Long-Read Isoform Sequencing Reveals a Hidden Complexity of the Transcriptional Landscape of Herpes Simplex Virus Type 1

In this study, we used the amplified isoform sequencing technique from Pacific Biosciences to characterize the poly(A)+ fraction of the lytic transcriptome of the herpes simplex virus type 1 (HSV-1). Our analysis detected 34 formerly unidentified protein-coding genes, 10 non-coding RNAs, as well as 17 polycistronic and complex transcripts. This work also led us to identify many transcript isoforms, including 13 splice and 68 transcript end variants, as well as several transcript overlaps. Additionally, we determined previously unascertained transcriptional start and polyadenylation sites. We analyzed the transcriptional activity from the complementary DNA strand in five convergent HSV gene pairs with quantitative RT-PCR and detected antisense RNAs in each gene. This part of the study revealed an inverse correlation between the expressions of convergent partners. Our work adds new insights for understanding the complexity of the pervasive transcriptional overlaps by suggesting that there is a crosstalk between adjacent and distal genes through interaction between their transcription apparatuses. We also identified transcripts overlapping the HSV replication origins, which may indicate an interplay between the transcription and replication machineries. The relative abundance of HSV-1 transcripts has also been established by using a novel method based on the calculation of sequencing reads for the analysis.

[1]  Guoli Ji,et al.  Genome level analysis of rice mRNA 3′-end processing signals and alternative polyadenylation , 2008, Nucleic acids research.

[2]  Donald Sharon,et al.  Strain Kaplan of Pseudorabies Virus Genome Sequenced by PacBio Single-Molecule Real-Time Sequencing Technology , 2014, Genome Announcements.

[3]  A. Chenchik,et al.  Reverse transcriptase template switching: a SMART approach for full-length cDNA library construction. , 2001, BioTechniques.

[4]  K. Looker,et al.  Global and Regional Estimates of Prevalent and Incident Herpes Simplex Virus Type 1 Infections in 2012 , 2015, PloS one.

[5]  T. Block,et al.  Identification of a novel 0.7-kb polyadenylated transcript in the LAT promoter region of HSV-1 that is strain specific and may contribute to virulence. , 1999, Virology.

[6]  Thomas Bonfert,et al.  Widespread disruption of host transcription termination in HSV-1 infection , 2015, Nature Communications.

[7]  Shannon L. Risacher,et al.  Identifying disease sensitive and quantitative trait-relevant biomarkers from multidimensional heterogeneous imaging genetics data via sparse multimodal multitask learning , 2012, Bioinform..

[8]  Donald Sharon,et al.  Characterization of the Dynamic Transcriptome of a Herpesvirus with Long-read Single Molecule Real-Time Sequencing , 2017, Scientific Reports.

[9]  István Prazsák,et al.  Characterization of pseudorabies virus transcriptome by Illumina sequencing , 2015, BMC Microbiology.

[10]  L. J. Perry,et al.  The complete DNA sequence of the long unique region in the genome of herpes simplex virus type 1. , 1988, The Journal of general virology.

[11]  David J. Arenillas,et al.  JASPAR 2016: a major expansion and update of the open-access database of transcription factor binding profiles , 2015, Nucleic Acids Res..

[12]  Thomas D. Wu,et al.  GMAP: a genomic mapping and alignment program for mRNA and EST sequence , 2005, Bioinform..

[13]  Vladimir B. Bajic,et al.  Bioinformatics Applications Note Sequence Analysis Dragon Polya Spotter: Predictor of Poly(a) Motifs within Human Genomic Dna Sequences , 2022 .

[14]  Philip R. Cohen,et al.  Herpes simplex virus type 1 infections. , 1998, The Journal of the Greater Houston Dental Society.

[15]  S. McKnight The nucleotide sequence and transcript map of the herpes simplex virus thymidine kinase gene. , 1980, Nucleic acids research.

[16]  A. Strain,et al.  Herpes Simplex Virus Type 1 ICP27 Regulates Expression of a Variant, Secreted Form of Glycoprotein C by an Intron Retention Mechanism , 2008, Journal of Virology.

[17]  Yongxia Huo,et al.  Functional prediction of differentially expressed lncRNAs in HSV-1 infected human foreskin fibroblasts , 2016, Virology Journal.

[18]  H. Weintraub,et al.  Constitutive and conditional suppression of exogenous and endogenous genes by anti-sense RNA. , 1985, Science.

[19]  D. Long,et al.  Direct demonstration that the abundant 6-kilobase herpes simplex virus type 1 mRNA mapping between 0.23 and 0.27 map units encodes the major capsid protein VP5 , 1984, Journal of virology.

[20]  G. Edwalds-Gilbert,et al.  Alternative poly(A) site selection in complex transcription units: means to an end? , 1997, Nucleic acids research.

[21]  A. Nesburn,et al.  A Novel Herpes Simplex Virus Type 1 Transcript (AL-RNA) Antisense to the 5′ End of the Latency-Associated Transcript Produces a Protein in Infected Rabbits , 2002, Journal of Virology.

[22]  C. Thomas Caskey,et al.  Translational frameshifting: Where will it stop? , 1987, Cell.

[23]  B. Ely,et al.  Comparison of Genome Sequencing Technology and Assembly Methods for the Analysis of a GC-Rich Bacterial Genome , 2015, Current Microbiology.

