Gardiner K, Watkins P, Münke M, Drabkin H, Jones C, Patterson D
Eleanor Roosevelt Institute for Cancer Research, Denver, Colorado 80206.
Somat Cell Mol Genet. 1988 Nov;14(6):623-37. doi: 10.1007/BF01535316.
The long arm of human chromosome 21 has been analyzed with unique sequence DNA probes, using an expanded panel of somatic cell hybrids containing defined regions of the chromosome, and both standard and pulsed field gel electrophoresis. Each member of the hybrid cell panel contains either a normal chromosome 21, or one of 11 different translocations or deletions within the long arm. Together, these now include 11 breakpoints, defining 11 long arm regions. Thirty-two unique sequence probes have been localized to these regions by standard gel electrophoresis. Analysis by pulsed field gels indicates that 27 of these identify a total of 18 Not1 restriction fragments, which together account for approximately 17 million base pairs, over half the long arm. Five physical linkage groups have been identified, as well as patterns in the distribution of unique sequences and GC-rich chromosomal regions. This information can be correlated with that obtained by other methods and contributes to the construction of a detailed physical map of this chromosome.
利用一组扩展的含有该染色体特定区域的体细胞杂种,并结合标准和脉冲场凝胶电泳技术,使用独特序列DNA探针分析了人类21号染色体的长臂。杂种细胞面板中的每个成员要么含有一条正常的21号染色体,要么含有长臂内11种不同易位或缺失中的一种。这些易位和缺失现在总共包括11个断点,界定了11个长臂区域。通过标准凝胶电泳已将32个独特序列探针定位到这些区域。脉冲场凝胶分析表明,其中27个探针识别出总共18个Not1限制性片段,这些片段加起来约为1700万个碱基对,超过长臂的一半。已确定了5个物理连锁群,以及独特序列和富含GC的染色体区域的分布模式。这些信息可与通过其他方法获得的信息相关联,并有助于构建该染色体的详细物理图谱。