Wolf Matthias T F, Karle Stephanie M, Schwarz Stella, Anlauf Mathias, Anlauf Manfred, Glaeser Lisa, Kroiss Sabine, Burton Chris, Feest Terry, Otto Edgar, Fuchshuber Arno, Hildebrandt Friedhelm
Department of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, Michigan 48109-0640, USA.
Kidney Int. 2003 Sep;64(3):788-92. doi: 10.1046/j.1523-1755.2003.00161.x.
Autosomal-dominant medullary cystic kidney disease type 1 (MCKD1) [OMIM 174000] is a hereditary nephropathy that leads to renal salt wasting and end-stage renal failure at a median age of 62 years. In a Welsh MCKD1 kindred we have recently demonstrated linkage to the MCKD1 locus on chromosome 1q23.1 and refined the critical MCKD1 region to <3.3 Mb.
In order to refine the candidate gene region for MCKD1, high-resolution haplotype analysis in three large kindreds with MCKD1 was performed.
We report here on high-resolution haplotype analysis in this Welsh kindred, as well as in the Arizona kindred, which was used for the first definition of MCKD as a disease entity, and in a kindred from the Dutch/German border. We detected extensive haplotype sharing among all affected individuals of all three kindreds. Scrutinization of the genealogy of the Arizona kindred revealed an origin from Germany in the 17th century, thereby providing historical data for haplotype sharing by descent at the MCKD1 locus.
Under the hypothesis of haplotype sharing by descent, we refined the critical genetic interval to <650 kb, thus enabling candidate gene analysis.
常染色体显性遗传性1型髓质囊性肾病(MCKD1)[在线人类孟德尔遗传数据库编号174000]是一种遗传性肾病,可导致肾性失盐,并在62岁左右发展为终末期肾衰竭。在一个威尔士MCKD1家系中,我们最近证实了与1号染色体1q23.1上的MCKD1基因座存在连锁关系,并将关键的MCKD1区域缩小至<3.3 Mb。
为了进一步明确MCKD1的候选基因区域,我们对三个患有MCKD1的大家系进行了高分辨率单倍型分析。
我们在此报告了对这个威尔士家系、亚利桑那家系(该家系首次将MCKD定义为一种疾病实体)以及一个来自荷兰/德国边境的家系进行的高分辨率单倍型分析。我们在所有三个家系的所有患病个体中均检测到广泛的单倍型共享。对亚利桑那家系谱系的详细研究表明其起源于17世纪的德国,从而为通过MCKD1基因座的血缘共享单倍型提供了历史数据。
在血缘共享单倍型的假设下,我们将关键遗传区间缩小至<650 kb,从而能够进行候选基因分析。