Lebo R V, Lynch E D, Bird T D, Golbus M S, Barker D F, O'Connell P, Chance P F
Department of Obstetrics, University of California, San Francisco 94143-0720.
Am J Hum Genet. 1992 Jan;50(1):42-55.
This study demonstrates a clear and current role for multicolor in situ hybridization in expediting positional cloning studies of unknown disease genes. Nine polymorphic DNA cosmids have been mapped to eight ordered locations spanning the Charcot-Marie-Tooth type 1 (CMT1A) disease gene region in distal band 17p11.2, by multicolor in situ hybridization. When used with linkage analysis, these methods have generated a fine physical map and have firmly assigned the CMT1A gene to distal band 17p11.2. Linkage analysis with four CMT1A pedigrees mapped the CMT1A gene with respect to two flanking markers (8B10-5 cM[LOD 5.2]-CMT1A-3.5 cM[LOD 5.3]-10E4). Additional loci were physically mapped and ordered by in situ hybridization and analysis of phase-known recombinants in CMT1A pedigrees. The order determined by multicolor in situ hybridization was 17cen-LEW301-8B10-5H5/6A9-VAW409- 5G7-6G1-4A11-VAW412-10E4-pter. Two ordered probes, 4A11 and 6G1, reside on the same 440-kb partial SfiI restriction fragment. These data demonstrate the ability of in situ hybridization to resolve loci within 0.5 Mb on early-metaphase chromosomes. Multicolor in situ hybridization also excluded the possibility of pericentric inversions in two unrelated patients with CMT1 and neurofibromatosis type 1. When used with pulsed-field gel electrophoresis, multicolor in situ hybridization can establish physical location, order, and distance in closely spaced chromosome loci.
本研究证明了多色原位杂交在加速未知疾病基因定位克隆研究中目前具有明确作用。通过多色原位杂交,已将9个多态性DNA黏粒定位到17号染色体短臂11.2区带远端的8个有序位置,这些位置跨越了遗传性运动感觉神经病1型(CMT1A)疾病基因区域。当与连锁分析结合使用时,这些方法构建了精细的物理图谱,并将CMT1A基因明确定位于17号染色体短臂11.2区带远端。对4个CMT1A家系进行连锁分析,将CMT1A基因相对于两个侧翼标记进行了定位(8B10 - 5厘摩[优势对数记分5.2] - CMT1A - 3.5厘摩[优势对数记分5.3] - 10E4)。通过原位杂交以及对CMT1A家系中已知相位的重组体进行分析,对其他位点进行了物理定位和排序。通过多色原位杂交确定的顺序为:17号染色体着丝粒 - LEW301 - 8B10 - 5H5/6A9 - VAW409 - 5G7 - 6G1 - 4A11 - VAW412 - 10E4 - 染色体末端。两个有序探针4A11和6G1位于同一个440kb的部分SfiI限制性片段上。这些数据证明了原位杂交能够在早中期染色体上分辨出0.5Mb以内的位点。多色原位杂交还排除了两名患有CMT1和1型神经纤维瘤病的无关患者存在着丝粒周围倒位的可能性。当与脉冲场凝胶电泳结合使用时,多色原位杂交能够确定紧密间隔的染色体位点的物理位置、顺序和距离。