Ashman C R, Davidson R L
Mol Cell Biol. 1984 Nov;4(11):2266-72. doi: 10.1128/mcb.4.11.2266-2272.1984.
The recombinant shuttle vector pSV2gpt was introduced into V79 Chinese hamster cells, and stable transformants expressing the Escherichia coli gpt gene were selected. Two transformants carrying tandem duplications of the plasmid at a single site were identified and fused to simian COS-1 cells. Plasmid DNA recovered from the heterokaryons was used to transform a Gpt- derivative of E. coli HB101, and the relative frequency of plasmids carrying a mutation in the gpt gene was determined. The high frequency of Gpt- plasmids (ca. 1%) was similar to that observed when plasmid was recovered from COS-1 cells which had been transfected with pSV2gpt. Most of the mutant plasmids had rearrangements in the region containing the gpt gene.
将重组穿梭载体pSV2gpt导入V79中国仓鼠细胞,筛选出表达大肠杆菌gpt基因的稳定转化体。鉴定出两个在单个位点携带质粒串联重复的转化体,并将其与猴COS-1细胞融合。从异核体中回收的质粒DNA用于转化大肠杆菌HB101的Gpt-衍生物,并测定携带gpt基因突变的质粒的相对频率。Gpt-质粒的高频率(约1%)与从用pSV2gpt转染的COS-1细胞中回收质粒时观察到的频率相似。大多数突变质粒在包含gpt基因的区域发生了重排。