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
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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.

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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。
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