Long-read Transcriptomics of Caviid Gammaherpesvirus 1: Compiling a Comprehensive RNA Atlas.

Gábor Torma, Ákos Dörmő, Ádám Fülöp, Dóra Tombácz, Máté Mizik, Amanda M Pretory, See-Chi Lee, Zsolt Toth, Zsolt Boldogkői
{"title":"Long-read Transcriptomics of Caviid Gammaherpesvirus 1: Compiling a Comprehensive RNA Atlas.","authors":"Gábor Torma, Ákos Dörmő, Ádám Fülöp, Dóra Tombácz, Máté Mizik, Amanda M Pretory, See-Chi Lee, Zsolt Toth, Zsolt Boldogkői","doi":"10.1101/2024.12.11.627975","DOIUrl":null,"url":null,"abstract":"<p><p>Caviid gammaherpesvirus 1 (CaGHV-1), formerly known as the guinea pig herpes-like virus, is an oncogenic gammaherpesvirus with a sequenced genome but an as-yet uncharacterized transcriptome. Using nanopore long-read RNA sequencing, we annotated the CaGHV-1 genome and constructed a detailed transcriptomic atlas. Our findings reveal diverse viral mRNAs and non-coding RNAs, along with mapped promoter elements for each viral gene. We demonstrated that the CaGHV-1 RTA lytic cycle transcription factor activates its own promoter, similar to KSHV, and that the CaGHV-1 ORF50 promoter responds to RTA proteins from other gammaherpesviruses, highlighting the evolutionary conservation of RTA-mediated transcriptional mechanisms. Additionally, our analysis uncovered extensive transcriptional overlap within the viral genome, suggesting a role in regulating global gene expression. Given its tumorigenic properties, broad host range, and non-human pathogenicity, this work establishes CaGHV-1 as a promising small animal model for investigating human gammaherpesvirus pathogenesis.</p>","PeriodicalId":519960,"journal":{"name":"bioRxiv : the preprint server for biology","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11661164/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"bioRxiv : the preprint server for biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.12.11.627975","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Caviid gammaherpesvirus 1 (CaGHV-1), formerly known as the guinea pig herpes-like virus, is an oncogenic gammaherpesvirus with a sequenced genome but an as-yet uncharacterized transcriptome. Using nanopore long-read RNA sequencing, we annotated the CaGHV-1 genome and constructed a detailed transcriptomic atlas. Our findings reveal diverse viral mRNAs and non-coding RNAs, along with mapped promoter elements for each viral gene. We demonstrated that the CaGHV-1 RTA lytic cycle transcription factor activates its own promoter, similar to KSHV, and that the CaGHV-1 ORF50 promoter responds to RTA proteins from other gammaherpesviruses, highlighting the evolutionary conservation of RTA-mediated transcriptional mechanisms. Additionally, our analysis uncovered extensive transcriptional overlap within the viral genome, suggesting a role in regulating global gene expression. Given its tumorigenic properties, broad host range, and non-human pathogenicity, this work establishes CaGHV-1 as a promising small animal model for investigating human gammaherpesvirus pathogenesis.

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
海腔γ疱疹病毒1的长读转录组学:编制一个全面的RNA图谱。
Caviid γ疱疹病毒1 (CaGHV-1),以前被称为豚鼠疱疹样病毒,是一种致癌的γ疱疹病毒,基因组已测序,但转录组尚未表征。利用纳米孔长读RNA测序,我们对CaGHV-1基因组进行了注释,并构建了详细的转录组图谱。我们的发现揭示了不同的病毒mrna和非编码rna,以及每个病毒基因的映射启动子元件。我们证明了CaGHV-1 RTA裂解周期转录因子激活其自身的启动子,类似于KSHV,并且CaGHV-1 ORF50启动子响应来自其他γ疱疹病毒的RTA蛋白,突出了RTA介导的转录机制的进化保守性。此外,我们的分析揭示了病毒基因组中广泛的转录重叠,表明其在调节全球基因表达方面发挥作用。鉴于其致瘤性、广泛的宿主范围和非人类致病性,本研究建立了CaGHV-1作为研究人类伽玛疱疹病毒发病机制的有希望的小动物模型。重要性:伽玛疱疹病毒发病机制的分子基础仍然知之甚少,部分原因是动物模型有限。这项研究提供了第一个综合的CaGHV-1转录组图谱,突出了编码和非编码rna,并揭示了驱动病毒基因表达的调控元件。对CaGHV-1 RTA转录因子的功能研究表明,它能够自激活和交叉激活同源γ疱疹病毒的启动子,反映了转录控制的保守机制。这些发现巩固了CaGHV-1作为一种独特和通用的小动物模型,为在受控实验系统中研究γ疱疹病毒复制、转录调控和肿瘤发生提供了新的机会。
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
自引率
0.00%
发文量
0
期刊最新文献
Identifying unmeasured heterogeneity in microbiome data via quantile thresholding (QuanT). Detection of Iron Protein Supercomplexes in Pseudomonas aeruginosa by Native Metalloproteomics. Quantifying the impact of antibiotic use and genetic determinants of resistance on bacterial lineage dynamics. Deciphering population-level response under spatial drug heterogeneity on microhabitat structures. Beta cell dysfunction occurs independently of insulitis in type 1 diabetes pathogenesis.
×
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