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对强心苷耐药的人类细胞突变体中不存在基因扩增现象。

Absence of gene amplification in human cell mutants resistant to cardiac glycosides.

作者信息

Dudani A K, Gupta R S

机构信息

Department of Biochemistry, McMaster University, Hamilton, Ontario, Canada.

出版信息

Mol Cell Biochem. 1987 Nov;78(1):73-9. doi: 10.1007/BF00224426.

Abstract

In HeLa cells, four different types of mutants resistant to cardiac glycosides viz. ouabain and SC4453, which differ from each other in cross resistance pattern, have been isolated after single-step selections [J Biol Chem 260 (1985) 6843-6850; J Biol Chem 261 (1986) 2034-2040]. Using cloned cDNA probes specific for the alpha and beta subunits of Na+/K+ ATPase, these mutants have been investigated for amplification and/or increased transcription of Na+/K+ ATPase genes. Results from dot blots, Southern and Northern hybridizations provide evidence that these mutants do not involve any amplification or increased transcription or gross structural alterations in Na+/K+ ATPase genes of their transcripts. Similar results were obtained with the mutant cells grown either in the absence or presence of cardiac glycosides, the latter conditions of which cause 3-4-fold increase in the resistant form of the enzyme within the mutant cells. These results are consistent with the inference that resistance to cardiac glycosides in these mutants may be due to specific point mutations within the structural gene(s) of Na+/K+ ATPase leading to an altered enzyme that is resistant to inhibition by different cardiac glycosides.

摘要

在HeLa细胞中,通过单步筛选分离出了四种不同类型的对强心苷(哇巴因和SC4453)具有抗性的突变体,它们在交叉抗性模式上彼此不同[《生物化学杂志》260 (1985) 6843 - 6850;《生物化学杂志》261 (1986) 2034 - 2040]。使用针对Na⁺/K⁺ ATP酶α和β亚基的克隆cDNA探针,对这些突变体进行了Na⁺/K⁺ ATP酶基因扩增和/或转录增加的研究。斑点印迹、Southern和Northern杂交的结果表明,这些突变体在其转录本的Na⁺/K⁺ ATP酶基因中不涉及任何扩增、转录增加或总体结构改变。在不存在或存在强心苷的情况下培养的突变细胞也得到了类似的结果,后者会使突变细胞内该酶的抗性形式增加3 - 4倍。这些结果与以下推断一致:这些突变体对强心苷的抗性可能是由于Na⁺/K⁺ ATP酶结构基因内的特定点突变,导致酶发生改变,从而对不同强心苷的抑制产生抗性。

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