Evidence map›Paper›PMID 23129811›Full record

ArticleMolecular and cellular biology2013

Nucleotide composition of cellular internal ribosome entry sites defines dependence on NF45 and predicts a posttranscriptional mitotic regulon.

Mame Daro Faye, Tyson E Graber, Peng Liu, Nehal Thakor, Stephen D Baird, Danielle Durie, Martin Holcik

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Article
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  4. IRES Trans-Acting Factors, Key Actors of the Stress Response.International journal of molecular sciences · 2019
    Review
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  18. Expression of NF45 correlates with malignant grade in gliomas and plays a pivotal role in tumor growth.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Article
  19. RNA-binding proteins impacting on internal initiation of translation.International journal of molecular sciences · 2013
    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

7 authors at 2 institutions in 1 country.

Mame Daro FayeApoptosis Research Centre, Children's Hospital of Eastern Ontario, and University of Ottawa, Ottawa, Ontario, Canada.
Tyson E Graber
Peng Liu
Nehal Thakor
Stephen D Baird
Danielle Durie
Martin Holcik
University of Ottawa · CAChildren's Hospital of Eastern Ontario · CA

Funding

Canadian Institutes of Health Research FRN 74740
6 · The paper itself

Abstract

The vast majority of cellular mRNAs initiate their translations through a well-defined mechanism of ribosome recruitment that occurs at the 5'-terminal 7-methylguanosine cap with the help of several canonical protein factors. A subset of cellular and viral mRNAs contain regulatory motifs in their 5' untranslated regions (UTRs), termed internal ribosome entry sites (IRES), that sidestep this canonical mode of initiation. On cellular mRNAs, this mechanism requires IRES trans-acting protein factors (ITAFs) that facilitate ribosome recruitment downstream of the cap. While several ITAFs and their target mRNAs have been empirically identified, the in silico prediction of targets has proved difficult. Here, we report that a high AU content (>60%) of the IRES-containing 5' UTRs serves as an excellent predictor of dependence on NF45, a recently identified ITAF. Moreover, we provide evidence that cells deficient in NF45 ITAF activity exhibit reduced IRES-mediated translation of X-linked inhibitor of apoptosis protein (XIAP) and cellular inhibitor of apoptosis protein 1 (cIAP1) mRNAs that, in turn, leads to dysregulated expression of their respective targets, survivin and cyclin E. This specific defect in IRES translation explains in part the cytokinesis impairment and senescence-like phenotype observed in HeLa cells expressing NF45 RNA interference (RNAi). This study uncovers a novel role for NF45 in regulating ploidy and highlights the importance of IRES-mediated translation in cellular homeostasis.

Indexed as

Cellular SenescenceMitosis5' Untranslated RegionsCell ProliferationCloning, MolecularCyclin EGene Expression RegulationHeLa CellsHumansImmunoprecipitationInhibitor of Apoptosis ProteinsMicroscopy, FluorescenceNuclear Factor 45 ProteinNucleotidesPhenotypeRegulon5' Untranslated RegionsBIRC5 protein, humanCyclin EILF2 protein, humanInhibitor of Apoptosis ProteinsNuclear Factor 45 ProteinNucleotidesRNA, MessengerSurvivinXIAP protein, humanX-Linked Inhibitor of Apoptosis Protein

Identifiers

PMID23129811
PMCPMC3554113
OpenAlexW2121187425

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.