Bradley D G, Farrar G J, Sharp E M, Kenna P, Humphries M M, McConnell D J, Daiger S P, McWilliam P, Humphries P
Department of Genetics, Trinity College, Dublin, Republic of Ireland.
Am J Hum Genet. 1989 Apr;44(4):570-6.
Members of a large Irish pedigree exhibiting early-onset autosomal dominant retinitis pigmentosa (ADRP) were typed for the rhesus blood group and nine DNA markers on chromosome 1. Close linkage between the ADRP locus and any of the marker loci was excluded using two-point analysis. With use of the sex-averaged maps of Dracopoli et al. and Donis-Keller et al. and a strategy of rolling multipoint analyses, support was gained for the exclusion of ADRP from a 224-cM region of the chromosome, including almost the entire short arm. The disease locus was significantly excluded from within at least 50 cM of the rhesus locus and, as a loose linkage between these two genes has been suggested by other studies, this result may support the possibility of genetic heterogeneity within the autosomal dominant subgroup of retinitis pigmentosa.
对一个表现出早发性常染色体显性遗传性视网膜色素变性(ADRP)的大型爱尔兰家系成员进行了恒河猴血型分型以及1号染色体上9个DNA标记物的检测。通过两点分析排除了ADRP基因座与任何标记基因座之间的紧密连锁关系。利用Dracopoli等人和Donis-Keller等人的性别平均图谱以及滚动多点分析策略,支持将ADRP从该染色体224厘摩区域排除,该区域几乎包括整个短臂。疾病基因座被显著排除在恒河猴基因座至少50厘摩范围内,并且由于其他研究曾提示这两个基因之间存在松散连锁,该结果可能支持视网膜色素变性常染色体显性亚组内存在遗传异质性的可能性。