• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

四氢叶酸诱导的5-甲基胞嘧啶氧化产物对Dnmt1和DNMT3a介导的胞嘧啶甲基化的影响。

Effects of Tet-induced oxidation products of 5-methylcytosine on Dnmt1- and DNMT3a-mediated cytosine methylation.

作者信息

Ji Debin, Lin Krystal, Song Jikui, Wang Yinsheng

机构信息

Department of Chemistry, University of California, Riverside, CA 92521, USA.

出版信息

Mol Biosyst. 2014 Jul;10(7):1749-52. doi: 10.1039/c4mb00150h. Epub 2014 Apr 30.

DOI:10.1039/c4mb00150h
PMID:24789765
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4052722/
Abstract

We investigated systematically the effects of Tet-induced oxidation products of 5-methylcytosine on Dnmt1- and DNMT3a-mediated cytosine methylation in synthetic duplex DNA. We found that the replacement of 5-methylcytosine at a CpG site with a 5-hydroxymethylcytosine, 5-formylcytosine, 5-carboxylcytosine or 5-hydroxymethyluracil resulted in altered methylation of cytosine at both the opposite and the neighboring CpG sites. Our results provided important new knowledge about the implications of the 5-methylcytosine oxidation products in maintenance cytosine methylation.

摘要

我们系统地研究了四氢叶酸诱导的5-甲基胞嘧啶氧化产物对合成双链DNA中Dnmt1和DNMT3a介导的胞嘧啶甲基化的影响。我们发现,在CpG位点用5-羟甲基胞嘧啶、5-甲酰基胞嘧啶、5-羧基胞嘧啶或5-羟甲基尿嘧啶取代5-甲基胞嘧啶会导致相对和相邻CpG位点的胞嘧啶甲基化发生改变。我们的结果为5-甲基胞嘧啶氧化产物在维持胞嘧啶甲基化中的作用提供了重要的新知识。

相似文献

1
Effects of Tet-induced oxidation products of 5-methylcytosine on Dnmt1- and DNMT3a-mediated cytosine methylation.四氢叶酸诱导的5-甲基胞嘧啶氧化产物对Dnmt1和DNMT3a介导的胞嘧啶甲基化的影响。
Mol Biosyst. 2014 Jul;10(7):1749-52. doi: 10.1039/c4mb00150h. Epub 2014 Apr 30.
2
TET enzymatic oxidation of 5-methylcytosine, 5-hydroxymethylcytosine and 5-formylcytosine.5-甲基胞嘧啶、5-羟甲基胞嘧啶和5-甲酰基胞嘧啶的TET酶促氧化作用。
Mutat Res Genet Toxicol Environ Mutagen. 2014 Apr;764-765:18-35. doi: 10.1016/j.mrgentox.2013.09.001. Epub 2013 Sep 14.
3
Oxidized C5-methyl cytosine bases in DNA: 5-Hydroxymethylcytosine; 5-formylcytosine; and 5-carboxycytosine.DNA中的氧化C5-甲基胞嘧啶碱基:5-羟甲基胞嘧啶;5-甲酰基胞嘧啶;以及5-羧基胞嘧啶。
Free Radic Biol Med. 2017 Jun;107:62-68. doi: 10.1016/j.freeradbiomed.2016.11.038. Epub 2016 Nov 24.
4
The existence of 5-hydroxymethylcytosine and 5-formylcytosine in both DNA and RNA in mammals.5-羟甲基胞嘧啶和5-甲酰基胞嘧啶在哺乳动物的DNA和RNA中的存在。
Chem Commun (Camb). 2016 Jan 14;52(4):737-40. doi: 10.1039/c5cc07354e.
5
Maintenance DNA Methyltransferase Activity in the Presence of Oxidized Forms of 5-Methylcytosine: Structural Basis for Ten Eleven Translocation-Mediated DNA Demethylation.5-甲基胞嘧啶氧化形式存在时维持DNA甲基转移酶活性:十一易位介导的DNA去甲基化的结构基础
Biochemistry. 2018 Oct 23;57(42):6061-6069. doi: 10.1021/acs.biochem.8b00683. Epub 2018 Oct 8.
6
Tet proteins can convert 5-methylcytosine to 5-formylcytosine and 5-carboxylcytosine.Tet 蛋白可以将 5-甲基胞嘧啶转化为 5-醛基胞嘧啶和 5-羧基胞嘧啶。
Science. 2011 Sep 2;333(6047):1300-3. doi: 10.1126/science.1210597. Epub 2011 Jul 21.
7
Preferential 5-Methylcytosine Oxidation in the Linker Region of Reconstituted Positioned Nucleosomes by Tet1 Protein.Tet1 蛋白优先氧化组蛋白定位重构连接区的 5-甲基胞嘧啶。
Chemistry. 2016 Nov 7;22(46):16598-16601. doi: 10.1002/chem.201602435. Epub 2016 Sep 30.
8
5-hydroxymethylcytosine in cancer: significance in diagnosis and therapy.癌症中的5-羟甲基胞嘧啶:在诊断和治疗中的意义
Cancer Genet. 2015 May;208(5):167-77. doi: 10.1016/j.cancergen.2015.02.009. Epub 2015 Mar 3.
9
Vitamin C enhances substantially formation of 5-hydroxymethyluracil in cellular DNA.维生素C可显著增强细胞DNA中5-羟甲基尿嘧啶的形成。
Free Radic Biol Med. 2016 Dec;101:378-383. doi: 10.1016/j.freeradbiomed.2016.10.535. Epub 2016 Nov 8.
10
The hypomethylating agent Decitabine causes a paradoxical increase in 5-hydroxymethylcytosine in human leukemia cells.低甲基化剂地西他滨会导致人类白血病细胞中5-羟甲基胞嘧啶出现反常增加。
Sci Rep. 2015 Apr 22;5:9281. doi: 10.1038/srep09281.

