Evidence map›Paper›PMID 39191390›Full record

ArticlemSphere2024

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

Gergely Ármin Nagy, Dóra Tombácz, István Prazsák, Zsolt Csabai, Ákos Dörmő, Gábor Gulyás, Gábor Kemenesi, Gábor E Tóth, Jiří Holoubek, Daniel Růžek and 2 more

Abstract read
In one paragraph

Article in mSphere, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Gergely Ármin Nagy *Department of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Dóra Tombácz *Department of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.ORCID 0000-0001-5520-2978
István PrazsákDepartment of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Zsolt CsabaiDepartment of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Ákos DörmőDepartment of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Gábor GulyásDepartment of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Gábor KemenesiNational Laboratory of Virology, Szentágothai Research Centre, University of Pécs, Pécs, Hungary.
Gábor E TóthNational Laboratory of Virology, Szentágothai Research Centre, University of Pécs, Pécs, Hungary.
Jiří HoloubekVeterinary Research Institute, Brno, Czechia.
Daniel RůžekVeterinary Research Institute, Brno, Czechia.
Balázs KakukDepartment of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Zsolt BoldogkőiDepartment of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.ORCID 0000-0003-1184-7293

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Sequence Analysis, RNATranscription Initiation SiteTranscriptomeGene Expression ProfilingGenome, ViralHigh-Throughput Nucleotide SequencingHumansMonkeypox virusPromoter Regions, GeneticRNA, ViralRNA, ViralCAGE-Seqlong-read sequencingmonkeypox virusnanopore sequencingpoxvirustranscriptome

Identifiers

PMID39191390
PMCPMC11423596

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.