Kurdi-Haidar B, Levine F, Roemer K, LaPorte P, Friedmann T
Center for Molecular Genetics, UCSD School of Medicine, La Jolla 92093-0634.
Genomics. 1993 Feb;15(2):305-10. doi: 10.1006/geno.1993.1061.
To design a strategy for more efficient long-range physical mapping of large mammalian genomes, we have developed a method for directional mapping from anchor points of randomly integrated retroviral proviruses containing sequences that provide unique cleavage sites in the genome. Using this method, we have determined a physical map of approximately 1.6 Mb flanking an Mo MLV-proviral integration site in mouse NIH/3T3 cells. Our results indicate that this provirus-anchored long-range (PAL) mapping strategy, which uses only two proviral sequences as universal hybridization probes, can potentially allow rapid construction of physical maps for chromosomal regions devoid of other genetic markers.
为设计一种更高效的大型哺乳动物基因组远距离物理图谱绘制策略,我们开发了一种从随机整合的逆转录病毒前病毒的锚定位点进行定向图谱绘制的方法,这些前病毒含有在基因组中提供独特切割位点的序列。使用这种方法,我们确定了小鼠NIH/3T3细胞中一个莫洛尼鼠白血病病毒(Mo MLV)前病毒整合位点两侧约1.6 Mb的物理图谱。我们的结果表明,这种仅使用两个前病毒序列作为通用杂交探针的前病毒锚定远距离(PAL)图谱绘制策略,有可能快速构建缺乏其他遗传标记的染色体区域的物理图谱。