Kopnin B P, Gudkov A V
Genetika. 1983 Jun;19(6):864-71.
DNA-mediated transfer of colchicine-resistance from Djungarian hamster DM5/7 cell line, 750-fold resistant to the drug, was studied. The resistance to colchicine of DM5/7 cells is due to amplification of the genes, possibly coding for the polypeptide p22. Both high-molecular weight DNA (presumably, chromosomal DNA) and low-molecular weight DNA (presumably, extrachromosomal DNA) effectively transferred the colchicine-resistance to Djungarian hamster and mouse cells. DNA of sensitive to colchicine but resistant to ouabain mouse cells CAK-143OuaR was not capable to transfer colchicine-resistance, but effectively transferred ouabain-resistance connected with a mutation in Na+/K+-dependent ATP-ase locus. The differences in genetic transformation with amplified p22 genes and mutant Na+/K+-dependent ATP-ase genes were revealed. All cells of 3 colchicine-resistant transformants of DM-15 cells and all 10 spontaneously derived resistant clones contain the additional chromosome 4. The role of trisomy 4 in the development of colchicine-resistance in DM-15 cells is discussed.
研究了通过DNA介导将来自对秋水仙碱有750倍抗性的黑线仓鼠DM5/7细胞系的秋水仙碱抗性进行转移的情况。DM5/7细胞对秋水仙碱的抗性归因于基因扩增,这些基因可能编码多肽p22。高分子量DNA(大概是染色体DNA)和低分子量DNA(大概是染色体外DNA)都有效地将秋水仙碱抗性转移到了黑线仓鼠和小鼠细胞中。对秋水仙碱敏感但对哇巴因抗性的小鼠细胞CAK-143OuaR的DNA不能转移秋水仙碱抗性,但能有效地转移与Na+/K+依赖性ATP酶基因座突变相关的哇巴因抗性。揭示了用扩增的p22基因和突变的Na+/K+依赖性ATP酶基因进行遗传转化的差异。DM-15细胞的3个抗秋水仙碱转化体的所有细胞以及所有10个自发产生的抗性克隆都含有额外的4号染色体。讨论了4号染色体三体在DM-15细胞秋水仙碱抗性发展中的作用。