Evidence map›Paper›PMID 31387452›Full record

ArticleRNA biology2019

Alternatively spliced variants of the 5'-UTR of the ARPC2 mRNA regulate translation by an internal ribosome entry site (IRES) harboring a guanine-quadruplex motif.

Munir A Al-Zeer, Mariola Dutkiewicz, Annekathrin von Hacht, Denise Kreuzmann, Viola Röhrs, Jens Kurreck

Abstract read
In one paragraph

Article in RNA biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Current Practice in Bicistronic IRES Reporter Use: A Systematic Review.International journal of molecular sciences · 2021
    Pooled it
  2. Ins and outs of IRES elements: function and significance.Biochemical Society transactions · 2025
    Review
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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.

Munir A Al-ZeerInstitute of Biotechnology, Technische Universität Berlin , Berlin , Germany.ORCID 0000-0002-1700-9920
Mariola DutkiewiczInstitute of Bioorganic Chemistry, Polish Academy of Sciences , Poznan , Poland.ORCID 0000-0003-1098-0308
Annekathrin von HachtInstitute of Biotechnology, Technische Universität Berlin , Berlin , Germany.
Denise KreuzmannInstitute of Biotechnology, Technische Universität Berlin , Berlin , Germany.
Viola RöhrsInstitute of Biotechnology, Technische Universität Berlin , Berlin , Germany.
Jens KurreckInstitute of Biotechnology, Technische Universität Berlin , Berlin , Germany.ORCID 0000-0002-1469-0052

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The 5'-UTR of the actin-related protein 2/3 complex subunit 2 (ARPC2) mRNA exists in two variants. Using a bicistronic reporter construct, the present study demonstrates that the longer variant of the 5'-UTR harbours an internal ribosome entry site (IRES) which is lacking in the shorter one. Multiple control assays confirmed that only this variant promotes cap-independent translation. Furthermore, it includes a guanine-rich region that is capable of forming a guanine-quadruplex (G-quadruplex) structure which was found to contribute to the IRES activity. To investigate the cellular function of the IRES element, we determined the expression level of ARPC2 at various cell densities. At high cell density, the relative ARPC2 protein level increases, supporting the presumed function of IRES elements in driving the expression of certain genes under stressful conditions that compromise cap-dependent translation. Based on chemical probing experiments and computer-based predictions, we propose a structural model of the IRES element, which includes the G-quadruplex motif exposed from the central stem-loop element. Taken together, our study describes the functional relevance of two alternative 5'-UTR splice variants of the ARPC2 mRNA, one of which contains an IRES element with a G-quadruplex as a central motif, promoting translation under stressful cellular conditions.

Indexed as

Internal Ribosome Entry Sites5' Untranslated RegionsActin-Related Protein 2-3 ComplexAlternative SplicingCell CountG-QuadruplexesHEK293 CellsHumansMCF-7 CellsProtein BiosynthesisRNA, Messenger5' Untranslated RegionsActin-Related Protein 2-3 ComplexARPC2 protein, humanInternal Ribosome Entry SitesRNA, MessengerARPC2cap-independent translationchemical probingG-quadruplexinternal ribosome entry site

Identifiers

PMID31387452
PMCPMC6779386

What OpenQuestion holds

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Registered trials

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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.