Identification of conserved, primary sequence motifs that direct retrovirus RNA fate

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

Precise stoichiometry of genome-length transcripts and alternatively spliced mRNAs is a hallmark of retroviruses. We discovered short, guanosine and adenosine sequence motifs in the 5untranslated region of several retroviruses and ascertained the reasons for their conservation using a representative lentivirus and genetically simpler retrovirus. We conducted site-directed mutagenesis of the GA-motifs in HIV molecular clones and observed steep replication delays in T-cells. Quantitative RNA analyses demonstrate the GA-motifs are necessary to retain unspliced viral transcripts from alternative splicing. Mutagenesis of the GA-motifs in a C-type retrovirus validate the similar downregulation of unspliced transcripts and virion structural protein. The evidence from cell-based co-precipitation studies shows the GA-motifs in the 5untranslated region confer binding by SFPQ/PSF, a protein co-regulated with T-cell activation. Diminished SFPQ/PSF or mutation of either GA-motif attenuates the replication of HIV. The interaction of SFPQ/PSF with both GA-motifs is crucial for maintaining the stoichiometry of the viral transcripts and does not affect packaging of HIV RNA. Our results demonstrate the conserved GA-motifs direct the fate of retrovirus RNA. These findings have exposed an RNA-based molecular target to attenuate retrovirus replication.

Original languageEnglish (US)
Pages (from-to)7366-7378
Number of pages13
JournalNucleic Acids Research
Volume46
Issue number14
Early online dateMay 26 2018
DOIs
StatePublished - Aug 21 2018

Bibliographical note

Funding Information:
National Institutes of Health [R01 CA108882 and P50GM103297]. Funding for open access charge: University of Minnesota funds (to K.B.L.). Conflict of interest statement. None declared.

Funding Information:
National Institutes of Health [R01 CA108882 and P50GM103297]. Funding for open access charge: University of Minnesota funds (to K.B.L.).

Publisher Copyright:
© The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research.

Keywords

  • SFPQ/PSF
  • Gene expression regulation
  • RNA gene regulation
  • RNA binding protein
  • RNA secondary structure

PubMed: MeSH publication types

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

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