Evidence map›Paper›PMID 22751931›Full record

ArticleMolecular and cellular biology2012

A novel 4EHP-GIGYF2 translational repressor complex is essential for mammalian development.

Masahiro Morita, Lian Wee Ler, Marc R Fabian, Nadeem Siddiqui, Michael Mullin, Valerie C Henderson, Tommy Alain, Bruno D Fonseca, Galina Karashchuk, Christopher F Bennett and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 118 papers.

0numbers the graph read from it
0cells of the map it votes in
118citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

118 citing papers in PubMed, 205 citations in OpenAlex.

  1. Review
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  10. Disrupted diencephalon development and neuropeptidergic pathways in zebrafish with autism-risk mutations.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  11. Review
  12. Article
  13. 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
    Article
  14. Article
  15. Review
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58 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

17 authors at 8 institutions in 4 countries.

Masahiro MoritaDepartment of Biochemistry and Goodman Cancer Research Centre, McGill University, Montréal, Quebec, Canada.
Lian Wee Ler
Marc R Fabian
Nadeem Siddiqui
Michael Mullin
Valerie C Henderson
Tommy Alain
Bruno D Fonseca
Galina Karashchuk
Christopher F Bennett
Tomohiro Kabuta
Shinji Higashi
Ola Larsson
Ivan Topisirovic
Robert J Smith
Anne-Claude Gingras
Nahum Sonenberg
McGill University Health Centre · CABrown University · USJewish General Hospital · CAKarolinska Institutet · SELunenfeld-Tanenbaum Research Institute · CAMount Sinai Hospital · CANational Center of Neurology and Psychiatry · JPTokyo Metropolitan Institute of Medical Science · JP

Funding

Canadian Institutes of Health Research MOP-84314
6 · The paper itself

Abstract

The binding of the eukaryotic initiation factor 4E (eIF4E) to the mRNA 5' cap structure is a rate-limiting step in mRNA translation initiation. eIF4E promotes ribosome recruitment to the mRNA. In Drosophila, the eIF4E homologous protein (d4EHP) forms a complex with binding partners to suppress the translation of distinct mRNAs by competing with eIF4E for binding the 5' cap structure. This repression mechanism is essential for the asymmetric distribution of proteins and normal embryonic development in Drosophila. In contrast, the physiological role of the mammalian 4EHP (m4EHP) was not known. In this study, we have identified the Grb10-interacting GYF protein 2 (GIGYF2) and the zinc finger protein 598 (ZNF598) as components of the m4EHP complex. GIGYF2 directly interacts with m4EHP, and this interaction is required for stabilization of both proteins. Disruption of the m4EHP-GIGYF2 complex leads to increased translation and perinatal lethality in mice. We propose a model by which the m4EHP-GIGYF2 complex represses translation of a subset of mRNAs during embryonic development, as was previously reported for d4EHP.

Indexed as

Protein BiosynthesisAmino Acid MotifsAnimalsCarrier ProteinsEmbryo, MammalianEukaryotic Initiation Factor-4EGene Expression Regulation, DevelopmentalHEK293 CellsHeLa CellsHumansMiceMice, KnockoutProtein BindingProtein Interaction Domains and MotifsProtein Interaction MapsCarrier ProteinsEukaryotic Initiation Factor-4EGIGYF2 protein, humanGIGYF2 protein, mouseZNF598 protein, human

Identifiers

PMID22751931
PMCPMC3422012
OpenAlexW2171632740

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.