Tantravahi U, Stewart G D, Van Keuren M, McNeil G, Roy S, Patterson D, Drabkin H, Lalande M, Kurnit D M, Latt S A
Genetics Division, Children's Hospital, Boston, MA 02115.
Hum Genet. 1988 Jul;79(3):196-202. doi: 10.1007/BF00366237.
By merging two efficient technologies, bivariate flow sorting of human metaphase chromosomes and a recombination-based assay for sequence complexity, we isolated 28 cloned DNA segments homologous to loci on human chromosome 21. Subregional mapping of these DNA segments with a somatic cell hybrid panel showed that 26 of the 28 cloned DNA sequences are distributed along the long arm of chromosome 21, while the other 2 hybridize with sequences on the short arm of both chromosome 21 and other chromosomes. This new collection of probes homologous to chromosome 21 should facilitate molecular analyses of trisomy 21 by providing DNA probes for the linkage map of chromosome 21, for studies of nondisjunction, for chromosome walking in clinically relevant subregions of chromosome 21, and for the isolation of genes on chromosome 21 following the screening of cDNA libraries.
通过将两项高效技术——人类中期染色体的双变量流式分选和基于重组的序列复杂性分析——相结合,我们分离出了28个与人类21号染色体上的基因座同源的克隆DNA片段。利用体细胞杂交板对这些DNA片段进行亚区域定位分析表明,28个克隆DNA序列中的26个沿21号染色体长臂分布,另外2个则与21号染色体短臂以及其他染色体上的序列杂交。这组与21号染色体同源的新探针,通过为21号染色体的连锁图谱研究、不分离现象研究、21号染色体临床相关亚区域的染色体步移以及筛选cDNA文库后分离21号染色体上的基因提供DNA探针,应有助于对21三体综合征进行分子分析。