Evidence map›Paper›PMID 26129912›Full record

ArticleBMC microbiology2015

Characterization of pseudorabies virus transcriptome by Illumina sequencing.

Péter Oláh, Dóra Tombácz, Nándor Póka, Zsolt Csabai, István Prazsák, Zsolt Boldogkői

Open access · goldAbstract read
In one paragraph

Article in BMC microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.9field-weighted citation impact, top 6% of its field
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

26 citing papers in PubMed, 39 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Péter OláhDepartment of Medical Biology, Faculty of Medicine, University of Szeged, Szeged, Hungary. olah.peter@med.u-szeged.hu.
Dóra TombáczDepartment of Medical Biology, Faculty of Medicine, University of Szeged, Szeged, Hungary. tombacz.dora@med.u-szeged.hu.
Nándor PókaDepartment of Medical Biology, Faculty of Medicine, University of Szeged, Szeged, Hungary. poka.nandor@med.u-szeged.hu.
Zsolt CsabaiDepartment of Medical Biology, Faculty of Medicine, University of Szeged, Szeged, Hungary. csabai.zsolt@med.u-szeged.hu.
István PrazsákDepartment of Medical Biology, Faculty of Medicine, University of Szeged, Szeged, Hungary. prazsak.istvan@med.u-szeged.hu.
Zsolt BoldogkőiDepartment of Medical Biology, Faculty of Medicine, University of Szeged, Szeged, Hungary. boldogkoi.zsolt@med.u-szeged.hu.
University of Szeged · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPseudorabies virus is a widely-studied model organism of the Herpesviridae family, with a compact genome arrangement of 72 known coding sequences. In order to obtain an up-to-date genetic map of the virus, a combination of RNA-sequencing approaches were applied, as recent advancements in high-throughput sequencing methods have provided a wealth of information on novel RNA species and transcript isoforms, revealing additional layers of transcriptome complexity in several viral species.

resultsThe total RNA content and polyadenylation landscape of pseudorabies virus were characterized for the first time at high coverage by Illumina high-throughput sequencing of cDNA samples collected during the lytic infectious cycle. As anticipated, nearly all of the viral genome was transcribed, with the exception of loci in the large internal and terminal repeats, and several small intergenic repetitive sequences. Our findings included a small novel polyadenylated non-coding RNA near an origin of replication, and the single-base resolution mapping of 3' UTRs across the viral genome. Alternative polyadenylation sites were found in a number of genes and a novel alternative splice site was characterized in the ep0 gene, while previously known splicing events were confirmed, yielding no alternative splice isoforms. Additionally, we detected the active polyadenylation of transcripts earlier believed to be transcribed as part of polycistronic RNAs.

conclusionTo the best of our knowledge, the present work has furnished the highest-resolution transcriptome map of an alphaherpesvirus to date, and reveals further complexities of viral gene expression, with the identification of novel transcript boundaries, alternative splicing of the key transactivator EP0, and a highly abundant, novel non-coding RNA near the lytic replication origin. These advances provide a detailed genetic map of PRV for future research.

Indexed as

Gene Expression ProfilingGenome, ViralHerpesvirus 1, SuidHigh-Throughput Nucleotide SequencingMolecular Sequence DataPolyadenylationRNA, MessengerRNA Splice SitesRNA, ViralSequence Analysis, RNARNA, MessengerRNA Splice SitesRNA, Viral

Identifiers

PMID26129912
PMCPMC4487798
OpenAlexW1571152990

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.