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3-羟基-3-甲基戊二酰辅酶A还原酶表达调控的体细胞遗传学分析

Somatic cell genetic analysis of regulation of expression of 3-hydroxy-3-methylglutaryl-coenzyme A reductase.

作者信息

Sinensky M, Armagast S, Mueller G, Torget R

出版信息

Proc Natl Acad Sci U S A. 1980 Nov;77(11):6621-3. doi: 10.1073/pnas.77.11.6621.

Abstract

Three new types of regulatory somatic cell mutants defective in expression of the enzyme 3-hydroxy-3-methylglutaryl coenzyme A reductase are described. They include a recessive mutant with abnormally high enzyme activity, apparently defective in degradation of the enzyme, and one, phenotypically a mevalonate auxotroph, that maintains permanently repressed levels of enzyme activity and are recessive, constitutive mutants. These mutants offer means for analyses of the mechanism of regulation of expression of 3-hydroxy-3-methylglutaryl coenzyme A reductase in cultured fibroblasts.

摘要

本文描述了三种新型的调节性体细胞突变体,这些突变体在3-羟基-3-甲基戊二酰辅酶A还原酶的表达方面存在缺陷。它们包括一种隐性突变体,其酶活性异常高,显然在酶的降解方面存在缺陷;还有一种表型为甲羟戊酸营养缺陷型的突变体,它能使酶活性水平永久处于被抑制状态,并且是隐性组成型突变体。这些突变体为分析培养的成纤维细胞中3-羟基-3-甲基戊二酰辅酶A还原酶的表达调控机制提供了手段。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eeb/350338/6af8d42e5fe2/pnas00498-0375-a.jpg

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