Fuscoe J C, Ockey C H, Fox M
Int J Radiat Biol Relat Stud Phys Chem Med. 1986 Jun;49(6):1011-20. doi: 10.1080/09553008514553231.
Spontaneous and X-ray-induced mutants at the hypoxanthine phosphoribosyl transferase (HPRT) locus have been isolated from V79 Chinese hamster cells and characterized at the biochemical and cytogenetic levels. Fourteen spontaneous and 24 X-ray-induced clones were azaguanine and thioguanine resistant, did not grow in HAT medium (AZRTGRHATS) and failed to incorporate significant levels of [14C]hypoxyanthine. Cytogenetic analysis of two spontaneous and eight X-ray-induced mutants revealed no major X chromosome rearrangements. In two induced mutants, one of which was hypotetraploid (mode 35-39) with 2 X chromosomes, the short arm of the chromosome (Xp) was slightly shorter than normal. A third mutant was hyperdiploid (mode 22-23) compared with the parental clone (mode 21). When compared with wild-type clones, no other cytogenetic changes were evident in the remaining mutants. Analysis at the DNA level using a Chinese hamster HPRT cDNA probe showed major deletion of HPRT sequences in two and partial deletion in another two induced mutants. In two of the mutants with deletions of HPRT sequences there was a visible shortening of the Xp arm. In the other six mutants two spontaneous and four induced) no karyotypic changes or alterations in restriction fragment patterns were detected suggesting that they carry small deletions or point mutations at the HPRT locus.
从V79中国仓鼠细胞中分离出次黄嘌呤磷酸核糖基转移酶(HPRT)位点的自发突变体和X射线诱导突变体,并在生化和细胞遗传学水平上进行了表征。14个自发克隆和24个X射线诱导克隆对氮杂鸟嘌呤和硫代鸟嘌呤具有抗性,在HAT培养基中不生长(AZRTGRHATS),且未能掺入显著水平的[14C]次黄嘌呤。对两个自发突变体和八个X射线诱导突变体的细胞遗传学分析显示,没有主要的X染色体重排。在两个诱导突变体中,其中一个是具有两条X染色体的亚四倍体(众数35 - 39),染色体短臂(Xp)略短于正常。与亲本克隆(众数21)相比,第三个突变体是超二倍体(众数22 - 23)。与野生型克隆相比,其余突变体没有明显的其他细胞遗传学变化。使用中国仓鼠HPRT cDNA探针在DNA水平进行分析表明,在两个诱导突变体中HPRT序列发生了主要缺失,在另外两个诱导突变体中发生了部分缺失。在两个HPRT序列缺失的突变体中,Xp臂明显缩短。在其他六个突变体(两个自发突变体和四个诱导突变体)中,未检测到核型变化或限制性片段模式改变,这表明它们在HPRT位点携带小缺失或点突变。