Chromosome-mediated transfer and amplification of an altered mouse dihydrofolate reductase gene.

D A Haber, R T Schimke
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引用次数: 9

Abstract

We have conferred methotrexate resistance on mouse 3T6 fibroblasts by chromosome-mediated transfer of an altered dihydrofolate reductase gene encoding a highly methotrexate-insensitive enzyme. The methotrexate-resistant 3T6 cell line from which the chromosomes were prepared contains multiple copies of the altered dihydrofolate reductase gene, all of which appear to reside on double-minute chromosomes. Transformants selected at 0.2 microM methotrexate contain 10-20 times more of the transferred altered gene than of the resident normal gene. The altered genes are associated with double-minute chromosomes and are permanently lost following growth of the transformants in the absence of methotrexate. Growth of the transformants in increasing concentrations of methotrexate leads to the emergence of cells which have accumulated double-minute chromosomes and which have amplified only the transferred dihydrofolate reductase gene.

染色体介导的小鼠二氢叶酸还原酶基因的转移和扩增。
我们通过染色体介导的改变的二氢叶酸还原酶基因的转移,赋予小鼠3T6成纤维细胞甲氨蝶呤抗性,该基因编码一种高度甲氨蝶呤不敏感的酶。制备染色体的抗甲氨蝶呤3T6细胞系含有改变的二氢叶酸还原酶基因的多个拷贝,所有这些基因似乎都位于双分钟染色体上。在0.2微米甲氨蝶呤条件下选择的转化子含有10-20倍的转移的改变基因,而不是常驻的正常基因。改变的基因与双分钟染色体有关,在缺乏甲氨蝶呤的情况下,随着转化子的生长,这些基因将永久丢失。在增加的甲氨蝶呤浓度下,转化子的生长导致细胞出现,这些细胞积累了双分钟染色体,并且只扩增了转移的二氢叶酸还原酶基因。
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