Groffen J, Heisterkamp N, Spurr N, Dana S, Wasmuth J J, Stephenson J R
Nucleic Acids Res. 1983 Sep 24;11(18):6331-9. doi: 10.1093/nar/11.18.6331.
A molecular probe was prepared with specificity for the human cellular homologue of transforming sequences represented within the McDonough strain of feline sarcoma virus (v-fms). By analysis of a series of mouse-human somatic cell hybrids containing variable complements of human chromosomes it was possible to assign this human oncogene, designated c-fms, to chromosome 5. Regional localization of c-fms to band q34 on chromosome 5 was accomplished by analysis of Chinese hamster-human cell hybrids containing as their only human components, terminal and interstitial deleted forms of chromosome 5. The localization of c-fms to chromosome 5 (q34) is of interest in view of reports of a specific, apparently interstitial, deletion involving approximately two thirds of the q arm of chromosome 5 in acute myelogenous leukemia cells.
制备了一种分子探针,它对猫肉瘤病毒(v-fms)麦克多诺株中所含转化序列的人类细胞同源物具有特异性。通过分析一系列含有不同人类染色体互补体的小鼠-人类体细胞杂种,有可能将这个命名为c-fms的人类癌基因定位于5号染色体。通过分析以5号染色体的末端和中间缺失形式作为其唯一人类成分的中国仓鼠-人类细胞杂种,完成了c-fms在5号染色体q34带的区域定位。鉴于有报道称急性髓性白血病细胞中存在涉及5号染色体q臂约三分之二的特异性、明显的中间缺失,c-fms定位于5号染色体(q34)这一结果很有意思。