• 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

使RNA修饰对蛋白质相互作用的影响合理化。

Rationalizing the effects of RNA modifications on protein interactions.

作者信息

Vandelli Andrea, Broglia Laura, Armaos Alexandros, Delli Ponti Riccardo, Tartaglia Gian Gaetano

机构信息

Centre for Human Technologies (CHT), RNA System Biology Lab, Istituto Italiano di Tecnologia (IIT), Via Enrico Melen, 83, 16152 Genova, Italy.

出版信息

Mol Ther Nucleic Acids. 2024 Nov 15;35(4):102391. doi: 10.1016/j.omtn.2024.102391. eCollection 2024 Dec 10.

DOI:10.1016/j.omtn.2024.102391
PMID:39717617
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11664407/
Abstract

RNA modifications play a crucial role in regulating gene expression by altering RNA structure and modulating interactions with RNA-binding proteins (RBPs). In this study, we explore the impact of specific RNA chemical modifications-N-methyladenosine (m⁶A), A-to-I editing, and pseudouridine (Ψ)-on RNA secondary structure and protein-RNA interactions. Utilizing genome-wide data, including RNA secondary structure predictions and protein-RNA interaction datasets, we classify proteins into distinct categories based on their binding behaviors: modification specific and structure independent, or modification unspecific and structure dependent. For instance, m⁶A readers such as YTHDF2 exhibit modification-specific and structure-independent binding, consistently recognizing m⁶A regardless of structural changes. Conversely, proteins such as U2AF2 display modification-unspecific and structure-dependent behavior, altering their binding preferences in response to structural changes induced by different modifications. A-to-I editing, which causes significant structural changes, typically reduces protein interactions, while Ψ enhances RNA structural stability, albeit with variable effects on protein binding. To predict these interactions, we developed the RAPID 2.2 algorithm, which computes the effects of RNA modifications on protein-RNA binding propensities. This algorithm enables the prediction and analysis of RNA modifications' impact on protein interactions, offering new insights into RNA biology and engineering.

摘要

RNA修饰通过改变RNA结构和调节与RNA结合蛋白(RBP)的相互作用,在基因表达调控中发挥关键作用。在本研究中,我们探讨了特定RNA化学修饰——N⁶-甲基腺苷(m⁶A)、A到I编辑和假尿苷(Ψ)——对RNA二级结构和蛋白质-RNA相互作用的影响。利用全基因组数据,包括RNA二级结构预测和蛋白质-RNA相互作用数据集,我们根据蛋白质的结合行为将其分为不同类别:修饰特异性和结构非依赖性,或修饰非特异性和结构依赖性。例如,YTHDF2等m⁶A阅读蛋白表现出修饰特异性和结构非依赖性结合,无论结构变化如何,都能持续识别m⁶A。相反,U2AF2等蛋白质表现出修饰非特异性和结构依赖性行为,会根据不同修饰诱导的结构变化改变其结合偏好。A到I编辑会导致显著的结构变化,通常会减少蛋白质相互作用,而Ψ则增强RNA结构稳定性,尽管对蛋白质结合的影响各不相同。为了预测这些相互作用,我们开发了RAPID 2.2算法,该算法计算RNA修饰对蛋白质-RNA结合倾向的影响。该算法能够预测和分析RNA修饰对蛋白质相互作用的影响,为RNA生物学和工程学提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ba/11664407/f50fb2cdb221/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ba/11664407/1aa607a3ee8d/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ba/11664407/c143c36de729/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ba/11664407/1a669612fba8/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ba/11664407/c2d8d3375e1d/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ba/11664407/9e9171976995/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ba/11664407/7fa7f392a355/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ba/11664407/f50fb2cdb221/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ba/11664407/1aa607a3ee8d/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ba/11664407/c143c36de729/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ba/11664407/1a669612fba8/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ba/11664407/c2d8d3375e1d/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ba/11664407/9e9171976995/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ba/11664407/7fa7f392a355/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ba/11664407/f50fb2cdb221/gr6.jpg

