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Updated: Jan 2, 2026

Monitoring eIF4F Assembly by Measuring eIF4E-eIF4G Interaction in Live Cells
Published on: May 1, 2020
A novel eIF4E-interacting protein that forms non-canonical translation initiation complexes.
René Toribio1, Alfonso Muñoz1,2, Ana B Castro-Sanz1
1Centro de Biotecnología y Genómica de Plantas, Universidad Politécnica de Madrid (UPM) - Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA), Madrid, Spain.
Researchers discovered CERES, a novel plant protein that interacts with eukaryotic initiation factor 4E (eIF4E). CERES regulates translation, impacting gene expression and plant responses.
Area of Science:
- Molecular Biology
- Plant Science
- Gene Expression Regulation
Background:
- Translation initiation is crucial for gene expression and is regulated by protein interactions with eukaryotic initiation factor 4E (eIF4E).
- While eIF4E-binding proteins regulate translation in many eukaryotes, such factors were previously unidentified in plants.
Purpose of the Study:
- To identify and characterize novel plant proteins that interact with eIF4E and regulate translation.
- To elucidate the role of the newly discovered protein, CERES, in plant translation initiation.
Main Methods:
- Co-immunoprecipitation to identify eIF4E-interacting proteins.
- Analysis of protein domains (LRR) and binding sites.
- Biochemical assays to assess translation promotion in vitro.
- In vivo studies to evaluate effects on general and specific mRNA translation.
Main Results:
- Discovery of CERES, a plant eIF4E-interacting protein with an LRR domain and a canonical eIF4E-binding site.
- CERES forms part of cap-binding complexes and interacts with translation factors like eIF4A, PABP, and eIF3.
- CERES enhances translation in vitro and in vivo, modulating specific mRNA translation related to light and carbohydrate responses.
Conclusions:
- CERES functions as a non-canonical translation initiation factor in plants.
- This discovery provides new insights into the regulation of translation in plants, distinct from canonical pathways involving eIF4G.
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