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用编码大鼠钠钾ATP酶α1亚基的cDNA转染CV-1细胞后,哇巴因抗性钠钾ATP酶的表达。

Expression of an ouabain-resistant Na,K-ATPase in CV-1 cells after transfection with a cDNA encoding the rat Na,K-ATPase alpha 1 subunit.

作者信息

Emanuel J R, Schulz J, Zhou X M, Kent R B, Housman D, Cantley L, Levenson R

机构信息

Department of Cell Biology, Yale University School of Medicine, New Haven, Connecticut 06510.

出版信息

J Biol Chem. 1988 Jun 5;263(16):7726-33.

PMID:2836394
Abstract

We have used a gene transfer system to investigate the relationship between expression of the rat Na,K-ATPase alpha 1 subunit gene and ouabain-resistant Na,K-ATPase activity. A cDNA clone encoding the entire rat Na,K-ATPase alpha 1 subunit was inserted into the expression vector pSV2neo. This construct (pSV2 alpha 1) conferred resistance to 100 microM ouabain to ouabain-sensitive CV-1 cells. Hybridization analysis of transfected clones revealed the presence of both rat-specific and endogenous Na,K-ATPase alpha 1 subunit DNA and mRNA sequences. A single form of highly ouabain-sensitive 86Rb+ uptake was detected in CV-1 cells, whereas two distinct classes of ouabain-inhibitable uptake were observed in transfectants. One class exhibited the high ouabain sensitivity of the endogenous monkey Na,K-ATPase, while the second class showed the reduced ouabain sensitivity characteristic of the rodent renal Na,K-ATPase. Examination of the ouabain-sensitive, sodium-dependent ATPase activity of the transfectants also revealed a low affinity component of Na,K-ATPase activity characteristic of the rodent kidney enzyme. These results suggest that expression of the rat alpha 1 subunit gene is directly responsible for ouabain-resistant Na,K-ATPase activity in transfected CV-1 cells.

摘要

我们使用了一种基因转移系统来研究大鼠钠钾ATP酶α1亚基基因的表达与哇巴因抗性钠钾ATP酶活性之间的关系。将编码完整大鼠钠钾ATP酶α1亚基的cDNA克隆插入表达载体pSV2neo中。该构建体(pSV2α1)赋予对哇巴因敏感的CV-1细胞对100μM哇巴因的抗性。对转染克隆的杂交分析显示存在大鼠特异性和内源性钠钾ATP酶α1亚基DNA及mRNA序列。在CV-1细胞中检测到单一形式的高度哇巴因敏感的86Rb +摄取,而在转染子中观察到两类不同的哇巴因抑制性摄取。一类表现出内源性猴钠钾ATP酶的高哇巴因敏感性,而另一类则表现出啮齿动物肾钠钾ATP酶特征性的降低的哇巴因敏感性。对转染子的哇巴因敏感的、钠依赖性ATP酶活性的检测还揭示了啮齿动物肾酶特征性的钠钾ATP酶活性的低亲和力成分。这些结果表明大鼠α1亚基基因的表达直接导致转染的CV-1细胞中出现哇巴因抗性钠钾ATP酶活性。

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