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活性氧诱导人类氧化碱基特异性DNA糖基化酶NEIL1的产生。

Induction of the human oxidized base-specific DNA glycosylase NEIL1 by reactive oxygen species.

作者信息

Das Aditi, Hazra Tapas K, Boldogh Istvan, Mitra Sankar, Bhakat Kishor K

机构信息

Sealy Center for Molecular Science and Department of Human Biological Chemistry and Genetics, University of Texas Medical Branch, Galveston 77555, USA.

出版信息

J Biol Chem. 2005 Oct 21;280(42):35272-80. doi: 10.1074/jbc.M505526200. Epub 2005 Aug 22.

Abstract

NEIL1, a mammalian DNA glycosylase and ortholog of Escherichia coli Nei/Fpg, is involved in the repair of oxidatively damaged bases in mammalian cells. Exposure of HCT116 human colon carcinoma cells to reactive oxygen species, generated by glucose oxidase (GO), enhanced the levels of NEIL1 mRNA and polypeptide by 2-4-fold by 6 h after GO treatment. A similar oxidative stress-induced increase in human NEIL1 (hNEIL1) promoter-dependent luciferase expression in HCT116 cells indicates that reactive oxygen species activates NEIL1 transcription. The transcriptional start site of hNEIL1 was mapped, and the upstream promoter sequence was characterized via luciferase reporter assay. Two identical CRE/AP-1-binding sites were identified in the promoter that binds transcription factors c-Jun and CREB/ATF2. This binding was significantly enhanced in extracts of cells treated with GO. Furthermore, a simultaneous increase in the level of phosphorylated c-Jun suggests its involvement in up-regulating the NEIL1 promoter. Oxidative stress-induced activation of NEIL1 appears to be involved in the feedback regulation of cellular repair activity needed to handle an increase in the level of oxidative base damage.

摘要

NEIL1是一种哺乳动物DNA糖基化酶,是大肠杆菌Nei/Fpg的直系同源物,参与哺乳动物细胞中氧化损伤碱基的修复。将HCT116人结肠癌细胞暴露于葡萄糖氧化酶(GO)产生的活性氧中,在GO处理后6小时,NEIL1 mRNA和多肽水平提高了2至4倍。在HCT116细胞中,类似的氧化应激诱导的人NEIL1(hNEIL1)启动子依赖性荧光素酶表达增加表明活性氧激活了NEIL1转录。绘制了hNEIL1的转录起始位点,并通过荧光素酶报告基因测定对上游启动子序列进行了表征。在启动子中鉴定出两个相同的CRE/AP-1结合位点,它们与转录因子c-Jun和CREB/ATF2结合。在用GO处理的细胞提取物中,这种结合显著增强。此外,磷酸化c-Jun水平的同时增加表明其参与上调NEIL1启动子。氧化应激诱导的NEIL1激活似乎参与了处理氧化碱基损伤水平增加所需的细胞修复活性的反馈调节。

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