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一氧化氮诱导的 S-亚硝化导致碱基切除修复失衡。

Nitric oxide induced S-nitrosation causes base excision repair imbalance.

机构信息

Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA; Center for Environmental Health Sciences, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.

Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA; Center for Environmental Health Sciences, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA; Department of Chemistry, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.

出版信息

DNA Repair (Amst). 2018 Aug;68:25-33. doi: 10.1016/j.dnarep.2018.04.008. Epub 2018 May 5.

Abstract

It is well established that inflammation leads to the creation of potent DNA damaging chemicals, including reactive oxygen and nitrogen species. Nitric oxide can react with glutathione to create S-nitrosoglutathione (GSNO), which can in turn lead to S-nitrosated proteins. Of particular interest is the impact of GSNO on the function of DNA repair enzymes. The base excision repair (BER) pathway can be initiated by the alkyl-adenine DNA glycosylase (AAG), a monofunctional glycosylase that removes methylated bases. After base removal, an abasic site is formed, which then gets cleaved by AP endonuclease and processed by downstream BER enzymes. Interestingly, using the Fluorescence-based Multiplexed Host Cell Reactivation Assay (FM-HCR), we show that GSNO actually enhances AAG activity, which is consistent with the literature. This raised the possibility that there might be imbalanced BER when cells are challenged with a methylating agent. To further explore this possibility, we confirmed that GSNO can cause AP endonuclease to translocate from the nucleus to the cytoplasm, which might further exacerbate imbalanced BER by increasing the levels of AP sites. Analysis of abasic sites indeed shows GSNO induces an increase in the level of AP sites. Furthermore, analysis of DNA damage using the CometChip (a higher throughput version of the comet assay) shows an increase in the levels of BER intermediates. Finally, we found that GSNO exposure is associated with an increase in methylation-induced cytotoxicity. Taken together, these studies support a model wherein GSNO increases BER initiation while processing of AP sites is decreased, leading to a toxic increase in BER intermediates. This model is also supported by additional studies performed in our laboratory showing that inflammation in vivo leads to increased large-scale sequence rearrangements. Taken together, this work provides new evidence that inflammatory chemicals can drive cytotoxicity and mutagenesis via BER imbalance.

摘要

众所周知,炎症会导致产生强效的 DNA 损伤化学物质,包括活性氧和氮物种。一氧化氮可以与谷胱甘肽反应生成 S-亚硝基谷胱甘肽(GSNO),GSNO 又可以导致 S-亚硝基化蛋白。特别有趣的是 GSNO 对 DNA 修复酶功能的影响。碱基切除修复(BER)途径可以由单功能糖苷酶烷基腺嘌呤 DNA 糖苷酶(AAG)启动,该酶去除甲基化碱基。碱基去除后,会形成无碱基位点,然后由 AP 内切核酸酶切割,并由下游 BER 酶处理。有趣的是,使用基于荧光的多重宿主细胞复活测定法(FM-HCR),我们发现 GSNO 实际上增强了 AAG 活性,这与文献一致。这提出了一种可能性,即在细胞受到甲基化剂挑战时,BER 可能会失衡。为了进一步探索这种可能性,我们证实 GSNO 可以使 AP 内切核酸酶从核转移到细胞质,这可能通过增加 AP 位点的水平进一步加剧 BER 失衡。碱基缺失分析确实表明 GSNO 诱导 AP 位点水平增加。此外,使用彗星芯片(彗星测定的高通量版本)分析 DNA 损伤显示 BER 中间产物水平增加。最后,我们发现 GSNO 暴露与甲基化诱导的细胞毒性增加有关。总之,这些研究支持了这样一种模型,即 GSNO 增加了 BER 的起始,同时减少了 AP 位点的处理,导致 BER 中间产物毒性增加。我们实验室进行的其他研究也支持了这一模型,表明体内炎症会导致大规模序列重排增加。总之,这项工作提供了新的证据,表明炎症化学物质可以通过 BER 失衡导致细胞毒性和突变。

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本文引用的文献

1
In vivo measurements of interindividual differences in DNA glycosylases and APE1 activities.
Proc Natl Acad Sci U S A. 2017 Nov 28;114(48):E10379-E10388. doi: 10.1073/pnas.1712032114. Epub 2017 Nov 9.
3
Parp1 protects against Aag-dependent alkylation-induced nephrotoxicity in a sex-dependent manner.
Oncotarget. 2016 Jul 19;7(29):44950-44965. doi: 10.18632/oncotarget.10440.
4
Evidence for Retromutagenesis as a Mechanism for Adaptive Mutation in Escherichia coli.
PLoS Genet. 2015 Aug 25;11(8):e1005477. doi: 10.1371/journal.pgen.1005477. eCollection 2015 Aug.
5
Micropatterned comet assay enables high throughput and sensitive DNA damage quantification.
Mutagenesis. 2015 Jan;30(1):11-9. doi: 10.1093/mutage/geu063.
7
DNA glycosylase activity and cell proliferation are key factors in modulating homologous recombination in vivo.
Carcinogenesis. 2014 Nov;35(11):2495-502. doi: 10.1093/carcin/bgu177. Epub 2014 Aug 25.
8
9
Multiplexed DNA repair assays for multiple lesions and multiple doses via transcription inhibition and transcriptional mutagenesis.
Proc Natl Acad Sci U S A. 2014 May 6;111(18):E1823-32. doi: 10.1073/pnas.1401182111. Epub 2014 Apr 22.
10
Chemistry meets biology in colitis-associated carcinogenesis.
Free Radic Res. 2013 Nov;47(11):958-86. doi: 10.3109/10715762.2013.832239. Epub 2013 Oct 4.

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