细胞色素P-450基因及其调控。

M Adesnik, M Atchison
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引用次数: 199

摘要

肝微粒体混合功能氧化酶系统代谢多种外源性和内源性化合物的能力反映了多种形式的末端氧化酶细胞色素P-450的参与,它们具有不同的广泛但重叠的底物特异性。在动物暴露于特定的诱导剂后,这些同工酶中的一些在肝脏中积累。本文描述了近年来利用重组DNA技术研究各种细胞色素P-450同工酶的遗传和进化关系以及诱导现象的分子基础。从这些调查中得出的结论是在大量数据的背景下提出的,这些数据来自于特定细胞色素P-450同工酶的表征,以及在动物发育期间或用各种诱导剂治疗后对特定同工酶或酶活性的诱导研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genes for cytochrome P-450 and their regulation.

The capacity of the liver microsomal mixed-function oxidase system to metabolize a wide variety of exogenous as well as endogenous compounds reflects the participation of multiple forms of the terminal oxidase, cytochrome P-450, which have different broad, but overlapping, substrate specificities. Several of these isozymes accumulate in the liver after exposure of animals to specific inducing agents. Recent studies employing recombinant DNA techniques to investigate the genetic and evolutionary relatedness of various cytochrome P-450 isozymes as well as the molecular basis for the induction phenomenon are described. The conclusions from these investigations are presented in the context of the substantial body of data obtained from the characterization of specific cytochrome P-450 isozymes and from studies on the induction of specific isozymes or enzymatic activities during development or after treatment of animals with various inducing agents.

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