Peral B, Ward C J, San Millán J L, Thomas S, Stallings R L, Moreno F, Harris P C
MRC Molecular Haematology Unit, Institute of Molecular Medicine, Headington, Oxford, United Kingdom.
Am J Hum Genet. 1994 May;54(5):899-908.
Forty-one Spanish families with polycystic kidney disease 1 (PKD1) were studied for evidence of linkage disequilibrium between the disease locus and six closely linked markers. Four of these loci--three highly polymorphic microsatellites (SM6, CW3, and CW2) and an RFLP marker (BLu24)--are described for the first time in this report. Overall the results reveal many different haplotypes on the disease-carrying chromosome, suggesting a variety of independent PKD1 mutations. However, linkage disequilibrium was found between BLu24 and PKD1, and this was corroborated by haplotype analysis including the microsatellite polymorphisms. From this analysis a group of closely related haplotypes, consisting of four markers, was found on 40% of PKD1 chromosomes, although markers flanking this homogeneous region showed greater variability. This study has highlighted an interesting subpopulation of Spanish PKD1 chromosomes, many of which have a common origin, that may be useful for localizing the PKD1 locus more precisely.
对41个患有多囊肾病1型(PKD1)的西班牙家庭进行了研究,以寻找疾病位点与六个紧密连锁标记之间的连锁不平衡证据。本报告首次描述了其中四个位点——三个高度多态性微卫星(SM6、CW3和CW2)和一个RFLP标记(BLu24)。总体结果显示,携带疾病的染色体上有许多不同的单倍型,提示存在多种独立的PKD1突变。然而,发现BLu24与PKD1之间存在连锁不平衡,包括微卫星多态性的单倍型分析证实了这一点。通过该分析,在40%的PKD1染色体上发现了一组由四个标记组成的密切相关单倍型,尽管该同源区域两侧的标记显示出更大的变异性。这项研究突出了西班牙PKD1染色体中一个有趣的亚群,其中许多具有共同起源,这可能有助于更精确地定位PKD1位点。