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基因表达调控中的亚硝化作用与氧化作用。

Nitrosation and oxidation in the regulation of gene expression.

作者信息

Marshall H E, Merchant K, Stamler J S

机构信息

Howard Hughes Medical Institute, Departments of Medicine and Biochemistry, Duke University Medical Center, Durham, North Carolina 27710, USA.

出版信息

FASEB J. 2000 Oct;14(13):1889-900. doi: 10.1096/fj.00.011rev.

Abstract

A growing body of evidence suggests that the cellular response to oxidative and nitrosative stress is primarily regulated at the level of transcription. Posttranslational modification of transcription factors may provide a mechanism by which cells sense these redox changes. In bacteria, for example, OxyR senses redox-related changes via oxidation or nitrosylation of a free thiol in the DNA binding region. This mode of regulation may serve as a paradigm for redox-sensing by eukaryotic transcription factors as most-including NF-kappaB, AP-1, and p53-contain reactive thiols in their DNA binding regions, the modification of which alters binding in vitro. Several of these transcription factors have been found to be sensitive to both reactive oxygen species and nitric oxide-related species in vivo. It remains entirely unclear, however, if oxidation or nitrosylation of eukaryotic transcription factors is an important mode of regulation, or whether transcriptional activating pathways are principally controlled at other redox-sensitive levels.-Marshall, H. E., Merchant, K., Stamler, J. S. Nitrosation and oxidation in the regulation of gene expression.

摘要

越来越多的证据表明,细胞对氧化应激和亚硝化应激的反应主要在转录水平上受到调控。转录因子的翻译后修饰可能提供了一种细胞感知这些氧化还原变化的机制。例如,在细菌中,OxyR通过DNA结合区域中游离硫醇的氧化或亚硝化来感知氧化还原相关变化。这种调节模式可能作为真核转录因子氧化还原感应的范例,因为大多数转录因子——包括核因子κB、激活蛋白-1和p53——在其DNA结合区域含有反应性硫醇,其修饰会在体外改变结合。已发现其中几种转录因子在体内对活性氧和一氧化氮相关物质均敏感。然而,真核转录因子的氧化或亚硝化是否是一种重要的调节模式,或者转录激活途径是否主要在其他氧化还原敏感水平上受到控制,目前仍完全不清楚。——马歇尔,H.E.,默chant,K.,斯塔姆勒,J.S. 基因表达调控中的亚硝化和氧化。

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