Evidence map›Paper›PMID 12773554›Full record

ArticleMolecular and cellular biology2003

Yeast Lsm1p-7p/Pat1p deadenylation-dependent mRNA-decapping factors are required for brome mosaic virus genomic RNA translation.

Amine O Noueiry, Juana Diez, Shaun P Falk, Jianbo Chen, Paul Ahlquist

Abstract read
In one paragraph

Article in Molecular and cellular biology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
9.2field-weighted citation impact, top 2% 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

56 citing papers in PubMed, 93 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. The function of chloroplast ferredoxin-NADPMolecular plant pathology · 2022
    Article
  5. Contribution of yeast models to virus research.Applied microbiology and biotechnology · 2021
    Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Hunting Viral Receptors Using Haploid Cells.Annual review of virology · 2015
    Review
  13. Article
  14. Article
  15. Cytoplasmic RNA Granules and Viral Infection.Annual review of virology · 2014
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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

5 authors at 3 institutions in 3 countries.

Amine O NoueiryInstitute for Molecular Virology. Howard Hughes Medical Institute, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.
Juana Diez
Shaun P Falk
Jianbo Chen
Paul Ahlquist
Institute of Virology of the Slovak Academy of Sciences · SKHoward Hughes Medical Institute · USPompeu Fabra University · ES

Funding

GENE FUNCTIONS AND MOLECULAR GENETICS OF RNA VIRUSESR37GM035072 · NIGMS · UNIVERSITY OF WISCONSIN MADISON · PI AHLQUIST, PAUL G. · 1995 to 2004
$1.9M
GENE FUNCTIONS AND MOLECULAR GENETICS OF RNA VIRUSESR01GM035072 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI AHLQUIST, PAUL G. · 1985 to 2009
$1.6M
NIGMS NIH HHS GM35072NIGMS NIH HHS R01 GM035072NIGMS NIH HHS R37 GM035072
6 · The paper itself

Abstract

Previously, we used the ability of the higher eukaryotic positive-strand RNA virus brome mosaic virus (BMV) to replicate in yeast to show that the yeast LSM1 gene is required for recruiting BMV RNA from translation to replication. Here we extend this observation to show that Lsm1p and other components of the Lsm1p-Lsm7p/Pat1p deadenylation-dependent mRNA decapping complex were also required for translating BMV RNAs. Inhibition of BMV RNA translation was selective, with no effect on general cellular translation. We show that viral genomic RNAs suitable for RNA replication were already distinguished from nonreplication templates at translation, well before RNA recruitment to replication. Among mRNA turnover pathways, only factors specific for deadenylated mRNA decapping were required for BMV RNA translation. Dependence on these factors was not only a consequence of the nonpolyadenylated nature of BMV RNAs but also involved the combined effects of the viral 5' and 3' noncoding regions and 2a polymerase open reading frame. High-resolution sucrose density gradient analysis showed that, while mutating factors in the Lsm1p-7p/Pat1p complex completely inhibited viral RNA translation, the levels of viral RNA associated with ribosomes were only slightly reduced in mutant yeast. This polysome association was further verified by using a conditional allele of essential translation initiation factor PRT1, which markedly decreased polysome association of viral genomic RNA in the presence or absence of an LSM7 mutation. Together, these results show that a defective Lsm1p-7p/Pat1p complex inhibits BMV RNA translation primarily by stalling or slowing the elongation of ribosomes along the viral open reading frame. Thus, factors in the Lsm1p-7p/Pat1p complex function not only in mRNA decapping but also in translation, and both translation and recruitment of BMV RNAs to viral RNA replication are regulated by a cell pathway that transfers mRNAs from translation to degradation.

Indexed as

Blotting, NorthernBlotting, WesternBromovirusCell DivisionDNA-Binding ProteinsMethyltransferasesModels, GeneticOpen Reading FramesProtein BiosynthesisRibosomesRNARNA-Binding ProteinsRNA Cap-Binding ProteinsRNA, MessengerSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsDNA-Binding ProteinsLSM1 protein, S cerevisiaeMethyltransferasesPAT1 protein, S cerevisiaeRNARNA-Binding ProteinsRNA Cap-Binding ProteinsRNA, MessengerSaccharomyces cerevisiae Proteins

Identifiers

PMID12773554
PMCPMC156131
OpenAlexW2127712903

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.