rRFtargetDB: a database of Ago1-mediated targets of ribosomal RNA fragments.

IF 4.2 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY RNA Pub Date : 2025-01-09 DOI:10.1261/rna.080285.124
Lingyu Guan, Sathyanarayanan Vaidhyanathan, Andrey Grigoriev
{"title":"rRFtargetDB: a database of Ago1-mediated targets of ribosomal RNA fragments.","authors":"Lingyu Guan, Sathyanarayanan Vaidhyanathan, Andrey Grigoriev","doi":"10.1261/rna.080285.124","DOIUrl":null,"url":null,"abstract":"<p><p>rRNA-derived fragments (rRFs) are a class of emerging post-transcriptional regulators of gene expression likely binding to the transcripts of target genes. However, the lack of knowledge about such targets hinders our understanding of rRF functions or binding mechanisms. The paucity of resources supporting the identification of the targets of rRFs creates a bottleneck in the fast-developing field. We have previously analyzed chimeric reads in crosslinked Argonaute1-RNA complexes to help infer the guide-target pairs and binding mechanisms of multiple rRFs based on experimental data in human HEK293 cells. To efficiently disseminate these results to the research community, we designed a web-based database rRFtargetDB that preserves most of the experimental results after removal of noise and has a user-friendly interface with flexible query options and filters allowing users to obtain comprehensive information on rRFs (or targets) of interest. rRFtargetDB is populated by ~163,000 experimentally determined unique rRF-mRNA pairs (~60,000 supported by ≥2 reads). Almost 30,000 rRF isoforms produced >385 000 (>156 000 with ≥2 reads) chimeras with all types of RNA targets (mRNAs and non-coding RNAs). Further analyses suggested hypothetical modes of interactions, supported by secondary structures of potential guide-target hybrids and binding motifs, essential for understanding the targeting mechanisms of rRFs. All these results (ranging from the weakest to the strongest experimental support) are presented in rRFtargetDB, whose goal is to provide a resource for building users' hypotheses on potential roles of rRFs. Further, we illustrate the value/application of the database on several examples. rRFtargetDB is freely accessible at https://grigoriev-lab.camden.rutgers.edu/tardb.</p>","PeriodicalId":21401,"journal":{"name":"RNA","volume":" ","pages":""},"PeriodicalIF":4.2000,"publicationDate":"2025-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"RNA","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1261/rna.080285.124","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

rRNA-derived fragments (rRFs) are a class of emerging post-transcriptional regulators of gene expression likely binding to the transcripts of target genes. However, the lack of knowledge about such targets hinders our understanding of rRF functions or binding mechanisms. The paucity of resources supporting the identification of the targets of rRFs creates a bottleneck in the fast-developing field. We have previously analyzed chimeric reads in crosslinked Argonaute1-RNA complexes to help infer the guide-target pairs and binding mechanisms of multiple rRFs based on experimental data in human HEK293 cells. To efficiently disseminate these results to the research community, we designed a web-based database rRFtargetDB that preserves most of the experimental results after removal of noise and has a user-friendly interface with flexible query options and filters allowing users to obtain comprehensive information on rRFs (or targets) of interest. rRFtargetDB is populated by ~163,000 experimentally determined unique rRF-mRNA pairs (~60,000 supported by ≥2 reads). Almost 30,000 rRF isoforms produced >385 000 (>156 000 with ≥2 reads) chimeras with all types of RNA targets (mRNAs and non-coding RNAs). Further analyses suggested hypothetical modes of interactions, supported by secondary structures of potential guide-target hybrids and binding motifs, essential for understanding the targeting mechanisms of rRFs. All these results (ranging from the weakest to the strongest experimental support) are presented in rRFtargetDB, whose goal is to provide a resource for building users' hypotheses on potential roles of rRFs. Further, we illustrate the value/application of the database on several examples. rRFtargetDB is freely accessible at https://grigoriev-lab.camden.rutgers.edu/tardb.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
rRFtargetDB: ago1介导的核糖体RNA片段靶点数据库。
rrna衍生片段(rfs)是一类新兴的转录后基因表达调控因子,可能与靶基因的转录本结合。然而,缺乏对这些靶点的了解阻碍了我们对rRF功能或结合机制的理解。支持确定区域资源基金目标的资源缺乏,在这个快速发展的领域造成了瓶颈。我们之前分析了交联Argonaute1-RNA复合物的嵌合读取,以帮助推断基于人HEK293细胞的实验数据的多种rRFs的引导靶标对和结合机制。为了有效地将这些结果传播到研究界,我们设计了一个基于web的数据库rRFtargetDB,它保留了去除噪声后的大部分实验结果,并且具有用户友好的界面,具有灵活的查询选项和过滤器,允许用户获得有关感兴趣的rrf(或目标)的全面信息。rRFtargetDB由约163,000对实验确定的独特rRF-mRNA对填充(约60,000对由≥2个reads支持)。近30,000个rRF亚型与所有类型的RNA靶标(mrna和非编码RNA)产生> 385,000(> 156,000,≥2个reads)嵌合体。进一步的分析提出了相互作用的假设模式,这些模式由潜在的导靶杂合体和结合基序的二级结构支持,这对于理解rfs的靶向机制至关重要。所有这些结果(从最弱到最强的实验支持)都在rRFtargetDB中提供,其目标是为构建用户对rrf潜在角色的假设提供资源。此外,我们通过几个例子说明了数据库的价值/应用。rRFtargetDB可在https://grigoriev-lab.camden.rutgers.edu/tardb免费访问。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
RNA
RNA 生物-生化与分子生物学
CiteScore
8.30
自引率
2.20%
发文量
101
审稿时长
2.6 months
期刊介绍: RNA is a monthly journal which provides rapid publication of significant original research in all areas of RNA structure and function in eukaryotic, prokaryotic, and viral systems. It covers a broad range of subjects in RNA research, including: structural analysis by biochemical or biophysical means; mRNA structure, function and biogenesis; alternative processing: cis-acting elements and trans-acting factors; ribosome structure and function; translational control; RNA catalysis; tRNA structure, function, biogenesis and identity; RNA editing; rRNA structure, function and biogenesis; RNA transport and localization; regulatory RNAs; large and small RNP structure, function and biogenesis; viral RNA metabolism; RNA stability and turnover; in vitro evolution; and RNA chemistry.
期刊最新文献
Exploring the therapeutic potential of modulating nonsense-mediated mRNA decay. A general and biomedical perspective of viral quasispecies. RNA-binding proteins in disease etiology: fragile X syndrome and spinal muscular atrophy. Mitochondrial tRNA modifications: functions, diseases caused by their loss, and treatment strategies. N 6-methyladenosine reader YTHDF2 in cell state transition and antitumor immunity.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1