Cantley L G, Zhou X M, Cunha M J, Epstein J, Cantley L C
Beth Israel Hospital, Harvard Medical School, Brigham and Women's Hospital, Boston, Massachusetts 02215.
J Biol Chem. 1992 Aug 25;267(24):17271-8.
A 6.5-kilobase murine genomic DNA fragment isolated by Levenson et al. (Levenson, R., Racaniello, V., Albritton, L., and Housman, D. (1984) Proc. Natl. Acad. Sci. U.S.A. 81, 1489-1493) (called the ouabain resistance gene) has been shown to produce ouabain resistance in primate cells. Preliminary sequence information has revealed no homology with the coding sequence of the Na,K-ATPase. We have introduced this murine sequence into monkey and murine cells in an attempt to characterize its mechanism of action. In our experiments, transfection of this DNA fragment is associated with the low frequency (1 in 8 x 10(5) cells) appearance of ouabain-resistant clones of CV1, COS, and NIH 3T3 cells, an event not seen in control transfections. Characterization of a new clone of ouabain-resistant CV1 cells (called OR8 cells) revealed a 5-fold increase in the IC50 for ouabain inhibition of rubidium uptake and a 10-fold increase in cell survival on ouabain. Although the murine sequence was detectable in Southern blots of ouabain-resistant cells soon after transfection, this exogenous DNA was rapidly lost despite continued exposure to ouabain. Furthermore, we were unable to detect message expression by this genomic sequence in any of the three cell types tested. Instead, we found that all three ouabain-resistant cell lines exhibited point mutations in a domain of the alpha-subunit that has been implicated in ouabain sensitivity (H1-H2). One of these mutations (Asp121-Asn121 in OR8 cells) has been previously reported to cause ouabain resistance (Price, E.M., Rice, D.A., and Lingrel, J.B. (1989) J. Biol. Chem. 264, 21902-21906). Other novel mutations in the H2 transmembrane domain were also detected. We postulate that the "ouabain resistance gene" is important in the early selection process on ouabain but that the permanent ouabain-resistant phenotype is due to a stable mutation in one allele of the alpha-subunit of the Na,K-ATPase.
莱文森等人(莱文森,R.,拉卡尼洛,V.,阿尔布里顿,L.,和豪斯曼,D.(1984年)《美国国家科学院院刊》81,1489 - 1493)分离出的一个6.5千碱基的小鼠基因组DNA片段(称为哇巴因抗性基因)已被证明能在灵长类细胞中产生对哇巴因的抗性。初步的序列信息显示它与钠钾ATP酶的编码序列没有同源性。我们已将这个小鼠序列导入猴细胞和小鼠细胞,试图阐明其作用机制。在我们的实验中,转染这个DNA片段与CV1、COS和NIH 3T3细胞中低频(8×10⁵个细胞中有1个)出现对哇巴因抗性的克隆有关,而在对照转染中未观察到这种情况。对一个新的对哇巴因抗性的CV1细胞克隆(称为OR8细胞)的特性分析显示,哇巴因抑制铷摄取的IC50增加了5倍,并且在哇巴因存在时细胞存活率增加了10倍。尽管在转染后不久在对哇巴因抗性细胞的Southern印迹中可检测到小鼠序列,但尽管持续暴露于哇巴因,这种外源DNA仍迅速丢失。此外,我们在测试的三种细胞类型中的任何一种中都未能检测到该基因组序列的信使RNA表达。相反,我们发现所有三种对哇巴因抗性的细胞系在α亚基的一个与哇巴因敏感性有关的结构域(H1 - H2)中都表现出点突变。这些突变之一(OR8细胞中的Asp121 - Asn121)先前已被报道会导致对哇巴因的抗性(普赖斯,E.M.,赖斯,D.A.,和林格雷尔,J.B.(1989年)《生物化学杂志》264,21902 - 21906)。在H2跨膜结构域中还检测到了其他新的突变。我们推测“哇巴因抗性基因”在哇巴因的早期选择过程中很重要,但永久性的哇巴因抗性表型是由于钠钾ATP酶α亚基的一个等位基因中的稳定突变所致。