Evidence map›Paper›PMID 29118186›Full record

ArticleThe Journal of biological chemistry2018

Identification of phlebovirus and arenavirus RNA sequences that stall and repress the exoribonuclease XRN1.

Phillida A Charley, Carol J Wilusz, Jeffrey Wilusz

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.4field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Shared properties and singularities of exoribonuclease-resistant RNAs in viruses.Computational and structural biotechnology journal · 2021
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Colocalization of mACS central science · 2019
    Review
  18. Article
  19. A recap of RNA recapping.Wiley interdisciplinary reviews. RNA · 2019
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Phillida A CharleyDepartment of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, Colorado 80523.
Carol J WiluszDepartment of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, Colorado 80523.
Jeffrey WiluszDepartment of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, Colorado 80523. Electronic address: jeffrey.wilusz@colostate.edu.
Colorado State University · US

Funding

Flavivirus non-coding RNAs and the Host mRNA Decay MachineryR01AI123136 · NIAID · COLORADO STATE UNIVERSITY · PI WILUSZ, JEFFREY · 2016 to 2020
$1.9M
NIAID NIH HHS R01 AI123136
6 · The paper itself

Abstract

Regulated mRNA decay plays a vital role in determining both the level and quality of cellular gene expression. Viral RNAs must successfully evade this host RNA decay machinery to establish a productive infection. One way for RNA viruses to accomplish this is to target the cellular exoribonuclease XRN1, because this enzyme is accessible in the cytoplasm and plays a major role in mRNA decay. Members of the Flaviviridae use RNA structures in their 5'- or 3'-untranslated regions to stall and repress XRN1, effectively stabilizing viral RNAs while also causing significant dysregulation of host cell mRNA stability. Here, we use a series of biochemical assays to demonstrate that the 3'-terminal portion of the nucleocapsid (N) mRNA of Rift Valley fever virus, a phlebovirus of the Bunyaviridae family, also can effectively stall and repress XRN1. The region responsible for impeding XRN1 includes a G-rich portion that likely forms a G-quadruplex structure. The 3'-terminal portions of ambisense-derived transcripts of multiple arenaviruses also stalled XRN1. Therefore, we conclude that RNAs from two additional families of mammalian RNA viruses stall and repress XRN1. This observation. emphasizes the importance and commonality of this viral strategy to interfere with the 5'-to-3'-exoribonuclease component of the cytoplasmic RNA decay machinery.

Indexed as

3' Untranslated RegionsExoribonucleasesHEK293 CellsHeLa CellsHost-Pathogen InteractionsHumansMicrotubule-Associated ProteinsPhlebovirusRift Valley fever virusRNA, MessengerRNA StabilityRNA, ViralSequence Analysis, RNA3' Untranslated RegionsExoribonucleasesMicrotubule-Associated ProteinsRNA, MessengerRNA, ViralXRN1 protein, humanRNARNA degradationRNA turnoverRNA virusviral transcription

Identifiers

PMID29118186
PMCPMC5766927
OpenAlexW2767617241

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.