Evidence map›Paper›PMID 17255934›Full record

ArticleThe EMBO journal2007

HCV and CSFV IRES domain II mediate eIF2 release during 80S ribosome assembly.

Nicolas Locker, Laura E Easton, Peter J Lukavsky

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The EMBO journal, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed, 1 pooled it
7.4field-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

95 citing papers in PubMed, 1 synthesis or guideline pooled it, 143 citations in OpenAlex.

  1. Pooled it
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  17. Hepatitis C Virus Translation Regulation.International journal of molecular sciences · 2020
    Review
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35 more citing papers are in PubMed but not listed here.

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.

Nicolas LockerMRC Laboratory of Molecular Biology, Hills Road, Cambridge CB2 2QH, UK.
Laura E Easton
Peter J Lukavsky
MRC Laboratory of Molecular Biology · GB

Funding

Medical Research Council MC_U105170649
6 · The paper itself

Abstract

Internal ribosome entry site (IRES) RNAs from the hepatitis C virus (HCV) and classical swine fever virus (CSFV) coordinate cap-independent assembly of eukaryotic 48S initiation complexes, consisting of the 40S ribosomal subunit, eukaryotic initiation factor (eIF) 3 and the eIF2/GTP/Met-tRNA(i)(Met) ternary complex. Here, we report that these IRESes also play a functional role during 80S ribosome assembly downstream of 48S complex formation, in promoting eIF5-induced GTP hydrolysis and eIF2/GDP release from the initiation complex. We show that this function is encoded in their independently folded IRES domain II and that it depends both on its characteristic bent conformation and two conserved RNA motifs, an apical hairpin loop and a loop E. Our data suggest a general mode of subunit joining in HCV and HCV-like IRESes.

Indexed as

Models, Molecular5' Untranslated RegionsBase PairingBase SequenceBlotting, NorthernClassical Swine Fever VirusEukaryotic Initiation Factor-2Eukaryotic Translation Initiation Factor 5AHepacivirusImmunoblottingMagnetic Resonance SpectroscopyMolecular Sequence DataPeptide Initiation FactorsProtein Structure, TertiaryRibosomesRNA-Binding Proteins5' Untranslated RegionsEukaryotic Initiation Factor-2Eukaryotic Translation Initiation Factor 5APeptide Initiation FactorsRNA-Binding Proteins

Identifiers

PMID17255934
PMCPMC1794401
OpenAlexW1984902027

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.