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多平台分析揭示了圆环病毒复杂的转录组结构。

Multi-platform analysis reveals a complex transcriptome architecture of a circovirus.

作者信息

Moldován Norbert, Balázs Zsolt, Tombácz Dóra, Csabai Zsolt, Szűcs Attila, Snyder Michael, Boldogkői Zsolt

机构信息

Department of Medical Biology, Faculty of Medicine, University of Szeged, Szeged, Hungary.

Department of Medical Biology, Faculty of Medicine, University of Szeged, Szeged, Hungary; Department of Genetics, School of Medicine, Stanford University, Stanford, CA, USA.

出版信息

Virus Res. 2017 Jun 2;237:37-46. doi: 10.1016/j.virusres.2017.05.010. Epub 2017 May 24.

DOI:10.1016/j.virusres.2017.05.010
PMID:28549855
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5927800/
Abstract

In this study, we used Pacific Biosciences RS II long-read and Illumina HiScanSQ short-read sequencing technologies for the characterization of porcine circovirus type 1 (PCV-1) transcripts. Our aim was to identify novel RNA molecules and transcript isoforms, as well as to determine the exact 5'- and 3'-end sequences of previously described transcripts with single base-pair accuracy. We discovered a novel 3'-UTR length isoform of the Cap transcript, and a non-spliced Cap transcript variant. Additionally, our analysis has revealed a 3'-UTR isoform of Rep and two 5'-UTR isoforms of Rep' transcripts, and a novel splice variant of the longer Rep' transcript. We also explored two novel long transcripts, one with a previously identified splice site, and a formerly undetected mRNA of ORF3. Altogether, our methods have identified nine novel RNA molecules, doubling the size of PCV-1 transcriptome that had been known before. Additionally, our investigations revealed an intricate pattern of transcript overlapping, which might produce transcriptional interference between the transcriptional machineries of adjacent genes, and thereby may potentially play a role in the regulation of gene expression in circoviruses.

摘要

在本研究中,我们使用太平洋生物科学公司的RS II长读长测序技术和Illumina HiScanSQ短读长测序技术对1型猪圆环病毒(PCV-1)转录本进行表征。我们的目的是鉴定新的RNA分子和转录本异构体,以及以单碱基对精度确定先前描述的转录本的确切5'端和3'端序列。我们发现了Cap转录本的一种新的3'-UTR长度异构体和一种未剪接的Cap转录本变体。此外,我们的分析还揭示了Rep的一种3'-UTR异构体和Rep'转录本的两种5'-UTR异构体,以及较长Rep'转录本的一种新的剪接变体。我们还探索了两种新的长转录本,一种具有先前确定的剪接位点,以及一种以前未检测到的ORF3 mRNA。总之,我们的方法鉴定出了9种新的RNA分子,使之前已知的PCV-1转录组规模翻倍。此外,我们的研究揭示了一种复杂的转录本重叠模式,这可能会在相邻基因的转录机制之间产生转录干扰,从而可能在圆环病毒的基因表达调控中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8dd/5927800/46a3e87313b9/nihms952136f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8dd/5927800/88b7b1f59fe7/nihms952136f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8dd/5927800/7783e3930207/nihms952136f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8dd/5927800/b860866cb9d3/nihms952136f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8dd/5927800/76a98a2a8542/nihms952136f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8dd/5927800/19474bf82c9c/nihms952136f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8dd/5927800/f1276e0f0e0f/nihms952136f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8dd/5927800/46a3e87313b9/nihms952136f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8dd/5927800/88b7b1f59fe7/nihms952136f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8dd/5927800/7783e3930207/nihms952136f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8dd/5927800/b860866cb9d3/nihms952136f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8dd/5927800/76a98a2a8542/nihms952136f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8dd/5927800/19474bf82c9c/nihms952136f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8dd/5927800/f1276e0f0e0f/nihms952136f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8dd/5927800/46a3e87313b9/nihms952136f7.jpg

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