• 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

LNCediting:一个lncRNA中RNA编辑功能效应的数据库。

LNCediting: a database for functional effects of RNA editing in lncRNAs.

作者信息

Gong Jing, Liu Chunjie, Liu Wei, Xiang Yu, Diao Lixia, Guo An-Yuan, Han Leng

机构信息

Department of Bioinformatics and Systems Biology, Hubei Bioinformatics & Molecular Imaging Key Laboratory, Key Laboratory of Molecular Biophysics of the Ministry of Education, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, Hubei 430074, PR China.

Department of Biochemistry and Molecular Biology, The University of Texas Health Science Center at Houston McGovern Medical School, Houston, TX 77030, USA.

出版信息

Nucleic Acids Res. 2017 Jan 4;45(D1):D79-D84. doi: 10.1093/nar/gkw835. Epub 2016 Sep 19.

DOI:10.1093/nar/gkw835
PMID:27651464
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5210611/
Abstract

RNA editing is a widespread post-transcriptional mechanism that can make a single base change on specific nucleotide sequence in an RNA transcript. RNA editing events can result in missense codon changes and modulation of alternative splicing in mRNA, and modification of regulatory RNAs and their binding sites in noncoding RNAs. Recent computational studies accurately detected more than 2 million A-to-I RNA editing sites from next-generation sequencing (NGS). However, the vast majority of these RNA editing sites have unknown functions and are in noncoding regions of the genome. To provide a useful resource for the functional effects of RNA editing in long noncoding RNAs (lncRNAs), we systematically analyzed the A-to-I editing sites in lncRNAs across human, rhesus, mouse, and fly, and observed an appreciable number of RNA editing sites which can significantly impact the secondary structures of lncRNAs and lncRNA-miRNA interactions. All the data were compiled into LNCediting, a user-friendly database (http://bioinfo.life.hust.edu.cn/LNCediting/). LNCediting provides customized tools to predict functional effects of novel editing sites in lncRNAs. We hope that it will become an important resource for exploring functions of RNA editing sites in lncRNAs.

摘要

RNA编辑是一种广泛存在的转录后机制,它可以使RNA转录本中的特定核苷酸序列发生单个碱基变化。RNA编辑事件可导致错义密码子改变以及mRNA中可变剪接的调控,还可导致非编码RNA及其结合位点的修饰。最近的计算研究从下一代测序(NGS)中准确检测到了超过200万个A-to-I RNA编辑位点。然而,这些RNA编辑位点中的绝大多数功能未知,且位于基因组的非编码区域。为了为长链非编码RNA(lncRNA)中RNA编辑的功能效应提供有用资源,我们系统分析了人类、恒河猴、小鼠和果蝇lncRNA中的A-to-I编辑位点,并观察到相当数量的RNA编辑位点会显著影响lncRNA的二级结构以及lncRNA与miRNA的相互作用。所有数据都被整合到LNCediting中,这是一个用户友好型数据库(http://bioinfo.life.hust.edu.cn/LNCediting/)。LNCediting提供了定制工具来预测lncRNA中新型编辑位点的功能效应。我们希望它将成为探索lncRNA中RNA编辑位点功能的重要资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8568/5210611/67b99effaf88/gkw835fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8568/5210611/67b99effaf88/gkw835fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8568/5210611/67b99effaf88/gkw835fig1.jpg

