Hunter Linda S, Sidjanin Duska J, Johnson Jennifer L, Zangerl Barbara, Galibert Francis, Andre Catherine, Kirkness Ewen, Talamas Elijah, Acland Gregory M, Aguirre Gustavo D
J. A. Baker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Mol Vis. 2006 May 24;12:588-96.
To facilitate the molecular characterization of naturally occurring cataracts in dogs by providing the radiation hybrid location of 21 cataract-associated genes along with their closely associated polymorphic markers. These can be used for segregation testing of the candidate genes in canine cataract pedigrees.
Twenty-one genes with known mutations causing hereditary cataracts in man and/or mouse were selected and mapped to canine chromosomes using a canine:hamster radiation hybrid RH5000 panel. Each cataract gene ortholog was mapped in relation to over 3,000 markers including microsatellites, ESTs, genes, and BAC clones. The resulting independently determined RH-map locations were compared with the corresponding gene locations from the draft sequence of the canine genome.
Twenty-one cataract orthologs were mapped to canine chromosomes. The genetic locations and nearest polymorphic markers were determined for 20 of these orthologs. In addition, the resulting cataract gene locations, as determined experimentally by this study, were compared with those determined by the canine genome project. All genes mapped within or near chromosomal locations with previously established homology to the corresponding human gene locations based on canine:human chromosomal synteny.
The location of selected cataract gene orthologs in the dog, along with their nearest polymorphic markers, serves as a resource for association and linkage testing in canine pedigrees segregating inherited cataracts. The recent development of canine genomic resources make canine models a practical and valuable resource for the study of human hereditary cataracts. Canine models can serve as large animal models intermediate between mouse and man for both gene discovery and the development of novel cataract therapies.
通过提供21个白内障相关基因及其紧密相关的多态性标记的辐射杂种定位,促进犬类自然发生白内障的分子特征研究。这些可用于犬类白内障家系中候选基因的分离测试。
选择21个在人类和/或小鼠中已知会导致遗传性白内障的基因突变的基因,并使用犬:仓鼠辐射杂种RH5000面板将其定位到犬类染色体上。每个白内障基因直系同源物都相对于超过3000个标记进行定位,包括微卫星、EST、基因和BAC克隆。将独立确定的RH图谱位置与犬类基因组草图序列中的相应基因位置进行比较。
21个白内障直系同源物被定位到犬类染色体上。确定了其中20个直系同源物的遗传位置和最接近的多态性标记。此外,将本研究实验确定的白内障基因位置与犬类基因组计划确定的位置进行了比较。所有基因都定位在与基于犬:人类染色体同线性先前确定的与相应人类基因位置具有同源性的染色体位置内或附近。
犬类中选定的白内障基因直系同源物的位置及其最接近的多态性标记,可作为在分离遗传性白内障的犬类家系中进行关联和连锁测试的资源。犬类基因组资源的最新发展使犬类模型成为研究人类遗传性白内障的实用且有价值的资源。犬类模型可作为介于小鼠和人类之间的大型动物模型,用于基因发现和新型白内障治疗方法的开发。