Giulotto E, Knights C, Stark G R
Cell. 1987 Mar 13;48(5):837-45. doi: 10.1016/0092-8674(87)90080-8.
Baby hamster kidney (BHK) cells selected simultaneously with N-phosphonacetyl-L-aspartate (PALA) and methotrexate (MTX) gave rise to doubly resistant colonies at frequencies 20 to 260 times greater than the product of the independent frequencies found with PALA or MTX alone. Double resistance was due to amplification of both target genes, CAD and DHFR. Four independent doubly resistant "MP" lines were selected and characterized. Cells resistant to coformycin, pyrazofurin, or ouabain were generated from all four MP lines at rates up to 25 times greater than the rates for BHK cells. These three drugs select cells that have amplified the genes for their target enzymes. Therefore, we conclude that the four MP lines have an amplificator phenotype. All four grew much more slowly than BHK cells, indicating that the amplificator phenotype may be linked to significant defects in metabolism or cell division.
用N-膦酰乙酰-L-天冬氨酸(PALA)和甲氨蝶呤(MTX)同时筛选的幼仓鼠肾(BHK)细胞,产生双抗菌落的频率比单独使用PALA或MTX时独立频率的乘积高20至260倍。双重抗性是由于两个靶基因CAD和二氢叶酸还原酶(DHFR)的扩增。选择并鉴定了四个独立的双抗“MP”细胞系。从所有四个MP细胞系中产生对助间型霉素、吡唑呋林或哇巴因耐药的细胞,其产生率比BHK细胞的产生率高25倍。这三种药物筛选出已扩增其靶酶基因的细胞。因此,我们得出结论,这四个MP细胞系具有扩增子表型。所有四个细胞系的生长都比BHK细胞慢得多,这表明扩增子表型可能与代谢或细胞分裂中的重大缺陷有关。