Raymond M, Rose E, Housman D E, Gros P
Department of Biochemistry, McGill University, Montreal, Quebec, Canada.
Mol Cell Biol. 1990 Apr;10(4):1642-51. doi: 10.1128/mcb.10.4.1642-1651.1990.
The mouse mdr gene family consists of three distinct genes (mdr1, mdr2, and mdr3), for which we have isolated full-length cDNA clones. cDNA subfragments corresponding to discrete regions showing little sequence conservation among the three mdr genes were used as gene-specific DNA probes in hybridization experiments. Long-range mapping by pulse-field gel electrophoresis indicated that the three mdr genes are closely linked on a genomic DNA segment of approximately 625 kilobases. The gene order and direction of transcription of the three genes were determined and indicate the arrangement (5') mdr3 (3')-(5') mdr1 (3')-(3') mdr2 (5'). Southern blotting analyses of genomic DNA from a panel of independently derived multidrug-resistant cell lines identified mdr gene amplification in 10 of 12 cell lines studied. In individual cell lines showing gene amplification, the copy number of each of the three mdr genes was identical, suggesting that the three mdr genes became amplified as part of a single amplicon in these cells. Although increased expression of all three mdr genes was detected in 2 of 12 cell lines tested, multidrug resistance was associated in 10 of 12 lines with the independent overexpression of either mdr1 (7 of 12) or mdr3 (3 of 12) but not mdr2. mdr1 overexpression was consistently associated with gene amplification, while increased mdr3 expression was detected in certain cell lines that did not show gene amplification. Increased levels of mdr1 mRNA were linked to the overexpression of a P glycoprotein of apparent molecular weight 180,000 to 200,000, whereas increased mdr3 expression resulted in increased expression of a P glycoprotein of molecular weight 160,000 to 180,000. Our results suggest that at least two members of the mouse mdr gene family, mdr1 and mdr3, can independently confer multidrug resistance in the cell lines examined.
小鼠多药耐药(mdr)基因家族由三个不同的基因(mdr1、mdr2和mdr3)组成,我们已分离出它们的全长cDNA克隆。对应于三个mdr基因之间序列保守性较低的离散区域的cDNA亚片段,在杂交实验中用作基因特异性DNA探针。通过脉冲场凝胶电泳进行的长距离定位表明,这三个mdr基因在大约625千碱基的基因组DNA片段上紧密相连。确定了这三个基因的基因顺序和转录方向,显示排列为(5')mdr3(3')-(5')mdr1(3')-(3')mdr2(5')。对一组独立衍生的多药耐药细胞系的基因组DNA进行的Southern印迹分析表明,在研究的12个细胞系中有10个出现了mdr基因扩增。在显示基因扩增的单个细胞系中,三个mdr基因中每个基因的拷贝数相同,这表明这三个mdr基因在这些细胞中作为单个扩增子的一部分被扩增。尽管在测试的12个细胞系中有2个检测到所有三个mdr基因的表达增加,但在12个细胞系中有10个的多药耐药与mdr1(12个中有7个)或mdr3(12个中有3个)的独立过表达相关,而与mdr2无关。mdr1过表达始终与基因扩增相关,而在某些未显示基因扩增的细胞系中检测到mdr3表达增加。mdr1 mRNA水平的升高与表观分子量为180,000至200,000的P糖蛋白的过表达有关,而mdr3表达的增加导致分子量为160,000至180,000的P糖蛋白表达增加。我们的结果表明,小鼠mdr基因家族的至少两个成员mdr1和mdr3可以在检测的细胞系中独立赋予多药耐药性。