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通过 CAGE 和天然 RNA 测序方法探索人类猴痘病毒的转录组特征。

Exploring the transcriptomic profile of human monkeypox virus via CAGE and native RNA sequencing approaches.

机构信息

Department of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.

National Laboratory of Virology, Szentágothai Research Centre, University of Pécs, Pécs, Hungary.

出版信息

mSphere. 2024 Sep 25;9(9):e0035624. doi: 10.1128/msphere.00356-24. Epub 2024 Aug 27.

DOI:10.1128/msphere.00356-24
PMID:39191390
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11423596/
Abstract

In this study, we employed short- and long-read sequencing technologies to delineate the transcriptional architecture of the human monkeypox virus and to identify key regulatory elements that govern its gene expression. Specifically, we conducted a transcriptomic analysis to annotate the transcription start sites (TSSs) and transcription end sites (TESs) of the virus by utilizing Cap Analysis of gene expression sequencing on the Illumina platform and direct RNA sequencing on the Oxford Nanopore technology device. Our investigations uncovered significant complexity in the use of alternative TSSs and TESs in viral genes. In this research, we also detected the promoter elements and poly(A) signals associated with the viral genes. Additionally, we identified novel genes in both the left and right variable regions of the viral genome.IMPORTANCEGenerally, gaining insight into how the transcription of a virus is regulated offers insights into the key mechanisms that control its life cycle. The recent outbreak of the human monkeypox virus has underscored the necessity of understanding the basic biology of its causative agent. Our results are pivotal for constructing a comprehensive transcriptomic atlas of the human monkeypox virus, providing valuable resources for future studies.

摘要

在这项研究中,我们采用短读长读测序技术来描绘人类猴痘病毒的转录结构,并鉴定出控制其基因表达的关键调节元件。具体来说,我们通过在 Illumina 平台上进行 Cap 分析基因表达测序和在 Oxford Nanopore 技术设备上进行直接 RNA 测序,进行了转录组分析以注释病毒的转录起始位点(TSS)和转录终止位点(TES)。我们的研究揭示了病毒基因中使用替代 TSS 和 TES 的显著复杂性。在这项研究中,我们还检测到与病毒基因相关的启动子元件和 poly(A)信号。此外,我们在病毒基因组的左和右可变区中鉴定出了新的基因。

重要性

一般来说,深入了解病毒的转录是如何调控的,可以深入了解控制其生命周期的关键机制。最近人类猴痘病毒的爆发突显了了解其病原体基本生物学的必要性。我们的研究结果对于构建人类猴痘病毒的综合转录组图谱至关重要,为未来的研究提供了有价值的资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4619/11423596/882e5dd9b3b8/msphere.00356-24.f008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4619/11423596/882e5dd9b3b8/msphere.00356-24.f008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4619/11423596/a3d463beaebd/msphere.00356-24.f001.jpg
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本文引用的文献

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Monkeypox virus genomic accordion strategies.猴痘病毒基因组手风琴策略。
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Molecular evolution of 2022 multi-country outbreak-causing monkeypox virus Clade IIb.2022年多国猴痘疫情致病病毒分支IIb的分子进化
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Clade I-Associated Mpox Cases Associated with Sexual Contact, the Democratic Republic of the Congo.I 型分支相关猴痘病例与性接触相关,刚果民主共和国。
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