引用本文的文献

1
TET1 functions as a tumor suppressor in lung adenocarcinoma through epigenetic remodeling and immune modulation.TET1通过表观遗传重塑和免疫调节在肺腺癌中发挥肿瘤抑制作用。
Epigenetics Chromatin. 2025 Aug 11;18(1):53. doi: 10.1186/s13072-025-00617-2.
2
From Lineage to Longevity: A Field Guide to the Key Players in Epigenetic Contribution to Offspring Health.从谱系到长寿:表观遗传学对后代健康影响的关键因素实用指南
Curr Issues Mol Biol. 2025 Apr 30;47(5):323. doi: 10.3390/cimb47050323.
3
5-hydroxymethylcytosines regulate gene expression as a passive DNA demethylation resisting epigenetic mark in proliferative somatic cells.5-羟甲基胞嘧啶作为一种抵抗表观遗传标记的被动DNA去甲基化方式,在增殖性体细胞中调节基因表达。
bioRxiv. 2023 Sep 27:2023.09.26.559662. doi: 10.1101/2023.09.26.559662.
4
TET (Ten-eleven translocation) family proteins: structure, biological functions and applications.TET(Ten-eleven translocation)家族蛋白:结构、生物学功能及应用。
Signal Transduct Target Ther. 2023 Aug 11;8(1):297. doi: 10.1038/s41392-023-01537-x.
5
On the accuracy of the epigenetic copy machine: comprehensive specificity analysis of the DNMT1 DNA methyltransferase.关于表观遗传复制机器的准确性:DNMT1 DNA 甲基转移酶的综合特异性分析。
Nucleic Acids Res. 2023 Jul 21;51(13):6622-6633. doi: 10.1093/nar/gkad465.
6
A View on Uterine Leiomyoma Genesis through the Prism of Genetic, Epigenetic and Cellular Heterogeneity.从遗传、表观遗传和细胞异质性的角度看子宫肌瘤的发生。
Int J Mol Sci. 2023 Mar 17;24(6):5752. doi: 10.3390/ijms24065752.
7
Mammalian DNA methylome dynamics: mechanisms, functions and new frontiers.哺乳动物 DNA 甲基组动态:机制、功能与新前沿。
Development. 2022 Dec 15;149(24). doi: 10.1242/dev.182683.
8
Epigenetic Therapeutics Targeting NRF2/KEAP1 Signaling in Cancer Oxidative Stress.针对癌症氧化应激中NRF2/KEAP1信号通路的表观遗传疗法
Front Pharmacol. 2022 Jun 9;13:924817. doi: 10.3389/fphar.2022.924817. eCollection 2022.
9
DNA Hydroxymethylation in Smoking-Associated Cancers.吸烟相关癌症中的 DNA 羟甲基化。
Int J Mol Sci. 2022 Feb 28;23(5):2657. doi: 10.3390/ijms23052657.
10
Direct and Base Excision Repair-Mediated Regulation of a GC-Rich -Element in Response to 5-Formylcytosine and 5-Carboxycytosine.直接修复和碱基切除修复介导的富含 GC 元件对 5-甲酰胞嘧啶和 5-羧基胞嘧啶的响应调控。
Int J Mol Sci. 2021 Oct 13;22(20):11025. doi: 10.3390/ijms222011025.