相似文献

1
Rationalizing the effects of RNA modifications on protein interactions.使RNA修饰对蛋白质相互作用的影响合理化。
Mol Ther Nucleic Acids. 2024 Nov 15;35(4):102391. doi: 10.1016/j.omtn.2024.102391. eCollection 2024 Dec 10.
2
Beyond reader proteins: RNA binding proteins and RNA modifications in conversation to regulate gene expression.超越读者蛋白:RNA 结合蛋白和 RNA 修饰物的对话调控基因表达。
Wiley Interdiscip Rev RNA. 2024 Mar-Apr;15(2):e1834. doi: 10.1002/wrna.1834.
3
Pseudouridine and -methyladenosine modifications weaken PUF protein/RNA interactions.假尿苷和N6-甲基腺苷修饰会削弱PUF蛋白与RNA的相互作用。
RNA. 2017 May;23(5):611-618. doi: 10.1261/rna.060053.116. Epub 2017 Jan 30.
4
Random Forest model reveals the interaction between N6-methyladenosine modifications and RNA-binding proteins.随机森林模型揭示了N6-甲基腺嘌呤修饰与RNA结合蛋白之间的相互作用。
iScience. 2023 Feb 20;26(3):106250. doi: 10.1016/j.isci.2023.106250. eCollection 2023 Mar 17.
5
Writers, readers, and erasers RNA modifications and drug resistance in cancer.RNA 修饰与癌症的药物耐药性:作者、读者和橡皮擦
Mol Cancer. 2024 Aug 30;23(1):178. doi: 10.1186/s12943-024-02089-6.
6
A high-throughput approach to predict A-to-I effects on RNA structure indicates a change of double-stranded content in noncoding RNAs.一种高通量方法预测 A-to-I 对 RNA 结构的影响,表明非编码 RNA 中双链含量的变化。
IUBMB Life. 2023 May;75(5):411-426. doi: 10.1002/iub.2673. Epub 2022 Sep 24.
7
mito-Ψ-Seq: A High-Throughput Method for Systematic Mapping of Pseudouridine Within Mitochondrial RNA.mito-Ψ-Seq:一种系统绘制线粒体 RNA 内假尿嘧啶的高通量方法。
Methods Mol Biol. 2021;2192:103-115. doi: 10.1007/978-1-0716-0834-0_9.
8
RNA modifications in female reproductive physiology and disease: emerging roles and clinical implications.RNA修饰在女性生殖生理与疾病中的作用:新出现的作用及临床意义
Hum Reprod Update. 2025 Mar 27. doi: 10.1093/humupd/dmaf005.
9
Global RNA modifications to the MALAT1 triple helix differentially affect thermostability and weaken binding to METTL16.全球 RNA 修饰对 MALAT1 三螺旋的影响不同,会影响热稳定性并削弱与 METTL16 的结合。
J Biol Chem. 2024 Jan;300(1):105548. doi: 10.1016/j.jbc.2023.105548. Epub 2023 Dec 11.
10
RMBase v2.0: deciphering the map of RNA modifications from epitranscriptome sequencing data.RMBase v2.0:从转录组测序数据中破译 RNA 修饰的图谱。
Nucleic Acids Res. 2018 Jan 4;46(D1):D327-D334. doi: 10.1093/nar/gkx934.

引用本文的文献

1
catGRANULE 2.0: accurate predictions of liquid-liquid phase separating proteins at single amino acid resolution.catGRANULE 2.0:在单氨基酸分辨率下对液-液相分离蛋白进行准确预测。
Genome Biol. 2025 Feb 20;26(1):33. doi: 10.1186/s13059-025-03497-7.

本文引用的文献

1
Subgenomic flaviviral RNAs and human proteins: exploration of anti-host defense mechanisms.亚基因组黄病毒RNA与人类蛋白质:抗宿主防御机制的探索
Comput Struct Biotechnol J. 2024 Sep 30;23:3527-3536. doi: 10.1016/j.csbj.2024.09.029. eCollection 2024 Dec.
2
2'-O-methylation at internal sites on mRNA promotes mRNA stability.mRNA 内部位点的 2'-O-甲基化促进 mRNA 的稳定性。
Mol Cell. 2024 Jun 20;84(12):2320-2336.e6. doi: 10.1016/j.molcel.2024.04.011.
3
Pseudouridine and 1-methylpseudouridine as potent nucleotide analogues for RNA therapy and vaccine development.
假尿苷和1-甲基假尿苷作为RNA治疗和疫苗开发的有效核苷酸类似物。
RSC Chem Biol. 2024 Mar 19;5(5):418-425. doi: 10.1039/d4cb00022f. eCollection 2024 May 8.
4
RNA: The Unsuspected Conductor in the Orchestra of Macromolecular Crowding.RNA:大分子拥挤环境中的幕后指挥者
Chem Rev. 2024 Apr 24;124(8):4734-4777. doi: 10.1021/acs.chemrev.3c00575. Epub 2024 Apr 5.
5
Adenine Methylation Enhances the Conformational Flexibility of an RNA Hairpin Tetraloop.腺嘌呤甲基化增强 RNA 发夹四环的构象灵活性。
J Phys Chem B. 2024 Apr 4;128(13):3157-3166. doi: 10.1021/acs.jpcb.4c00522. Epub 2024 Mar 27.
6
Beyond reader proteins: RNA binding proteins and RNA modifications in conversation to regulate gene expression.超越读者蛋白:RNA 结合蛋白和 RNA 修饰物的对话调控基因表达。
Wiley Interdiscip Rev RNA. 2024 Mar-Apr;15(2):e1834. doi: 10.1002/wrna.1834.
7
Prediction of protein-RNA interactions from single-cell transcriptomic data.从单细胞转录组数据中预测蛋白质-RNA 相互作用。
Nucleic Acids Res. 2024 Apr 12;52(6):e31. doi: 10.1093/nar/gkae076.
8
Unveiling the role of PUS7-mediated pseudouridylation in host protein interactions specific for the SARS-CoV-2 RNA genome.揭示PUS7介导的假尿苷化在针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)RNA基因组的宿主蛋白相互作用中的作用。
Mol Ther Nucleic Acids. 2023 Oct 25;34:102052. doi: 10.1016/j.omtn.2023.102052. eCollection 2023 Dec 12.
9
Modified RNAs and predictions with the ViennaRNA Package.修饰 RNA 及其与 ViennaRNA 包的预测。
Bioinformatics. 2023 Nov 1;39(11). doi: 10.1093/bioinformatics/btad696.
10
Interconnections between mA RNA modification, RNA structure, and protein-RNA complex assembly.mRNA 修饰、RNA 结构和蛋白-RNA 复合物组装之间的相互联系。
Life Sci Alliance. 2023 Nov 7;7(1). doi: 10.26508/lsa.202302240. Print 2024 Jan.