Hunter K W, Ontiveros S D, Watson M L, Stanton V P, Gutierrez P, Bhat D, Rochelle J, Graw S, Ton C, Schalling M
Center for Cancer Research, Massachusetts Institute of Technology, Cambridge 02139.
Mamm Genome. 1994 Oct;5(10):597-607. doi: 10.1007/BF00411453.
We have developed a new technique for the generation of YAC contigs in the mouse genome that is based on the ability to detect overlapping clones by hybridization of shared IRS-PCR products. As a demonstration of the technique, a 5-cM, > 5 megabase contig was developed on the distal half of mouse Chromosome (Chr) 1, spanning the region from Lamb2 to At3. The contig covers roughly 5% of the genetic distance of the chromosome and is comprised of more than 80 clones; 71 probes were assigned physical order to the chromosome, of which 59 were new markers generated in this study. Eight of the new probes were shown to be polymorphic between C3H/HeJ-gld and M. spretus. Three probes were mapped on a [(C3H/HeJ-gld x M. spretus) x C3H/HeJ-gld] interspecific backcross to integrate the physical map with a high-resolution genetic map of the region.
我们开发了一种在小鼠基因组中生成酵母人工染色体(YAC)重叠群的新技术,该技术基于通过共享IRS-PCR产物杂交检测重叠克隆的能力。作为该技术的一个实例,在小鼠1号染色体(Chr)远端的后半部分构建了一个5厘摩、大于5兆碱基的重叠群,跨越从Lamb2到At3的区域。该重叠群大约覆盖了该染色体遗传距离的5%,由80多个克隆组成;71个探针被确定在染色体上的物理顺序,其中59个是本研究中产生的新标记。新探针中有8个在C3H/HeJ-gld和西班牙小家鼠之间表现出多态性。三个探针被定位在一个[(C3H/HeJ-gld×西班牙小家鼠)×C3H/HeJ-gld]种间回交群体上,以便将物理图谱与该区域的高分辨率遗传图谱整合起来。