Evidence map›Paper›PMID 33758928›Full record

ArticleNucleic acids research2021

microRNA-mediated translation repression through GYF-1 and IFE-4 in C. elegans development.

Vinay K Mayya, Mathieu N Flamand, Alice M Lambert, Seyed Mehdi Jafarnejad, James A Wohlschlegel, Nahum Sonenberg, Thomas F Duchaine

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.7field-weighted citation impact, top 5% 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

21 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
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  4. The 4EHP-mediated translational repression of cGAS impedes the host immune response against DNA viruses.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  16. SARS-CoV-2 impairs interferon production via NSP2-induced repression of mRNA translation.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  17. Article
  18. Article
  19. Eukaryotic mRNA Decapping Activation.Frontiers in genetics · 2022
    Review
  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

7 authors at 3 institutions in 3 countries.

Vinay K MayyaGoodman Cancer Research Center, McGill University, Montréal H3G 1Y6, Canada.
Mathieu N FlamandGoodman Cancer Research Center, McGill University, Montréal H3G 1Y6, Canada.
Alice M LambertGoodman Cancer Research Center, McGill University, Montréal H3G 1Y6, Canada.
Seyed Mehdi JafarnejadPatrick G. Johnston Centre for Cancer Research, Queen's University of Belfast, Belfast BT9 7AE UK.
James A WohlschlegelDepartment of Biological Chemistry, David Geffen School of Medicine, University of California, Los Angeles, CA 90095, USA.
Nahum SonenbergGoodman Cancer Research Center, McGill University, Montréal H3G 1Y6, Canada.
Thomas F DuchaineGoodman Cancer Research Center, McGill University, Montréal H3G 1Y6, Canada.ORCID 0000-0002-3454-1839
McGill University · CAQueen's University Belfast · GBUniversity of California, Los Angeles · US

Funding

Proteolytic Control of Iron Metabolism by the Ubiquitin Ligase FBXL5R01GM089778 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WOHLSCHLEGEL, JAMES AKIRA · 2010 to 2023
$4.0M
CIHR MOP-123352NIGMS NIH HHS R01 GM089778
6 · The paper itself

Abstract

microRNA (miRNA)-mediated gene silencing is enacted through the recruitment of effector proteins that direct translational repression or degradation of mRNA targets, but the relative importance of their activities for animal development remains unknown. Our concerted proteomic surveys identified the uncharacterized GYF-domain encoding protein GYF-1 and its direct interaction with IFE-4, the ortholog of the mammalian translation repressor 4EHP, as key miRNA effector proteins in Caenorhabditis elegans. Recruitment of GYF-1 protein to mRNA reporters in vitro or in vivo leads to potent translation repression without affecting the poly(A) tail or impinging on mRNA stability. Loss of gyf-1 is synthetic lethal with hypomorphic alleles of embryonic miR-35-42 and larval (L4) let-7 miRNAs, which is phenocopied through engineered mutations in gyf-1 that abolish interaction with IFE-4. GYF-1/4EHP function is cascade-specific, as loss of gyf-1 had no noticeable impact on the functions of other miRNAs, including lin-4 and lsy-6. Overall, our findings reveal the first direct effector of miRNA-mediated translational repression in C. elegans and its physiological importance for the function of several, but likely not all miRNAs.

Indexed as

Gene Expression Regulation, DevelopmentalGene SilencingProtein BiosynthesisAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsEukaryotic Initiation Factor-4EGenes, LethalMicroRNAsProtein DomainsProteomicsRNA-Induced Silencing ComplexCaenorhabditis elegans ProteinsEukaryotic Initiation Factor-4Elet-7 microRNA, C elegansMicroRNAsMIRN35 microRNA, C elegansRNA-Induced Silencing Complex

Identifiers

PMID33758928
PMCPMC8136787
OpenAlexW3138249613

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.