Third-generation Sequencing Reveals Extensive Polycistronism and Transcriptional Overlapping in a Baculovirus

被引:38
|
作者
Moldovan, Norbert [1 ]
Tombacz, Dora [1 ]
Szucs, Attila [1 ]
Csabai, Zsolt [1 ]
Balazs, Zsolt [1 ]
Kis, Emese [2 ]
Molnar, Judit [2 ]
Boldogkoi, Zsolt [1 ]
机构
[1] Univ Szeged, Dept Med Biol, Fac Med, H-6720 Szeged, Hungary
[2] Solvo Biotechnol, H-6720 Szeged, Hungary
来源
SCIENTIFIC REPORTS | 2018年 / 8卷
关键词
CALIFORNICA MULTIPLE NUCLEOPOLYHEDROVIRUS; MESSENGER-RNA; TRANSLATION; DNA; REPLICATION; COMPLEXITY; MECHANISM; NANOPORE; PROGRAM;
D O I
10.1038/s41598-018-26955-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Autographa californica multiple nucleopolyhedrovirus (AcMNPV) is an insect-pathogen baculovirus. In this study, we applied the Oxford NanoporeTechnologies platform for the analysis of the polyadenylated fraction of the viral transcriptome using both cDNA and direct RNA sequencing methods. We identified and annotated altogether 132 novel transcripts and transcript isoforms, including 4 coding and 4 non-coding RNA molecules, 47 length variants, 5 splice isoforms, as well as 23 polycistronic and 49 complex transcripts. All of the identified novel protein-coding genes were 5'-truncated forms of longer host genes. In this work, we demonstrated that in the case of transcript start site isoforms, the promoters and the initiator sequence of the longer and shorter variants belong to the same kinetic class. Long-read sequencing also revealed a complex meshwork of transcriptional overlaps, the function of which needs to be clarified. Additionally, we developed bioinformatics methods to improve the transcript annotation and to eliminate the non-specific transcription reads generated by template switching and false priming.
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页数:11
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