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用于控制谷胱甘肽合成的谷氨酸半胱氨酸连接酶(GCL)转基因小鼠和基因靶向小鼠。

Glutamate cysteine ligase (GCL) transgenic and gene-targeted mice for controlling glutathione synthesis.

作者信息

Mohar Isaac, Botta Dianne, White Collin C, McConnachie Lisa A, Kavanagh Terrance J

机构信息

University of Washington, Seattle, Washington, USA.

出版信息

Curr Protoc Toxicol. 2009 Feb;Chapter 6:Unit6.16. doi: 10.1002/0471140856.tx0616s39.

Abstract

The tripeptide glutathione (GSH) has important antioxidant properties, scavenges free radicals, and serves as a cofactor for glutathione S-transferase conjugation of many xenobiotics. GSH is synthesized in two steps. The first and, often, rate-limiting step is the formation of γ-glutamylcysteine, which is catalyzed by the inducible heterodimeric enzyme glutamate cysteine ligase (GCL). The two subunits of GCL are the catalytic subunit (GCLC) and the modifier subunit (GCLM). In this unit, the generation and basic characterization methodologies of transgenic mouse models that have been developed to (1) conditionally over express both GCL subunits; (2) lack GCLM (Gclm null); and (3) create a hybrid between Gclm conditional over-expressing mice on a Gclm null genetic background are discussed. These models can be used to explore the fundamental role of GCLC and GCLM in GSH synthesis, as well as the toxicological role of GSH and its synthesis in xenobiotic metabolism and response to oxidative stress.

摘要

三肽谷胱甘肽(GSH)具有重要的抗氧化特性,能清除自由基,并作为谷胱甘肽S-转移酶与许多外源性物质结合的辅因子。GSH的合成分两步进行。第一步且通常是限速步骤是γ-谷氨酰半胱氨酸的形成,这由可诱导的异二聚体酶谷氨酸半胱氨酸连接酶(GCL)催化。GCL的两个亚基是催化亚基(GCLC)和调节亚基(GCLM)。在本单元中,将讨论已开发出的转基因小鼠模型的生成及基本表征方法,这些模型用于:(1)条件性过表达GCL的两个亚基;(2)缺乏GCLM(Gclm基因敲除);(3)在Gclm基因敲除的遗传背景上创建Gclm条件性过表达小鼠的杂交种。这些模型可用于探究GCLC和GCLM在GSH合成中的基本作用,以及GSH及其合成在异源物质代谢和氧化应激反应中的毒理学作用。

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