Evidence map›Paper›PMID 33127640›Full record

ArticleThe Journal of biological chemistry2020

Molecular characterization of the RNA-protein complex directing -2/-1 programmed ribosomal frameshifting during arterivirus replicase expression.

Ankoor Patel, Emmely E Treffers, Markus Meier, Trushar R Patel, Jörg Stetefeld, Eric J Snijder, Brian L Mark

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Classification, replication, and transcription ofFrontiers in microbiology · 2023
    Review
  6. Viral evasion of PKR restriction by reprogramming cellular stress granules.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  7. Article
  8. Article
  9. Review
  10. 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

7 authors at 3 institutions in 2 countries.

Ankoor PatelDepartment of Microbiology, University of Manitoba, Winnipeg, Manitoba, Canada.
Emmely E TreffersMolecular Virology Laboratory, Department of Medical Microbiology, Leiden University Medical Center, Leiden, The Netherlands.
Markus MeierDepartment of Chemistry, University of Manitoba, Winnipeg, Manitoba, Canada.
Trushar R PatelAlberta RNA Research and Training Institute, Department of Chemistry and Biochemistry, University of Lethbridge, Lethbridge, Alberta, Canada.
Jörg StetefeldDepartment of Chemistry, University of Manitoba, Winnipeg, Manitoba, Canada.
Eric J SnijderMolecular Virology Laboratory, Department of Medical Microbiology, Leiden University Medical Center, Leiden, The Netherlands.
Brian L MarkDepartment of Microbiology, University of Manitoba, Winnipeg, Manitoba, Canada. Electronic address: brian.mark@umanitoba.ca.
University of Manitoba · CALeiden University Medical Center · NLUniversity of Lethbridge · CA

Funding

CIHR 201610PJT-152935
6 · The paper itself

Abstract

Programmed ribosomal frameshifting (PRF) is a mechanism used by arteriviruses like porcine reproductive and respiratory syndrome virus (PRRSV) to generate multiple proteins from overlapping reading frames within its RNA genome. PRRSV employs -1 PRF directed by RNA secondary and tertiary structures within its viral genome (canonical PRF), as well as a noncanonical -1 and -2 PRF that are stimulated by the interactions of PRRSV nonstructural protein 1β (nsp1β) and host protein poly(C)-binding protein (PCBP) 1 or 2 with the viral genome. Together, nsp1β and one of the PCBPs act as transactivators that bind a C-rich motif near the shift site to stimulate -1 and -2 PRF, thereby enabling the ribosome to generate two frameshift products that are implicated in viral immune evasion. How nsp1β and PCBP associate with the viral RNA genome remains unclear. Here, we describe the purification of the nsp1β:PCBP2:viral RNA complex on a scale sufficient for structural analysis using small-angle X-ray scattering and stochiometric analysis by analytical ultracentrifugation. The proteins associate with the RNA C-rich motif as a 1:1:1 complex. The monomeric form of nsp1β within the complex differs from previously reported homodimer identified by X-ray crystallography. Functional analysis of the complex via mutational analysis combined with RNA-binding assays and cell-based frameshifting reporter assays reveal a number of key residues within nsp1β and PCBP2 that are involved in complex formation and function. Our results suggest that nsp1β and PCBP2 both interact directly with viral RNA during formation of the complex to coordinate this unusual PRF mechanism.

Indexed as

Virus ReplicationAnimalsDNA-Binding ProteinsFrameshifting, RibosomalHost-Pathogen InteractionsHumansImmune EvasionPorcine Reproductive and Respiratory SyndromePorcine respiratory and reproductive syndrome virusRNA-Binding ProteinsRNA, ViralSwineViral Nonstructural ProteinsDNA-Binding ProteinsPCBP1 protein, humanRNA-Binding ProteinsRNA, ViralViral Nonstructural Proteinsnidovirusnonstructural protein 1nsp1nsp1betaPCBPPCPB2poly(C)-binding proteinPRRSVribosomeribosome functionRNARNA virussedimentation velocitysmall-angle X-ray scatteringstructural biologytranslationviral replicationvirologyβ

Identifiers

PMID33127640
PMCPMC7939443
OpenAlexW3094697422

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.