Weier H U, Gray J W
Department of Laboratory Medicine, University of California, San Francisco 94143-0808.
Anal Cell Pathol. 1992 Mar;4(2):81-6.
A degenerate alpha satellite DNA probe specific for a repeated sequence on human chromosomes 13 and 21 was synthesized using the polymerase chain reaction (PCR). Fluorescence in situ hybridization (FISH) with this probe to normal metaphase spreads revealed strong probe binding to the centromeric regions of human chromosomes 13 and 21 with negligible cross-hybridization with other chromosomes. FISH to normal interphase cell nuclei showed four distinct domains of probe binding. However, hybridization with probe to interphase and metaphase preparations from one apparently normal human male resulted in only three major binding domains. Metaphase chromosome analysis revealed a centromeric deletion on one chromosome 21 that caused greatly reduced probe binding. The result suggest caution in the interpretation of interphase ploidy studies performed with chromosome-specific alphoid DNA probes.
利用聚合酶链反应(PCR)合成了一种针对人类13号和21号染色体上重复序列的简并α卫星DNA探针。用该探针对正常中期染色体铺展进行荧光原位杂交(FISH),结果显示探针与人类13号和21号染色体的着丝粒区域有强烈结合,与其他染色体的交叉杂交可忽略不计。对正常间期细胞核进行FISH显示有四个不同的探针结合区域。然而,用该探针对一名表面正常的人类男性的间期和中期标本进行杂交时,仅产生了三个主要的结合区域。中期染色体分析显示一条21号染色体存在着丝粒缺失,导致探针结合大大减少。结果提示,在用染色体特异性α卫星DNA探针进行间期倍性研究的解释时应谨慎。