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环境电外源性化学物质通过抑制 DNA 甲基转移酶调节 CXCL 趋化因子的表达的表观遗传调控作用。

Epigenetic Regulation of CXC Chemokine Expression by Environmental Electrophiles Through DNA Methyltransferase Inhibition.

机构信息

Department of Medicinal Pharmacology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama 700-8530, Japan.

Department of Medicinal Pharmacology, Faculty of Pharmaceutical Sciences, Okayama University, Okayama 700-8530, Japan.

出版信息

Int J Mol Sci. 2024 Oct 29;25(21):11592. doi: 10.3390/ijms252111592.


DOI:10.3390/ijms252111592
PMID:39519144
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11546359/
Abstract

Ubiquitously distributed environmental electrophiles covalently modify DNA and proteins, potentially leading to adverse health effects. However, the impacts of specific electrophiles on target proteins and their physiological roles remain largely unknown. In the present study, we focused on DNA methylation, which regulates gene expression and physiological responses. A total of 45 environmental electrophiles were screened for inhibitory effects on the activity of DNA methyltransferase 3B (DNMT3B), a key enzyme in DNA methylation, and four compounds were identified. We focused on 1,2-naphthoquinone (1,2-NQ), an air pollutant whose toxicity has been reported previously. Interestingly, we found that 1,2-NQ modified multiple lysine and histidine residues in DNMT3B, one of which was near the active site in DNMT3B. It was found that 1,2-NQ altered gene expression and evoked inflammatory responses in lung adenocarcinoma cell lines. Furthermore, we found that 1,2-NQ upregulated expression through DNA demethylation of the distal enhancer and promoted cancer cell growth. Our study reveals novel mechanisms of epigenetic regulation by environmental electrophiles through the inhibition of DNMT3B activity and suggests their physiological impact.

摘要

无处不在的环境亲电试剂会使 DNA 和蛋白质发生共价修饰,从而可能导致不良的健康影响。然而,特定的亲电试剂对靶蛋白的影响及其生理作用在很大程度上仍然未知。在本研究中,我们重点研究了 DNA 甲基化,它调节基因表达和生理反应。总共筛选了 45 种环境亲电试剂,以抑制 DNA 甲基转移酶 3B(DNMT3B)的活性,DNMT3B 是 DNA 甲基化的关键酶,发现其中四种化合物具有抑制作用。我们重点研究了 1,2-萘醌(1,2-NQ),它是一种空气污染物,其毒性以前已有报道。有趣的是,我们发现 1,2-NQ 修饰了 DNMT3B 中的多个赖氨酸和组氨酸残基,其中一个残基位于 DNMT3B 的活性部位附近。结果表明,1,2-NQ 通过改变肺腺癌细胞系中的基因表达并引发炎症反应。此外,我们发现 1,2-NQ 通过远端增强子的 DNA 去甲基化而上调 的表达,促进癌细胞生长。我们的研究揭示了环境亲电试剂通过抑制 DNMT3B 活性来调节表观遗传的新机制,并提示了它们的生理影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7613/11546359/d6816aa268a5/ijms-25-11592-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7613/11546359/427e29a212dc/ijms-25-11592-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7613/11546359/94007a4529cf/ijms-25-11592-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7613/11546359/1ff02ad08029/ijms-25-11592-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7613/11546359/9af964c9a51e/ijms-25-11592-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7613/11546359/2dba718e47ba/ijms-25-11592-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7613/11546359/f4b3bee4b365/ijms-25-11592-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7613/11546359/819e898b76cd/ijms-25-11592-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7613/11546359/d6816aa268a5/ijms-25-11592-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7613/11546359/427e29a212dc/ijms-25-11592-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7613/11546359/94007a4529cf/ijms-25-11592-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7613/11546359/1ff02ad08029/ijms-25-11592-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7613/11546359/9af964c9a51e/ijms-25-11592-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7613/11546359/2dba718e47ba/ijms-25-11592-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7613/11546359/f4b3bee4b365/ijms-25-11592-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7613/11546359/819e898b76cd/ijms-25-11592-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7613/11546359/d6816aa268a5/ijms-25-11592-g008.jpg

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Epigenetic Regulation of CXC Chemokine Expression by Environmental Electrophiles Through DNA Methyltransferase Inhibition.

Int J Mol Sci. 2024-10-29

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[1]
Tobacco-induced hyperglycemia promotes lung cancer progression via cancer cell-macrophage interaction through paracrine IGF2/IR/NPM1-driven PD-L1 expression.

Nat Commun. 2024-6-8

[2]
Chromatin modifier Hmga2 promotes adult hematopoietic stem cell function and blood regeneration in stress conditions.

EMBO J. 2024-7

[3]
The EMBL-EBI Job Dispatcher sequence analysis tools framework in 2024.

Nucleic Acids Res. 2024-7-5

[4]
Nuclear SphK2/S1P signaling is a key regulator of ApoE production and Aβ uptake in astrocytes.

J Lipid Res. 2024-3

[5]
Methyl vinyl ketone and its analogs covalently modify PI3K and alter physiological functions by inhibiting PI3K signaling.

J Biol Chem. 2024-3

[6]
Structural basis for the allosteric regulation and dynamic assembly of DNMT3B.

Nucleic Acids Res. 2023-12-11

[7]
Analysis and Visualization of Longitudinal Genomic and Clinical Data from the AACR Project GENIE Biopharma Collaborative in cBioPortal.

Cancer Res. 2023-12-1

[8]
The role of CXCL family members in different diseases.

Cell Death Discov. 2023-7-1

[9]
Relevance of DNA methylation at enhancers for the acquisition of cell identities.

FEBS Lett. 2023-7

[10]
PM2.5 promotes lung cancer progression through activation of the AhR-TMPRSS2-IL18 pathway.

EMBO Mol Med. 2023-6-7

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