相似文献

1
LNCediting: a database for functional effects of RNA editing in lncRNAs.LNCediting:一个lncRNA中RNA编辑功能效应的数据库。
Nucleic Acids Res. 2017 Jan 4;45(D1):D79-D84. doi: 10.1093/nar/gkw835. Epub 2016 Sep 19.
2
lncRNASNP: a database of SNPs in lncRNAs and their potential functions in human and mouse.lncRNASNP:一个关于长链非编码RNA中的单核苷酸多态性及其在人和小鼠中潜在功能的数据库。
Nucleic Acids Res. 2015 Jan;43(Database issue):D181-6. doi: 10.1093/nar/gku1000. Epub 2014 Oct 20.
3
Noncoding regions of C. elegans mRNA undergo selective adenosine to inosine deamination and contain a small number of editing sites per transcript.秀丽隐杆线虫信使核糖核酸的非编码区域会发生选择性腺苷到次黄苷的脱氨基作用,并且每个转录本含有少量的编辑位点。
RNA Biol. 2015;12(2):162-74. doi: 10.1080/15476286.2015.1017220.
4
lncRNASNP2: an updated database of functional SNPs and mutations in human and mouse lncRNAs.lncRNASNP2:人源和鼠源长非编码 RNA 中功能 SNP 和突变的更新数据库。
Nucleic Acids Res. 2018 Jan 4;46(D1):D276-D280. doi: 10.1093/nar/gkx1004.
5
lncRNAtor: a comprehensive resource for functional investigation of long non-coding RNAs.lncRNAtor:长链非编码RNA功能研究的综合资源。
Bioinformatics. 2014 Sep 1;30(17):2480-5. doi: 10.1093/bioinformatics/btu325. Epub 2014 May 9.
6
RADAR: a rigorously annotated database of A-to-I RNA editing.RADAR:一个经过严格注释的 A 到 I RNA 编辑数据库。
Nucleic Acids Res. 2014 Jan;42(Database issue):D109-13. doi: 10.1093/nar/gkt996. Epub 2013 Oct 25.
7
LincSNP 3.0: an updated database for linking functional variants to human long non-coding RNAs, circular RNAs and their regulatory elements.LincSNP 3.0:一个更新的数据库,用于将功能变体与人类长非编码 RNA、环状 RNA 及其调控元件联系起来。
Nucleic Acids Res. 2021 Jan 8;49(D1):D1244-D1250. doi: 10.1093/nar/gkaa1037.
8
Proteogenomics of Adenosine-to-Inosine RNA Editing in the Fruit Fly.腺苷到肌苷 RNA 编辑的蛋白质基因组学在果蝇中。
J Proteome Res. 2018 Nov 2;17(11):3889-3903. doi: 10.1021/acs.jproteome.8b00553. Epub 2018 Oct 17.
9
LncRBase V.2: an updated resource for multispecies lncRNAs and ClinicLSNP hosting genetic variants in lncRNAs for cancer patients.LncRBase V.2:一个更新的多物种 lncRNA 资源,以及为癌症患者的 lncRNA 提供基因变异的 ClinicLSNP 宿主。
RNA Biol. 2021 Aug;18(8):1136-1151. doi: 10.1080/15476286.2020.1833529. Epub 2020 Oct 28.
10
COME: a robust coding potential calculation tool for lncRNA identification and characterization based on multiple features.COME:一种基于多种特征的用于lncRNA鉴定和表征的强大编码潜力计算工具。
Nucleic Acids Res. 2017 Jan 9;45(1):e2. doi: 10.1093/nar/gkw798. Epub 2016 Sep 7.

引用本文的文献

1
A-to-I edited SNHG3 promotes non-small cell lung cancer metastasis by promoting fatty acid oxidation and resisting ferroptosis.A到I编辑的SNHG3通过促进脂肪酸氧化和抵抗铁死亡来促进非小细胞肺癌转移。
Commun Biol. 2025 Sep 2;8(1):1333. doi: 10.1038/s42003-025-08776-4.
2
Advances in Detection Methods for A-to-I RNA Editing.A-to-I RNA编辑检测方法的进展
Wiley Interdiscip Rev RNA. 2025 Mar-Apr;16(2):e70014. doi: 10.1002/wrna.70014.
3
Advances in A-to-I RNA editing in cancer.癌症中A到I RNA编辑的进展。

