Xiao Y, Natarajan A T
Department of Radiation Genetics and Chemical Mutagenesis, Leiden University, Leiden, The Netherlands.
Cytogenet Cell Genet. 1998;83(3-4):208-13. doi: 10.1159/000015180.
Arm-specific and subtelomeric region-specific painting probes for Chinese hamster chromosomes have been generated by microdissection and use of the degenerate oligonucleotide-primed polymerase chain reaction (DOP-PCR). Fluorescence in situ hybridization (FISH) analyses using these probes demonstrated their specificity. These probes painted every chromosome arm and a total of 15 subtelomeric regions, namely, both ends of chromosomes 1, 2, 3, 4, and 8 and one end of chromosome arms 5q, 6q, 7q, 9p, and Xp. Many cryptic chromosomal rearrangements in the CHO-9 and V79 cell lines that were not detectable with whole chromosome paints could be recognized when these newly developed probes were used.
通过显微切割以及使用简并寡核苷酸引物聚合酶链反应(DOP-PCR),已生成了针对中国仓鼠染色体的特定染色体臂和亚端粒区域的涂染探针。使用这些探针进行的荧光原位杂交(FISH)分析证明了它们的特异性。这些探针标记了每个染色体臂以及总共15个亚端粒区域,即染色体1、2、3、4和8的两端以及染色体臂5q、6q、7q、9p和Xp的一端。当使用这些新开发的探针时,可以识别出在CHO-9和V79细胞系中许多用全染色体涂染无法检测到的隐匿染色体重排。