School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW 2052, Australia.
Anim Genet. 2011 Dec;42(6):675-8. doi: 10.1111/j.1365-2052.2011.02199.x. Epub 2011 Apr 14.
An autosomal recessive form of cerebellar abiotrophy occurs in Australian Kelpie dogs. Clinical signs range from mild ataxia with intention tremor to severe ataxia with seizures. A whole-genome mapping analysis was performed using Affymetrix Canine SNP array v2 on 11 affected and 19 control dogs, but there was no significant association with disease. A homozygosity analysis identified a three megabase region likely to contain the disease mutation. The region spans 29.8-33 Mb on chromosome 3, for which all affected dogs were homozygous for a common haplotype. Microsatellite markers were developed in the candidate region for linkage analysis that resulted in a logarithm of odds score suggestive of linkage. The candidate region contains 29 genes, none of which are known to cause ataxia.
小脑萎缩症的常染色体隐性形式发生在澳大利亚牧羊犬中。临床症状从轻微的意向性震颤共济失调到严重的癫痫共济失调不等。使用 Affymetrix Canine SNP 阵列 v2 在 11 只受影响的和 19 只对照犬上进行了全基因组图谱分析,但与疾病没有显著关联。纯合子分析确定了一个可能包含疾病突变的三个兆碱基区域。该区域跨越 3 号染色体上的 29.8-33 Mb,所有受影响的犬都为一个常见单倍型的纯合子。在候选区域开发了微卫星标记用于连锁分析,结果得出了连锁的可能性对数评分。候选区域包含 29 个基因,其中没有一个已知会导致共济失调。