Evidence map›Paper›PMID 38014128›Full record

ArticlebioRxiv : the preprint server for biology2023

The mechanism of mRNA activation.

Riley C Gentry, Nicholas A Ide, Victoria M Comunale, Erik W Hartwick, Colin D Kinz-Thompson, Ruben L Gonzalez

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Riley C GentryDepartment of Biological Sciences, Columbia University, New York, NY, USA.
Nicholas A IdeDepartment of Biological Sciences, Columbia University, New York, NY, USA.
Victoria M ComunaleDepartment of Chemistry, Columbia University, New York, NY, USA.
Erik W HartwickDepartment of Chemistry, Columbia University, New York, NY, USA.
Colin D Kinz-ThompsonDepartment of Chemistry, Columbia University, New York, NY, USA.ORCID 0000-0002-2636-7893
Ruben L GonzalezDepartment of Chemistry, Columbia University, New York, NY, USA.ORCID 0000-0002-1344-5581

Funding

The Structural Dynamics of Translation InitiationR01GM084288 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI GONZALEZ, RUBEN L · 2009 to 2022
$4.4M
The mechanism and regulation of mRNA recruitment during eukaryotic translation initiationR01CA277727 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Ruben L Gonzalez · 2023 to 2026
$1.3M
The Conformational Dynamics of eIF5B During Ribosomal Subunit JoiningF32GM139360 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI HARTWICK, ERIK W · 2020 to 2022
$128k
NCI NIH HHS R01 CA277727NIGMS NIH HHS F32 GM139360NIGMS NIH HHS R01 GM084288
6 · The paper itself

Abstract

During translation initiation, messenger RNA molecules must be identified and activated for loading into a ribosome. In this rate-limiting step, the heterotrimeric protein eukaryotic initiation factor eIF4F must recognize and productively interact with the 7-methylguanosine cap at the 5' end of the messenger RNA and subsequently activate the message. Despite its fundamental, regulatory role in gene expression, the molecular events underlying cap recognition and messenger RNA activation remain mysterious. Here, we generate a unique, single-molecule fluorescence imaging system to interrogate the dynamics with which eIF4F discriminates productive and non-productive locations on full-length, native messenger RNA molecules. At the single-molecule level, we observe stochastic sampling of eIF4F along the length of the messenger RNA and identify allosteric communication between the eIF4F subunits which ultimately drive cap-recognition and subsequent activation of the message. Our experiments uncover novel functions for each subunit of eIF4F and we conclude by presenting a model for messenger RNA activation which precisely defines the composition of the activated message. This model provides a general framework for understanding how messenger RNA molecules may be discriminated from one another, and how other RNA-binding proteins may control the efficiency of translation initiation.

Identifiers

PMID38014128
PMCPMC10680758

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.