• 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

N6-甲基腺苷修饰乙型肝炎病毒 RNA 编码区。

N6-methyladenosine Modification of Hepatitis B Virus RNA in the Coding Region of .

机构信息

Department of Virology and Parasitology, Fujita Health University School of Medicine, Toyoake 470-1192, Japan.

Department of Virology, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan.

出版信息

Int J Mol Sci. 2023 Jan 23;24(3):2265. doi: 10.3390/ijms24032265.

DOI:10.3390/ijms24032265
PMID:36768585
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9917364/
Abstract

N6-methyladenosine (mA) is a post-transcriptional modification of RNA involved in transcript transport, degradation, translation, and splicing. We found that HBV RNA is modified by mA predominantly in the coding region of . The mutagenesis of methylation sites reduced the HBV mRNA and HBs protein levels. The suppression of mA by an inhibitor or knockdown in primary hepatocytes decreased the viral RNA and HBs protein levels in the medium. These results suggest that the mA modification of HBV RNA is needed for the efficient replication of HBV in hepatocytes.

摘要

N6-甲基腺苷(mA)是 RNA 的一种转录后修饰,参与转录物的运输、降解、翻译和剪接。我们发现,HBV RNA 主要在. 的编码区被 mA 修饰。甲基化位点的突变降低了 HBV mRNA 和 HBs 蛋白水平。在原代肝细胞中用抑制剂或敲低抑制 mA 可降低培养基中的病毒 RNA 和 HBs 蛋白水平。这些结果表明,HBV RNA 的 mA 修饰对于 HBV 在肝细胞中的有效复制是必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/462e/9917364/1f588c9db3af/ijms-24-02265-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/462e/9917364/e80c282e5037/ijms-24-02265-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/462e/9917364/6e4426e9b58e/ijms-24-02265-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/462e/9917364/e65c2218ba79/ijms-24-02265-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/462e/9917364/f88223de2d66/ijms-24-02265-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/462e/9917364/cc01afc46171/ijms-24-02265-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/462e/9917364/1f588c9db3af/ijms-24-02265-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/462e/9917364/e80c282e5037/ijms-24-02265-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/462e/9917364/6e4426e9b58e/ijms-24-02265-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/462e/9917364/e65c2218ba79/ijms-24-02265-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/462e/9917364/f88223de2d66/ijms-24-02265-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/462e/9917364/cc01afc46171/ijms-24-02265-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/462e/9917364/1f588c9db3af/ijms-24-02265-g006.jpg

