Evidence map›Paper›PMID 23272212›Full record

ArticlePloS one2012

Translation directed by hepatitis A virus IRES in the absence of active eIF4F complex and eIF2.

Natalia Redondo, Miguel Angel Sanz, Jutta Steinberger, Tim Skern, Yuri Kusov, Luis Carrasco

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Hepatitis A: Viral Structure, Classification, Life Cycle, Clinical Symptoms, Diagnosis Error, and Vaccination.The Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale · 2023
    Review
  5. Review
  6. Cellular cap-binding protein, eIF4E, promotes picornavirus genome restructuring and translation.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  7. Viral and cellular mRNA-specific activators harness PABP and eIF4G to promote translation initiation downstream of cap binding.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  8. Article
  9. Article
  10. Article
  11. Direct-acting Antivirals and Host-targeting Agents against the Hepatitis A Virus.Journal of clinical and translational hepatology · 2015
    Review
  12. Article
  13. Review
  14. Article
  15. RNA-binding proteins impacting on internal initiation of translation.International journal of molecular sciences · 2013
    Review
  16. Article
  17. Novel viral translation strategies.Wiley interdisciplinary reviews. RNA
    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

6 authors at 4 institutions in 3 countries.

Natalia RedondoCentro de Biologia Molecular Severo Ochoa (Consejo Superior de Investigaciones Científicas-Universidad Autónoma de Madrid), Madrid, Spain. nsevillano@cbm.uam.es
Miguel Angel Sanz
Jutta Steinberger
Tim Skern
Yuri Kusov
Luis Carrasco
Consejo Superior de Investigaciones Científicas · ESMax Perutz Labs · ATCentro de Biología Molecular Severo Ochoa · ESUniversity of Lübeck · DE

Funding

Austrian Science Fund FWF P 24038
6 · The paper itself

Abstract

Translation directed by several picornavirus IRES elements can usually take place after cleavage of eIF4G by picornavirus proteases 2A(pro) or L(pro). The hepatitis A virus (HAV) IRES is thought to be an exception to this rule because it requires intact eIF4F complex for translation. In line with previous results we report that poliovirus (PV) 2A(pro) strongly blocks protein synthesis directed by HAV IRES. However, in contrast to previous findings we now demonstrate that eIF4G cleavage by foot-and-mouth disease virus (FMDV) L(pro) strongly stimulates HAV IRES-driven translation. Thus, this is the first observation that 2A(pro) and L(pro) exhibit opposite effects to what was previously thought to be the case in HAV IRES. This effect has been observed both in hamster BHK and human hepatoma Huh7 cells. In addition, this stimulation of translation is also observed in cell free systems after addition of purified L(pro). Notably, in presence of this FMDV protease, translation directed by HAV IRES takes place when eIF2α has been inactivated by phosphorylation. Our present findings clearly demonstrate that protein synthesis directed by HAV IRES can occur when eIF4G has been cleaved and after inactivation of eIF2. Therefore, translation directed by HAV IRES without intact eIF4G and active eIF2 is similar to that observed with other picornavirus IRESs.

Indexed as

Protein BiosynthesisRNA, Viral5' Untranslated RegionsAnimalsCell-Free SystemCell LineCricetinaeEukaryotic Initiation Factor-2Eukaryotic Initiation Factor-4FFoot-and-Mouth Disease VirusHepatitis A virusHumansPoliovirusProteolysisRNA, MessengerTransfection5' Untranslated RegionsEukaryotic Initiation Factor-2Eukaryotic Initiation Factor-4FRNA, MessengerRNA, Viral

Identifiers

PMID23272212
PMCPMC3525551
OpenAlexW2048384310

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.