Bulldog dwarfism in Dexter cattle is caused by mutations in ACAN

被引:59
|
作者
Cavanagh, Julie A. L.
Tammen, Imke
Windsor, Peter A.
Bateman, John F.
Savarirayan, Ravi
Nicholas, Frank W.
Raadsma, Herman W.
机构
[1] Univ Sydney, Raadsma ReproGen, Camden, NSW 2570, Australia
[2] Univ Sydney, Sydney, NSW 2570, Australia
[3] Royal Childrens Hosp, Murdoch Children Res Inst, Musculoskeletal Disorders Theme, Parkville, Vic 3052, Australia
[4] Univ Melbourne, Dept Pediat, Melbourne, Vic 3052, Australia
关键词
D O I
10.1007/s00335-007-9066-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bulldog dwarfism in Dexter cattle is one of the earliest single-locus disorders described in animals. Affected fetuses display extreme disproportionate dwarfism, reflecting abnormal cartilage development (chondrodysplasia). Typically, they die around the seventh month of gestation, precipitating a natural abortion. Heterozygotes show a milder form of dwarfism, most noticeably having shorter legs. Homozygosity mapping in candidate regions in a small Dexter pedigree suggested aggrecan (ACAN) as the most likely candidate gene. Mutation screening revealed a 4-bp insertion in exon 11 (2266_2267insGGCA) (called BD1 for diagnostic testing) and a second, rarer transition in exon 1 (-198C > T) (called BD2) that cosegregate with the disorder. In chondrocytes from cattle heterozygous for the insertion, mutant mRNA is subject to nonsense-mediated decay, showing only 8% of normal expression. Genotyping in Dexter families throughout the world shows a one-to-one correspondence between genotype and phenotype at this locus. The heterozygous and homozygous-affected Dexter cattle could prove invaluable as a model for human disorders caused by mutations in ACAN.
引用
收藏
页码:808 / 814
页数:7
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