Characterization of Novel Transcripts in Pseudorabies Virus

In this study we identified two 3′-coterminal RNA molecules in the pseudorabies virus. The highly abundant short transcript (CTO-S) proved to be encoded between the ul21 and ul22 genes in close vicinity of the replication origin (OriL) of the virus. The less abundant long RNA molecule (CTO-L) is a t...

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Main Authors: Dóra Tombácz, Zsolt Csabai, Péter Oláh, Zoltán Havelda, Donald Sharon, Michael Snyder, Zsolt Boldogkői
Format: Article
Language:English
Published: MDPI AG 2015-05-01
Series:Viruses
Subjects:
Online Access:http://www.mdpi.com/1999-4915/7/5/2727
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spelling doaj-b02051b9f1a84ceb8a2d03e79accc2d62020-11-24T22:52:36ZengMDPI AGViruses1999-49152015-05-01752727274410.3390/v7052727v7052727Characterization of Novel Transcripts in Pseudorabies VirusDóra Tombácz0Zsolt Csabai1Péter Oláh2Zoltán Havelda3Donald Sharon4Michael Snyder5Zsolt Boldogkői6Department of Medical Biology, Faculty of Medicine, University of Szeged, Somogyi B. u. 4., Szeged H-6720, HungaryDepartment of Medical Biology, Faculty of Medicine, University of Szeged, Somogyi B. u. 4., Szeged H-6720, HungaryDepartment of Medical Biology, Faculty of Medicine, University of Szeged, Somogyi B. u. 4., Szeged H-6720, HungaryAgricultural Biotechnology Center, Institute for Plant Biotechnology, Plant Developmental Biology Group, Szent-Györgyi A. u. 4, Gödöllő H-2100, HungaryDepartment of Genetics, School of Medicine, Stanford University, 300 Pasteur Dr., Stanford, CA 94305-5120, USADepartment of Genetics, School of Medicine, Stanford University, 300 Pasteur Dr., Stanford, CA 94305-5120, USADepartment of Medical Biology, Faculty of Medicine, University of Szeged, Somogyi B. u. 4., Szeged H-6720, HungaryIn this study we identified two 3′-coterminal RNA molecules in the pseudorabies virus. The highly abundant short transcript (CTO-S) proved to be encoded between the ul21 and ul22 genes in close vicinity of the replication origin (OriL) of the virus. The less abundant long RNA molecule (CTO-L) is a transcriptional readthrough product of the ul21 gene and overlaps OriL. These polyadenylated RNAs were characterized by ascertaining their nucleotide sequences with the Illumina HiScanSQ and Pacific Biosciences Real-Time (PacBio RSII) sequencing platforms and by analyzing their transcription kinetics through use of multi-time-point Real-Time RT-PCR and the PacBio RSII system. It emerged that transcription of the CTOs is fully dependent on the viral transactivator protein IE180 and CTO-S is not a microRNA precursor. We propose an interaction between the transcription and replication machineries at this genomic location, which might play an important role in the regulation of DNA synthesis.http://www.mdpi.com/1999-4915/7/5/2727non-coding RNApseudorabies virusherpesvirusRNA sequencingDNA replication
collection DOAJ
language English
format Article
sources DOAJ
author Dóra Tombácz
Zsolt Csabai
Péter Oláh
Zoltán Havelda
Donald Sharon
Michael Snyder
Zsolt Boldogkői
spellingShingle Dóra Tombácz
Zsolt Csabai
Péter Oláh
Zoltán Havelda
Donald Sharon
Michael Snyder
Zsolt Boldogkői
Characterization of Novel Transcripts in Pseudorabies Virus
Viruses
non-coding RNA
pseudorabies virus
herpesvirus
RNA sequencing
DNA replication
author_facet Dóra Tombácz
Zsolt Csabai
Péter Oláh
Zoltán Havelda
Donald Sharon
Michael Snyder
Zsolt Boldogkői
author_sort Dóra Tombácz
title Characterization of Novel Transcripts in Pseudorabies Virus
title_short Characterization of Novel Transcripts in Pseudorabies Virus
title_full Characterization of Novel Transcripts in Pseudorabies Virus
title_fullStr Characterization of Novel Transcripts in Pseudorabies Virus
title_full_unstemmed Characterization of Novel Transcripts in Pseudorabies Virus
title_sort characterization of novel transcripts in pseudorabies virus
publisher MDPI AG
series Viruses
issn 1999-4915
publishDate 2015-05-01
description In this study we identified two 3′-coterminal RNA molecules in the pseudorabies virus. The highly abundant short transcript (CTO-S) proved to be encoded between the ul21 and ul22 genes in close vicinity of the replication origin (OriL) of the virus. The less abundant long RNA molecule (CTO-L) is a transcriptional readthrough product of the ul21 gene and overlaps OriL. These polyadenylated RNAs were characterized by ascertaining their nucleotide sequences with the Illumina HiScanSQ and Pacific Biosciences Real-Time (PacBio RSII) sequencing platforms and by analyzing their transcription kinetics through use of multi-time-point Real-Time RT-PCR and the PacBio RSII system. It emerged that transcription of the CTOs is fully dependent on the viral transactivator protein IE180 and CTO-S is not a microRNA precursor. We propose an interaction between the transcription and replication machineries at this genomic location, which might play an important role in the regulation of DNA synthesis.
topic non-coding RNA
pseudorabies virus
herpesvirus
RNA sequencing
DNA replication
url http://www.mdpi.com/1999-4915/7/5/2727
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