Buchwald M, Clarke C
Research Institute Hospital for Sick Children, Toronto, Ontario, Canada.
J Cell Physiol. 1991 Sep;148(3):472-8. doi: 10.1002/jcp.1041480320.
Attempts to complement the defect in the mitomycin C (MMC)-sensitive Chinese hamster ovary (CHO) mutant MMC3 led to the isolation of hybrids with high resistance to the cytotoxic action of the drug. Hybrid cells selected with MMC after fusion of MMC3 cells to human diploid fibroblasts were approximately five times more resistant to MMC than wild-type CHO cells but retained the original MMC3 sensitivity to another DNA cross-linking agent, diepoxybutane. To confirm that the MMC resistance was genetically determined and was of human origin, DNA from the resistant hybrids was introduced into MMC3 cells, and transfectants were selected in MMC. These cells had the same level of MMC resistance as the hybrids. Thus we have identified a human gene that can confer MMC resistance to CHO cells. Identification of the gene should help understand the mechanisms of MMC resistance in mammalian cells.
为了弥补对丝裂霉素C(MMC)敏感的中国仓鼠卵巢(CHO)突变体MMC3中的缺陷,人们进行了一系列尝试,最终成功分离出了对该药物的细胞毒性作用具有高度抗性的杂种细胞。将MMC3细胞与人二倍体成纤维细胞融合后,用MMC筛选出的杂种细胞对MMC的抗性大约是野生型CHO细胞的五倍,但对另一种DNA交联剂1,4 - 二环氧丁烷仍保留原来的MMC3敏感性。为了证实MMC抗性是由基因决定的且源自人类,将抗性杂种细胞的DNA导入MMC3细胞,并在MMC中筛选转染子。这些细胞具有与杂种细胞相同水平的MMC抗性。因此,我们鉴定出了一个能够赋予CHO细胞MMC抗性的人类基因。该基因的鉴定有助于理解哺乳动物细胞中MMC抗性的机制。