Dolnick B J, Berenson R J, Bertino J R, Kaufman R J, Nunberg J H, Schimke R T
J Cell Biol. 1979 Nov;83(2 Pt 1):394-402. doi: 10.1083/jcb.83.2.394.
A methotrexate (MTX)-resistant murine lymphoblastoid cell line has been obtained by serial passage in increasing concentrations of MTX which is greater than 100,000-fold resistant to MTX (L5178YR) and has dihydrofolate reductase (DHFR) levels 300-fold higher than the parental line. The L5178YR cell line synthesizes approximately 10-11% of its total soluble cell protein as DHFR regardless of growth phase, as measured by direct immunoprecipitation with a monospecific antiserum. Molecular hybridization of a purified [3H]DNA probe complimentary to DHFR specific mRNA with cellular DNA and RNA indicates that DHFR coding sequences are elevated several hundred fold in both nucleic acid species in the mutant cell line. Giemsa-banding studies of the diploid mutant line indicate the presence of a large homogeneously staining region on chromosome No. 2. In situ molecular hybridization studies indicate that the DHFR genes are localized in this homogeneously staining region. The homogeneously staining region probably consists of tandom repeats of a basic segment approximately 800 kilo base pairs long.
通过在浓度不断增加的甲氨蝶呤(MTX)中连续传代,已获得一株对MTX耐药的小鼠淋巴母细胞系,其对MTX的耐药性大于100,000倍(L5178YR),二氢叶酸还原酶(DHFR)水平比亲代细胞系高300倍。用单特异性抗血清进行直接免疫沉淀测定,无论处于生长阶段如何,L5178YR细胞系合成的总可溶性细胞蛋白中约10 - 11%为DHFR。用与DHFR特异性mRNA互补的纯化[3H]DNA探针与细胞DNA和RNA进行分子杂交表明,突变细胞系的两种核酸中DHFR编码序列均升高了数百倍。对二倍体突变系进行吉姆萨显带研究表明,在2号染色体上存在一个大的均匀染色区。原位分子杂交研究表明,DHFR基因定位于这个均匀染色区。该均匀染色区可能由大约800千碱基对长的基本片段的串联重复组成。