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利用绿色荧光蛋白对氧化应激调节子进行定量和动力学研究。

Quantitative and kinetic study of oxidative stress regulons using green fluorescent protein.

作者信息

Lu Canghai, Albano C Renee, Bentley William E, Rao Govind

机构信息

Department of Chemical and Biochemical Engineering, University of Maryland Baltimore County, 1000 Hilltop Circle, Baltimore, Maryland 21250, USA.

出版信息

Biotechnol Bioeng. 2005 Mar 5;89(5):574-87. doi: 10.1002/bit.20389.

Abstract

Potentially damaging reactive oxygen species (ROS) are involved in a number of pathways ranging from signal transduction to apoptosis. Cells have adapted this alteration in redox status into a complex regulatory mechanism. ROS are specifically able to induce the expression of a multitude of genes. We constructed and characterized "oxidative stress probes" consisting of promoter fusions of several ROS-induced genes and the green fluorescent protein (GFP) reporter gene. Specifically, the sodA, fumC, zwf, acnA, acrAB, and soxS genes from the SoxRS regulon and the katG and ahpC genes from OxyR regulon, which respond to the superoxide anion and hydrogen peroxide, were studied. Our results revealed not only different levels of background transcription, but different induction levels both in terms of timing and strength. These systematic studies were performed under a uniform parallel platform and have provided insight into the complicated gene regulation of the oxidative stress regulons.

摘要

具有潜在破坏性的活性氧(ROS)参与了从信号转导到细胞凋亡等多种途径。细胞已将这种氧化还原状态的改变调整为一种复杂的调节机制。ROS能够特异性地诱导众多基因的表达。我们构建并表征了“氧化应激探针”,其由几个ROS诱导基因的启动子融合体和绿色荧光蛋白(GFP)报告基因组成。具体而言,研究了来自SoxRS调节子的sodA、fumC、zwf、acnA、acrAB和soxS基因以及来自OxyR调节子的katG和ahpC基因,它们对超氧阴离子和过氧化氢有反应。我们的结果不仅揭示了不同水平的背景转录,还揭示了在时间和强度方面不同的诱导水平。这些系统研究是在统一的平行平台上进行的,为深入了解氧化应激调节子的复杂基因调控提供了依据。

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