本文引用的文献

1
RNA editing in cancer: Mechanistic, prognostic, and therapeutic implications.癌症中的RNA编辑:机制、预后及治疗意义
Mol Cell Oncol. 2015 Dec 14;3(2):e1117702. doi: 10.1080/23723556.2015.1117702. eCollection 2016 Mar.
2
Improving GENCODE reference gene annotation using a high-stringency proteogenomics workflow.利用高严格性的蛋白质基因组学工作流程改进 GENCODE 参考基因注释。
Nat Commun. 2016 Jun 2;7:11778. doi: 10.1038/ncomms11778.
3
A comprehensive overview of lncRNA annotation resources.lncRNA 注释资源的全面概述。
Mol Cancer. 2024 Dec 27;23(1):280. doi: 10.1186/s12943-024-02194-6.
4
ncRNA Editing: Functional Characterization and Computational Resources.非编码RNA编辑:功能表征与计算资源
Methods Mol Biol. 2025;2883:455-495. doi: 10.1007/978-1-0716-4290-0_20.
5
Inhibiting lncRNA NEAT1 Increases Glioblastoma Response to TMZ by Reducing Connexin 43 Expression.抑制长链非编码 RNA NEAT1 通过降低连接蛋白 43 的表达增加胶质母细胞瘤对 TMZ 的反应。
Cancer Rep (Hoboken). 2024 Oct;7(10):e70031. doi: 10.1002/cnr2.70031.
6
NERD-seq: a novel approach of Nanopore direct RNA sequencing that expands representation of non-coding RNAs.NERD-seq:一种新型的纳米孔直接 RNA 测序方法,可扩展非编码 RNA 的代表性。
Genome Biol. 2024 Aug 28;25(1):233. doi: 10.1186/s13059-024-03375-8.
7
Decoding the connection between lncRNA and obesity: Perspective from humans and .解读长链非编码RNA与肥胖之间的联系:来自人类的视角以及…… (原文此处不完整)
Heliyon. 2024 Jul 28;10(15):e35327. doi: 10.1016/j.heliyon.2024.e35327. eCollection 2024 Aug 15.
8
A-to-I edited miR-154-p13-5p inhibited cell proliferation and migration and induced apoptosis by targeting LIX1L in the bladder cancer.A到I编辑的miR-154-p13-5p通过靶向膀胱癌中的LIX1L抑制细胞增殖和迁移并诱导细胞凋亡。
J Cancer. 2024 May 13;15(12):3708-3723. doi: 10.7150/jca.93388. eCollection 2024.
9
RNA editing in host lncRNAs as potential modulator in SARS-CoV-2 variants-host immune response dynamics.宿主长链非编码RNA中的RNA编辑作为严重急性呼吸综合征冠状病毒2(SARS-CoV-2)变体-宿主免疫反应动态的潜在调节因子
iScience. 2024 Apr 29;27(6):109846. doi: 10.1016/j.isci.2024.109846. eCollection 2024 Jun 21.
10
Non-coding RNAs as therapeutic targets and biomarkers in ischaemic heart disease.非编码RNA作为缺血性心脏病的治疗靶点和生物标志物
Nat Rev Cardiol. 2024 Aug;21(8):556-573. doi: 10.1038/s41569-024-01001-5. Epub 2024 Mar 18.
Brief Bioinform. 2017 Mar 1;18(2):236-249. doi: 10.1093/bib/bbw015.
4
MiRNA-192 [corrected] and miRNA-204 Directly Suppress lncRNA HOTTIP and Interrupt GLS1-Mediated Glutaminolysis in Hepatocellular Carcinoma.微小RNA-192[校正后]和微小RNA-204直接抑制长链非编码RNA HOTTIP并中断肝细胞癌中GLS1介导的谷氨酰胺分解代谢。
PLoS Genet. 2015 Dec 28;11(12):e1005726. doi: 10.1371/journal.pgen.1005726. eCollection 2015 Dec.
5
The UCSC Genome Browser database: 2016 update.加州大学圣克鲁兹分校基因组浏览器数据库:2016年更新
Nucleic Acids Res. 2016 Jan 4;44(D1):D717-25. doi: 10.1093/nar/gkv1275. Epub 2015 Nov 20.
6
NONCODE 2016: an informative and valuable data source of long non-coding RNAs.NONCODE 2016:一个关于长链非编码RNA的信息丰富且有价值的数据源。
Nucleic Acids Res. 2016 Jan 4;44(D1):D203-8. doi: 10.1093/nar/gkv1252. Epub 2015 Nov 19.
7
SomamiR 2.0: a database of cancer somatic mutations altering microRNA-ceRNA interactions.SomamiR 2.0:一个改变微小RNA-竞争性内源RNA相互作用的癌症体细胞突变数据库。
Nucleic Acids Res. 2016 Jan 4;44(D1):D1005-10. doi: 10.1093/nar/gkv1220. Epub 2015 Nov 17.
8
Genome-wide identification and characterization of tissue-specific RNA editing events in D. melanogaster and their potential role in regulating alternative splicing.黑腹果蝇中组织特异性RNA编辑事件的全基因组鉴定与表征及其在调控可变剪接中的潜在作用。
RNA Biol. 2015;12(12):1391-401. doi: 10.1080/15476286.2015.1107703.
9
Cancer genomics: The relevance of extensive editing in tumour transcriptomes.癌症基因组学:肿瘤转录组中广泛编辑的相关性。
Nat Rev Cancer. 2015 Dec;15(12):698. doi: 10.1038/nrc4044. Epub 2015 Oct 29.
10
The Genomic Landscape and Clinical Relevance of A-to-I RNA Editing in Human Cancers.人类癌症中 A 到 I RNA 编辑的基因组景观和临床相关性。
Cancer Cell. 2015 Oct 12;28(4):515-528. doi: 10.1016/j.ccell.2015.08.013. Epub 2015 Oct 1.