotherapy of affected dogs. |
format | Online Article Text |
id | pubmed-3898273 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Academic Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-38982732014-01-24 A canine BCAN microdeletion associated with episodic falling syndrome Gill, Jennifer L. Tsai, Kate L. Krey, Christa Noorai, Rooksana E. Vanbellinghen, Jean-François Garosi, Laurent S. Shelton, G. Diane Clark, Leigh Anne Harvey, Robert J. Neurobiol Dis Article Episodic falling syndrome (EFS) is a canine paroxysmal hypertonicity disorder found in Cavalier King Charles spaniels. Episodes are triggered by exercise, stress or excitement and characterized by progressive hypertonicity throughout the thoracic and pelvic limbs, resulting in a characteristic 'deer-stalking' position and/or collapse. We used a genome-wide association strategy to map the EFS locus to a 3.48 Mb critical interval on canine chromosome 7. By prioritizing candidate genes on the basis of biological plausibility, we found that a 15.7 kb deletion in BCAN, encoding the brain-specific extracellular matrix proteoglycan brevican, is associated with EFS. This represents a compelling causal mutation for EFS, since brevican has an essential role in the formation of perineuronal nets governing synapse stability and nerve conduction velocity. Mapping of the deletion breakpoint enabled the development of Multiplex PCR and Multiplex Ligation-dependent Probe Amplification (MLPA) genotyping tests that can accurately distinguish normal, carrier and affected animals. Wider testing of a larger population of CKCS dogs without a history of EFS from the USA revealed that carriers are extremely common (12.9%). The development of molecular genetic tests for the EFS microdeletion will allow the implementation of directed breeding programs aimed at minimizing the number of animals with EFS and enable confirmatory diagnosis and pharmacotherapy of affected dogs. Academic Press 2012-01 /pmc/articles/PMC3898273/ /pubmed/21821125 http://dx.doi.org/10.1016/j.nbd.2011.07.014 Text en © 2012 Elsevier Inc. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license |
spellingShingle | Article Gill, Jennifer L. Tsai, Kate L. Krey, Christa Noorai, Rooksana E. Vanbellinghen, Jean-François Garosi, Laurent S. Shelton, G. Diane Clark, Leigh Anne Harvey, Robert J. A canine BCAN microdeletion associated with episodic falling syndrome |
title | A canine BCAN microdeletion associated with episodic falling syndrome |
title_full | A canine BCAN microdeletion associated with episodic falling syndrome |
title_fullStr | A canine BCAN microdeletion associated with episodic falling syndrome |
title_full_unstemmed | A canine BCAN microdeletion associated with episodic falling syndrome |
title_short | A canine BCAN microdeletion associated with episodic falling syndrome |
title_sort | canine bcan microdeletion associated with episodic falling syndrome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3898273/ https://www.ncbi.nlm.nih.gov/pubmed/21821125 http://dx.doi.org/10.1016/j.nbd.2011.07.014 |
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