本文引用的文献

1
Nucleic acid oxidation in DNA damage repair and epigenetics.DNA损伤修复与表观遗传学中的核酸氧化
Chem Rev. 2014 Apr 23;114(8):4602-20. doi: 10.1021/cr400432d. Epub 2014 Feb 28.
2
Tandem mass spectrometry of small, multiply charged oligonucleotides.串联质谱法分析小的、多电荷寡核苷酸。
J Am Soc Mass Spectrom. 1992 Jan;3(1):60-70. doi: 10.1016/1044-0305(92)85019-G.
3
Potential functional roles of DNA demethylation intermediates.DNA 去甲基化中间产物的潜在功能作用。
Trends Biochem Sci. 2013 Oct;38(10):480-4. doi: 10.1016/j.tibs.2013.07.003. Epub 2013 Aug 8.
4
Quantitative assessment of Tet-induced oxidation products of 5-methylcytosine in cellular and tissue DNA.定量评估 Tet 诱导的细胞和组织 DNA 中 5-甲基胞嘧啶的氧化产物。
Nucleic Acids Res. 2013 Jul;41(13):6421-9. doi: 10.1093/nar/gkt360. Epub 2013 May 8.
5
5-Hydroxymethylcytosine: generation, fate, and genomic distribution.5-羟甲基胞嘧啶:生成、命运和基因组分布。
Curr Opin Cell Biol. 2013 Jun;25(3):289-96. doi: 10.1016/j.ceb.2013.02.017. Epub 2013 Mar 13.
6
CpG site-specific alteration of hydroxymethylcytosine to methylcytosine beyond DNA replication.CpG 位点特异性羟甲基胞嘧啶向甲基胞嘧啶的转化超越了 DNA 复制。
Biochem Biophys Res Commun. 2012 Sep 14;426(1):141-7. doi: 10.1016/j.bbrc.2012.08.053. Epub 2012 Aug 17.
7
Biochemical and structural characterization of the glycosylase domain of MBD4 bound to thymine and 5-hydroxymethyuracil-containing DNA.MBD4 糖苷酶结构域与胸腺嘧啶和 5-羟甲基尿嘧啶含 DNA 复合物的生化和结构特征。
Nucleic Acids Res. 2012 Oct;40(19):9917-26. doi: 10.1093/nar/gks714. Epub 2012 Jul 30.
8
Recognition and potential mechanisms for replication and erasure of cytosine hydroxymethylation.识别和潜在的机制,用于复制和消除胞嘧啶羟甲基化。
Nucleic Acids Res. 2012 Jun;40(11):4841-9. doi: 10.1093/nar/gks155. Epub 2012 Feb 22.
9
Thymine DNA glycosylase specifically recognizes 5-carboxylcytosine-modified DNA.胸腺嘧啶 DNA 糖基化酶特异性识别 5-羧基胞嘧啶修饰的 DNA。
Nat Chem Biol. 2012 Feb 12;8(4):328-30. doi: 10.1038/nchembio.914.
10
Structure-based mechanistic insights into DNMT1-mediated maintenance DNA methylation.基于结构的 DNMT1 介导的维持 DNA 甲基化的机制见解。
Science. 2012 Feb 10;335(6069):709-12. doi: 10.1126/science.1214453.