Multiplatform next-generation sequencing identifies novel RNA molecules and transcript isoforms of the endogenous retrovirus isolated from cultured cells

FEMS Microbiol Lett. 2018 Mar 1;365(5):fny013. doi: 10.1093/femsle/fny013.

Abstract

In this study, we applied short- and long-read RNA sequencing techniques, as well as PCR analysis to investigate the transcriptome of the porcine endogenous retrovirus (PERV) expressed from cultured porcine kidney cell line PK-15. This analysis has revealed six novel transcripts and eight transcript isoforms, including five length and three splice variants. We were able to establish whether a deletion in a transcript is the result of the splicing of mRNAs or of genomic deletion in one of the PERV clones. Additionally, we re-annotated the formerly identified RNA molecules. Our analysis revealed a higher complexity of PERV transcriptome than it was earlier believed.

Keywords: Oxford Nanopore Technologies; Pacific Biosciences; RNA-Seq; endogenous retrovirus; full-length sequencing; transcriptome.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing
  • Animals
  • Cell Line
  • Endogenous Retroviruses / genetics*
  • Gene Expression Profiling
  • Genome, Viral / genetics
  • High-Throughput Nucleotide Sequencing
  • RNA, Messenger / genetics*
  • RNA, Viral / genetics*
  • Sequence Deletion
  • Swine

Substances

  • RNA, Messenger
  • RNA, Viral