A canine BCAN microdeletion associated with episodic falling syndrome

被引:44
作者
Gill, Jennifer L. [2 ]
Tsai, Kate L. [1 ]
Krey, Christa
Noorai, Rooksana E. [1 ]
Vanbellinghen, Jean-Francois [3 ]
Garosi, Laurent S. [4 ]
Shelton, G. Diane [5 ]
Clark, Leigh Anne [1 ]
Harvey, Robert J. [2 ]
机构
[1] Clemson Univ, Dept Biochem & Genet, Coll Agr Forestry & Life Sci, Clemson, SC 29634 USA
[2] Univ London, Sch Pharm, Dept Pharmacol, London WC1N 1AX, England
[3] Inst Pathol & Genet ASBL, B-6041 Gosselies, Belgium
[4] Davies Vet Specialists, Higham Gobion, Herts, England
[5] Univ Calif San Diego, Dept Pathol, La Jolla, CA 92093 USA
基金
英国医学研究理事会;
关键词
Brevican; BCAN; Episodic falling syndrome; Cavalier King Charles spaniels; Microdeletion; KING CHARLES SPANIEL; MUSCLE HYPERTONICITY; STARTLE DISEASE; LINK PROTEIN; GENE; MUTATION; HYPEREKPLEXIA; SUBUNIT; BRAL1; MYOPATHY;
D O I
10.1016/j.nbd.2011.07.014
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:130 / 136
页数:7
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