Tam S Y, Geissler E N, Graw S L, Housman D E
Center for Cancer Research, Massachusetts Institute of Technology, Cambridge 02139.
Mol Cell Biol. 1990 Dec;10(12):6619-23. doi: 10.1128/mcb.10.12.6619-6623.1990.
The entire 33-kb coding region of the mouse Na,K-ATPase alpha 1 subunit gene was cloned in two overlapping cosmids which contain inserts of 40 kb. To assess the functional expression of the mouse alpha 1 gene, the two cosmids were cotransfected into ouabain-sensitive CV-1 monkey cells yielding an average of 64 resistant colonies per 10(6) cells per microgram of DNA. Analysis of the DNA transferred to the ouabain-resistant transformants by the two cosmids suggests that the generation of a functional gene can occur by homologous recombination between the two introduced segments, as demonstrated by generation of a novel diagnostic restriction fragment. The ability to reconstruct the intact mouse alpha 1 gene in a heterologous host cell and to monitor its functional expression with a selection protocol permits direct identification and isolation of regulatory sequences for the gene.
小鼠钠钾ATP酶α1亚基基因的整个33kb编码区被克隆到两个重叠的黏粒中,这些黏粒包含40kb的插入片段。为了评估小鼠α1基因的功能表达,将这两个黏粒共转染到对哇巴因敏感的CV-1猴细胞中,每微克DNA每10⁶个细胞平均产生64个抗性菌落。对通过这两个黏粒转移到对哇巴因抗性的转化体中的DNA进行分析表明,功能性基因的产生可能通过两个导入片段之间的同源重组发生,这一点通过产生一个新的诊断性限制性片段得到了证明。在异源宿主细胞中重建完整小鼠α1基因并通过选择方案监测其功能表达的能力,使得能够直接鉴定和分离该基因的调控序列。