» Articles » PMID: 24692447

RNA Structures That Resist Degradation by Xrn1 Produce a Pathogenic Dengue Virus RNA

Overview
Journal Elife
Specialty Biology
Date 2014 Apr 3
PMID 24692447
Citations 126
Authors
Affiliations
Soon will be listed here.
Abstract

Dengue virus is a growing global health threat. Dengue and other flaviviruses commandeer the host cell's RNA degradation machinery to generate the small flaviviral RNA (sfRNA), a noncoding RNA that induces cytopathicity and pathogenesis. Host cell exonuclease Xrn1 likely loads on the 5' end of viral genomic RNA and degrades processively through ∼10 kB of RNA, halting near the 3' end of the viral RNA. The surviving RNA is the sfRNA. We interrogated the architecture of the complete Dengue 2 sfRNA, identifying five independently-folded RNA structures, two of which quantitatively confer Xrn1 resistance. We developed an assay for real-time monitoring of Xrn1 resistance that we used with mutagenesis and RNA folding experiments to show that Xrn1-resistant RNAs adopt a specific fold organized around a three-way junction. Disrupting the junction's fold eliminates the buildup of disease-related sfRNAs in human cells infected with a flavivirus, directly linking RNA structure to sfRNA production. DOI: http://dx.doi.org/10.7554/eLife.01892.001.

Citing Articles

The zinc finger protein ZFP36L2 inhibits flavivirus infection via the 5'-3' XRN1-mediated RNA decay pathway in the replication complexes.

Lin R, Lin L, Chen Z, Liu B, Ko P, Liao C J Biomed Sci. 2025; 32(1):27.

PMID: 39972499 PMC: 11841009. DOI: 10.1186/s12929-025-01122-0.


Lifetime of ground conformational state determines the activity of structured RNA.

Thompson R, Carbaugh D, Nielsen J, Witt C, Faison E, Meganck R Nat Chem Biol. 2025; .

PMID: 39939412 DOI: 10.1038/s41589-025-01843-1.


The pseudoknot structure of a viral RNA reveals a conserved mechanism for programmed exoribonuclease resistance.

Gezelle J, Korn S, McDonald J, Gong Z, Erickson A, Huang C bioRxiv. 2025; .

PMID: 39763890 PMC: 11702639. DOI: 10.1101/2024.12.17.628992.


Selectively expressed RNA molecules as a versatile tool for functionalized cell targeting.

Rastfeld F, Hoffmann M, Kruger S, Bohn P, Gribling-Burrer A, Wagner L Nat Commun. 2025; 16(1):420.

PMID: 39762287 PMC: 11704337. DOI: 10.1038/s41467-024-55547-6.


Purification of Enzymatically Active Xrn1 for Removal of Non-capped mRNAs from In Vitro Transcription Reactions and Evaluation of mRNA Decapping Status In Vivo.

Drazkowska K, Tomecki R, Tudek A Methods Mol Biol. 2024; 2863:81-105.

PMID: 39535706 DOI: 10.1007/978-1-0716-4176-7_7.


References
1.
Sztuba-Solinska J, Teramoto T, Rausch J, Shapiro B, Padmanabhan R, Le Grice S . Structural complexity of Dengue virus untranslated regions: cis-acting RNA motifs and pseudoknot interactions modulating functionality of the viral genome. Nucleic Acids Res. 2013; 41(9):5075-89. PMC: 3643606. DOI: 10.1093/nar/gkt203. View

2.
Silva P, Pereira C, Dalebout T, Spaan W, Bredenbeek P . An RNA pseudoknot is required for production of yellow fever virus subgenomic RNA by the host nuclease XRN1. J Virol. 2010; 84(21):11395-406. PMC: 2953177. DOI: 10.1128/JVI.01047-10. View

3.
Woodson S, Koculi E . Analysis of RNA folding by native polyacrylamide gel electrophoresis. Methods Enzymol. 2010; 469:189-208. PMC: 6343852. DOI: 10.1016/S0076-6879(09)69009-1. View

4.
Bhatt S, Gething P, Brady O, Messina J, Farlow A, Moyes C . The global distribution and burden of dengue. Nature. 2013; 496(7446):504-7. PMC: 3651993. DOI: 10.1038/nature12060. View

5.
Villordo S, Gamarnik A . Genome cyclization as strategy for flavivirus RNA replication. Virus Res. 2008; 139(2):230-9. PMC: 5440119. DOI: 10.1016/j.virusres.2008.07.016. View