相似文献

1
N6-methyladenosine Modification of Hepatitis B Virus RNA in the Coding Region of .N6-甲基腺苷修饰乙型肝炎病毒 RNA 编码区。
Int J Mol Sci. 2023 Jan 23;24(3):2265. doi: 10.3390/ijms24032265.
2
Hepatitis B Virus X Protein Expression Is Tightly Regulated by N6-Methyladenosine Modification of Its mRNA.乙型肝炎病毒 X 蛋白的表达受其 mRNA 的 N6-甲基腺苷修饰的严格调控。
J Virol. 2022 Feb 23;96(4):e0165521. doi: 10.1128/JVI.01655-21. Epub 2021 Dec 1.
3
Hepatitis B virus X protein recruits methyltransferases to affect cotranscriptional N6-methyladenosine modification of viral/host RNAs.乙型肝炎病毒 X 蛋白招募甲基转移酶来影响病毒/宿主 RNA 的共转录 N6-甲基腺苷修饰。
Proc Natl Acad Sci U S A. 2021 Jan 19;118(3). doi: 10.1073/pnas.2019455118.
4
Lost Small Envelope Protein Expression from Naturally Occurring PreS1 Deletion Mutants of Hepatitis B Virus Is Often Accompanied by Increased HBx and Core Protein Expression as Well as Genome Replication.自然发生的 PreS1 缺失突变乙型肝炎病毒的丢失小信封蛋白表达通常伴随着 HBx 和核心蛋白表达以及基因组复制的增加。
J Virol. 2021 Jun 24;95(14):e0066021. doi: 10.1128/JVI.00660-21.
5
Peroxiredoxin 1, a Novel HBx-Interacting Protein, Interacts with Exosome Component 5 and Negatively Regulates Hepatitis B Virus (HBV) Propagation through Degradation of HBV RNA.过氧化物酶 1,一种新型的 HBx 相互作用蛋白,与外泌体成分 5 相互作用,并通过降解 HBV RNA 负调控乙型肝炎病毒 (HBV) 的复制。
J Virol. 2019 Mar 5;93(6). doi: 10.1128/JVI.02203-18. Print 2019 Mar 15.
6
Type-III interferon stimulated gene TRIM31 mutation in an HBV patient blocks its ability in promoting HBx degradation.一名乙肝患者中III型干扰素刺激基因TRIM31的突变阻碍了其促进乙肝X蛋白(HBx)降解的能力。
Virus Res. 2022 Jan 15;308:198650. doi: 10.1016/j.virusres.2021.198650. Epub 2021 Dec 1.
7
The C-terminal region of the hepatitis B virus X protein is required for its stimulation of HBV replication in primary mouse hepatocytes.乙型肝炎病毒 X 蛋白的 C 末端区域对于其在原代小鼠肝细胞中刺激 HBV 复制是必需的。
Virus Res. 2012 May;165(2):170-8. doi: 10.1016/j.virusres.2012.02.013. Epub 2012 Feb 23.
8
Parvulin 14 and Parvulin 17 Bind to HBx and cccDNA and Upregulate Hepatitis B Virus Replication from cccDNA to Virion in an HBx-Dependent Manner.微小核核糖核蛋白 14 和微小核核糖核蛋白 17 与 HBx 和共价闭合环状 DNA 结合,并以 HBx 依赖的方式从共价闭合环状 DNA 上调乙型肝炎病毒复制至病毒粒子。
J Virol. 2019 Mar 5;93(6). doi: 10.1128/JVI.01840-18. Print 2019 Mar 15.
9
TRIM26 inhibits hepatitis B virus replication by promoting HBx degradation and TRIM26 genetic polymorphism predicts PegIFNα treatment response of HBeAg-positive chronic hepatitis B Patients.TRIM26 通过促进 HBx 降解来抑制乙型肝炎病毒复制,TRIM26 基因多态性可预测 HBeAg 阳性慢性乙型肝炎患者对 PegIFNα 治疗的反应。
Aliment Pharmacol Ther. 2022 Sep;56(5):878-889. doi: 10.1111/apt.17124. Epub 2022 Jul 24.
10
Cellular UAP56 interacts with the HBx protein of the hepatitis B virus and is involved in viral RNA nuclear export in hepatocytes.细胞 UAP56 与乙型肝炎病毒的 HBx 蛋白相互作用,并参与肝细胞中病毒 RNA 的核输出。
Exp Cell Res. 2020 May 1;390(1):111929. doi: 10.1016/j.yexcr.2020.111929. Epub 2020 Mar 10.

引用本文的文献

1
Targeting m6A methylation for early diagnosis and precision medicine in hepatocellular carcinoma.靶向m6A甲基化用于肝细胞癌的早期诊断和精准医学
Cancer Cell Int. 2025 Jul 28;25(1):286. doi: 10.1186/s12935-025-03923-7.
2
Role of N6-methyladenosine RNA modification in cancer.N6-甲基腺苷RNA修饰在癌症中的作用。
MedComm (2020). 2024 Sep 9;5(9):e715. doi: 10.1002/mco2.715. eCollection 2024 Sep.
3
The Interactions between Cells and Viruses.细胞与病毒的相互作用。

