Mignot E, Bell R A, Rattazzi C, Lovett M, Grumet F C, Dement W C
Stanford University, School of Medicine, Sleep Disorders Center, Palo Alto, California.
Sleep. 1994 Dec;17(8 Suppl):S68-76. doi: 10.1093/sleep/17.suppl_8.s68.
Canine narcolepsy is an animal model of the human disorder that is transmitted as a single autosomal recessive gene with full penetrance (canarc-1) in Dobermans and Labradors. In previous experiments, we have identified a very tight linkage marker for canarc-1. This marker, a 0.85-kb band cross reacting with a human mu-switch Heavy-Chain Immunoglobulin probe (maximum logarithm of odds [LOD] score Zmax = 10.8 at 0% recombination), has now been cloned and sequenced. The gene, composed of GC rich repeats, is 75% homologous to the human mu-switch gene and is similar in organization to immunoglobulin switch genes. Curiously, however, this mu-switchlike segment appears to be unlinked with other switchlike polymorphisms detected at high stringency with the human mu-switch probe. Because in most animal species all switch genes are located within 300-500 kb and show tight linkage in families, this result suggests two possible hypotheses: 1) Our 0.85 kb is a true immunoglobulin switch segment, but the map of the canine Variable Heavy-Chain loci is organized in unlinked clusters, or 2) our 0.85-kb segment is not an immunoglobulin switch segment and is located elsewhere in the genome in all species. We are now using chromosome walking and Yeast Artificial Chromosome Cloning techniques, together with corresponding studies in humans to identify the pathological gene.
犬发作性睡病是一种人类疾病的动物模型,在杜宾犬和拉布拉多犬中,它由一个具有完全外显率的常染色体隐性基因(canarc-1)传递。在先前的实验中,我们已经确定了一个与canarc-1紧密连锁的标记。这个标记是一条0.85 kb的条带,它与人类μ-转换重链免疫球蛋白探针发生交叉反应(在0%重组率时,最大优势对数[LOD]分数Zmax = 10.8),现在已经被克隆并测序。该基因由富含GC的重复序列组成,与人类μ-转换基因有75%的同源性,并且在组织结构上与免疫球蛋白转换基因相似。然而,奇怪的是,这个类似μ-转换的片段似乎与用人类μ-转换探针在高严谨度下检测到的其他类似转换的多态性没有连锁关系。因为在大多数动物物种中,所有的转换基因都位于300 - 500 kb范围内,并且在家族中显示出紧密的连锁关系,所以这个结果提出了两个可能的假设:1)我们的0.85 kb片段是一个真正的免疫球蛋白转换片段,但犬可变重链基因座的图谱是由不连锁的簇组成的;或者2)我们的0.85 kb片段不是一个免疫球蛋白转换片段,并且在所有物种的基因组中位于其他位置。我们现在正在使用染色体步移和酵母人工染色体克隆技术,以及在人类中的相应研究来鉴定致病基因。