Kaufman R J, Brown P C, Schimke R T
Proc Natl Acad Sci U S A. 1979 Nov;76(11):5669-73. doi: 10.1073/pnas.76.11.5669.
Selection of mammalian cells in progressively increasing concentrations of methotrexate results in selective amplification of DNA sequences coding for dihydrofolate reductase (tetrahydrofolate dehydrogenase, 5,6,7,8-tetrahydrofolate:NADP+ oxidoreductase, EC 1.5.1.3). In some cell variants the amplified genes are stable with growth in the absence of methotrexate, whereas in other variants the amplified genes are lost from the population. We have previously reported that in a stably amplified variant of Chinese hamster ovary cells, the genes are localized to a single chromosome. Herein we report that in mouse S-180 and L5178Y cell lines unstably amplified dihydrofolate reductase DNA sequences are associated with small, paired chromosomal elements denoted "double minute chromosomes," whereas in stably amplified cells of the same origin, the genes are associated with large chromosomes.
在逐步增加浓度的甲氨蝶呤中选择哺乳动物细胞,会导致编码二氢叶酸还原酶(四氢叶酸脱氢酶、5,6,7,8 - 四氢叶酸:NADP⁺氧化还原酶,EC 1.5.1.3)的DNA序列选择性扩增。在一些细胞变体中,扩增的基因在无甲氨蝶呤的情况下生长时是稳定的,而在其他变体中,扩增的基因会从群体中丢失。我们之前报道过,在中国仓鼠卵巢细胞的一个稳定扩增变体中,这些基因定位于一条单一染色体上。在此我们报道,在小鼠S - 180和L5178Y细胞系中,不稳定扩增的二氢叶酸还原酶DNA序列与被称为“双微小染色体”的小的、成对的染色体元件相关,而在相同来源的稳定扩增细胞中,这些基因与大染色体相关。