本文引用的文献

1
EBV Exploits RNA mA Modification to Promote Cell Survival and Progeny Virus Production During Lytic Cycle.EB病毒利用RNA mA修饰在裂解周期中促进细胞存活和子代病毒产生。
Front Microbiol. 2022 Jun 15;13:870816. doi: 10.3389/fmicb.2022.870816. eCollection 2022.
2
m A RNA methylation: from mechanisms to therapeutic potential.mRNA 甲基化:从机制到治疗潜力。
EMBO J. 2021 Feb 1;40(3):e105977. doi: 10.15252/embj.2020105977. Epub 2021 Jan 20.
3
Biological functions of mA methyltransferases.mA甲基转移酶的生物学功能。
Int J Mol Sci. 2024 Jun 23;25(13):6886. doi: 10.3390/ijms25136886.
4
Recent insights into N-methyladenosine during viral infection.病毒感染中 N6-甲基腺苷的最新研究进展。
Curr Opin Genet Dev. 2024 Aug;87:102213. doi: 10.1016/j.gde.2024.102213. Epub 2024 Jun 19.
5
Epitranscriptomic cytidine methylation of the hepatitis B viral RNA is essential for viral reverse transcription and particle production.乙型肝炎病毒 RNA 的转录后胞嘧啶甲基化对于病毒的逆转录和颗粒生成至关重要。
Proc Natl Acad Sci U S A. 2024 Jun 11;121(24):e2400378121. doi: 10.1073/pnas.2400378121. Epub 2024 Jun 3.
6
mA Methylation in Regulation of Antiviral Innate Immunity.mA甲基化在抗病毒天然免疫调控中的作用
Viruses. 2024 Apr 13;16(4):601. doi: 10.3390/v16040601.
Cell Biosci. 2021 Jan 11;11(1):15. doi: 10.1186/s13578-020-00513-0.
4
Hepatitis B virus X protein recruits methyltransferases to affect cotranscriptional N6-methyladenosine modification of viral/host RNAs.乙型肝炎病毒 X 蛋白招募甲基转移酶来影响病毒/宿主 RNA 的共转录 N6-甲基腺苷修饰。
Proc Natl Acad Sci U S A. 2021 Jan 19;118(3). doi: 10.1073/pnas.2019455118.
5
Hepatitis B Virus Cure: Targets and Future Therapies.乙型肝炎病毒治愈:靶点和未来疗法。
Int J Mol Sci. 2020 Dec 28;22(1):213. doi: 10.3390/ijms22010213.
6
Epitranscriptomic(N6-methyladenosine) Modification of Viral RNA and Virus-Host Interactions.病毒RNA的表观转录组学(N6-甲基腺苷)修饰与病毒-宿主相互作用
Front Cell Infect Microbiol. 2020 Nov 24;10:584283. doi: 10.3389/fcimb.2020.584283. eCollection 2020.
7
The significance of m6A RNA methylation regulators in predicting the prognosis and clinical course of HBV-related hepatocellular carcinoma.m6A RNA 甲基化调节剂在预测 HBV 相关肝细胞癌的预后和临床病程中的意义。
Mol Med. 2020 Jun 17;26(1):60. doi: 10.1186/s10020-020-00185-z.
8
Regulation of Viral Infection by the RNA Modification -Methyladenosine.RNA 修饰——甲基腺苷对病毒感染的调控。
Annu Rev Virol. 2019 Sep 29;6(1):235-253. doi: 10.1146/annurev-virology-092818-015559. Epub 2019 Jul 5.
9
Expression profiles and prognostic significance of RNA N6-methyladenosine-related genes in patients with hepatocellular carcinoma: evidence from independent datasets.RNA N6-甲基腺苷相关基因在肝细胞癌患者中的表达谱及预后意义:来自独立数据集的证据
Cancer Manag Res. 2019 May 1;11:3921-3931. doi: 10.2147/CMAR.S191565. eCollection 2019.
10
N-Methyladenosine and Viral Infection.N-甲基腺苷与病毒感染
Front Microbiol. 2019 Mar 5;10:417. doi: 10.3389/fmicb.2019.00417. eCollection 2019.