Lange E, Borresen A L, Chen X, Chessa L, Chiplunkar S, Concannon P, Dandekar S, Gerken S, Lange K, Liang T
Department of Pathology, University of California, Los Angeles School of Medicine 90095-1732, USA.
Am J Hum Genet. 1995 Jul;57(1):112-9.
We describe a 20-point linkage analysis map of chromosome 11q22-23 that is based on genotyping 249 families (59 CEPH and 190 A-T). Monte Carlo linkage analyses of 176 ataxia-telangiectasia (A-T) families localizes the major A-T locus to the region between S1819(A4) and S1818(A2). When seven nonlinking families were excluded from subsequent analyses, a 2-lod support interval of approximately 500 kb was identified between S1819(A4) and S1294. No recombinants were observed between A-T and markers S384, B7, S535, or S1294. Only 17 of the international consortium families have been assigned to complementation groups. The available evidence favors either a cluster of A-T genes on chromosome 11 or intragenic defects in a single gene.
我们描述了基于对249个家系(59个CEPH家系和190个共济失调毛细血管扩张症(A-T)家系)进行基因分型的11号染色体q22-23区域的20点连锁分析图谱。对176个共济失调毛细血管扩张症(A-T)家系进行的蒙特卡洛连锁分析将主要的A-T基因座定位到S1819(A4)和S1818(A2)之间的区域。当在后续分析中排除7个非连锁家系后,在S1819(A4)和S1294之间确定了一个约500 kb的2-LOD支持区间。在A-T与标记S384、B7、S535或S1294之间未观察到重组。国际联盟的家系中只有17个已被归入互补组。现有证据支持11号染色体上存在A-T基因簇或单个基因内的缺陷。