[24]  Dóra Tombácz,et al.  Whole-genome analysis of pseudorabies virus gene expression by real-time quantitative RT-PCR assay , 2009, BMC Genomics.

[25]  F. Rixon,et al.  Detailed structural analysis of two spliced HSV-1 immediate-early mRNAs. , 1982, Nucleic acids research.

[26]  W. Merrick Cap-dependent and cap-independent translation in eukaryotic systems. , 2004, Gene.

[27]  Donald Sharon,et al.  Characterization of Novel Transcripts in Pseudorabies Virus , 2015, Viruses.

[28]  J. Mattick,et al.  Non-coding RNA. , 2006, Human molecular genetics.

[29]  Z. Boldogköi,et al.  Transcriptional interference networks coordinate the expression of functionally related genes clustered in the same genomic loci , 2012, Front. Gene..

[30]  C. Thompson,et al.  bcl-x, a bcl-2-related gene that functions as a dominant regulator of apoptotic cell death , 1993, Cell.

[31]  D. Rock,et al.  Localization of herpes simplex virus in the trigeminal and olfactory systems of the mouse central nervous system during acute and latent infections by in situ hybridization. , 1984, Laboratory investigation; a journal of technical methods and pathology.

[32]  P. Ghazal,et al.  Global Analysis of Herpes Simplex Virus Type 1 Transcription Using an Oligonucleotide-Based DNA Microarray , 2000, Journal of Virology.

[33]  L. Morrison,et al.  Genome Sequence of Herpes Simplex Virus 1 Strain KOS , 2012, Journal of Virology.

[34]  N. Fraser,et al.  Identification of a protein encoded in the herpes simplex virus type 1 latency associated transcript promoter region. , 2005, Virus research.

[35]  William Stafford Noble,et al.  FIMO: scanning for occurrences of a given motif , 2011, Bioinform..

[36]  F. Lim HSV-1 as a Model for Emerging Gene Delivery Vehicles , 2013 .

[37]  Vladimir B. Bajic,et al.  Dragon PolyA Spotter: predictor of poly(A) motifs within human genomic DNA sequences , 2011, Bioinform..

[38]  Frank Speleman,et al.  A novel and universal method for microRNA RT-qPCR data normalization , 2009, Genome Biology.

[39]  J. Mattick RNA regulation: a new genetics? , 2004, Nature Reviews Genetics.

[40]  Andrew J Davison,et al.  Topics in herpesvirus genomics and evolution. , 2006, Virus research.

[41]  B. Roizman,et al.  Properties of two 5'-coterminal RNAs transcribed part way and across the S component origin of DNA synthesis of the herpes simplex virus 1 genome. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[42]  B. Williams,et al.  Mapping and quantifying mammalian transcriptomes by RNA-Seq , 2008, Nature Methods.

[43]  Ben Lehner,et al.  Antisense transcripts in the human genome. , 2002, Trends in genetics : TIG.

[44]  Bernard Roizman,et al.  Patterns of accumulation of miRNAs encoded by herpes simplex virus during productive infection, latency, and on reactivation , 2014, Proceedings of the National Academy of Sciences.

[45]  D. Spector,et al.  Long noncoding RNAs: functional surprises from the RNA world. , 2009, Genes & development.

[46]  Glenn Tesler,et al.  Mapping single molecule sequencing reads using basic local alignment with successive refinement (BLASR): application and theory , 2012, BMC Bioinformatics.

[47]  Thomas E. Royce,et al.  Global Identification of Human Transcribed Sequences with Genome Tiling Arrays , 2004, Science.

[48]  Donald Sharon,et al.  A single-molecule long-read survey of the human transcriptome , 2013, Nature Biotechnology.

[49]  Eugene Bolotin,et al.  Prevalence of the initiator over the TATA box in human and yeast genes and identification of DNA motifs enriched in human TATA-less core promoters. , 2007, Gene.

[50]  E. Flemington,et al.  Global transcript structure resolution of high gene density genomes through multi-platform data integration , 2016, Nucleic acids research.

[51]  N. DeLuca,et al.  Transcription of the Herpes Simplex Virus 1 Genome during Productive and Quiescent Infection of Neuronal and Nonneuronal Cells , 2014, Journal of Virology.

[52]  N. Proudfoot Ending the message: poly(A) signals then and now. , 2011, Genes & development.

[53]  Nadav S. Bar,et al.  Landscape of transcription in human cells , 2012, Nature.

[54]  J. Rajčáni,et al.  Peculiarities of Herpes Simplex Virus (HSV) Transcription: An overview , 2004, Virus Genes.

[55]  Masahiro Kasahara,et al.  Performance comparison of second- and third-generation sequencers using a bacterial genome with two chromosomes , 2014, BMC Genomics.

[56]  Donald Sharon,et al.  Full-Length Isoform Sequencing Reveals Novel Transcripts and Substantial Transcriptional Overlaps in a Herpesvirus , 2016, PloS one.

[57]  M. Gerstein,et al.  RNA-Seq: a revolutionary tool for transcriptomics , 2009, Nature Reviews Genetics.

[58]  S. Batalov,et al.  Antisense Transcription in the Mammalian Transcriptome , 2005, Science.