Choo K H, Filby G, Earle E, Brown R
Murdoch Institute, Royal Children's Hospital, Melbourne, Victoria, Australia.
Hum Genet. 1988 Dec;81(1):49-53. doi: 10.1007/BF00283728.
We report the isolation of 50 independent unique sequences from a human chromosome 21 library (identification code LA21 NSO1). These sequences were individually assigned to chromosome 21 using a mouse-human somatic hybrid cell line, WAVR 4d-F94a. Use of these unique clones as a mixture of probes for in situ hybridization of human metaphase chromosomes demonstrated strong signals on chromosome 21. These unique DNA sequences should provide useful tools for structural and functional analysis of human chromosome 21. The use of these sequences for the detection of Down syndrome is discussed.
我们报道了从一个人类21号染色体文库(识别码LA21 NSO1)中分离出50个独立的独特序列。使用小鼠-人类体细胞杂交细胞系WAVR 4d-F94a将这些序列分别定位到21号染色体上。将这些独特克隆作为探针混合物用于人类中期染色体的原位杂交,结果显示在21号染色体上有强烈信号。这些独特的DNA序列应为人类21号染色体的结构和功能分析提供有用的工具。本文还讨论了利用这些序列检测唐氏综合征的情况。