Evidence map›Paper›PMID 42327168›Full record

ArticlebioRxiv : the preprint server for biology2026

A ribosomal kinetic checkpoint governs selective mRNA recruitment.

Masaaki Sokabe, Carlos Alvarado, Christopher P Lapointe, Nancy Villa, Joseph D Puglisi, Christopher S Fraser

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. 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

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.

Masaaki SokabeDepartment of Molecular and Cellular Biology, College of Biological Sciences, University of California, Davis, CA, USA.ORCID 0000-0002-1824-4818
Carlos AlvaradoDepartment of Structural Biology, Stanford University School of Medicine, Stanford, CA, USA.
Christopher P LapointeBasic Sciences Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.ORCID 0000-0002-0406-105X
Nancy VillaDepartment of Molecular and Cellular Biology, College of Biological Sciences, University of California, Davis, CA, USA.ORCID 0009-0007-7095-1468
Joseph D PuglisiDepartment of Structural Biology, Stanford University School of Medicine, Stanford, CA, USA.
Christopher S FraserDepartment of Molecular and Cellular Biology, College of Biological Sciences, University of California, Davis, CA, USA.ORCID 0000-0001-9626-7743

Funding

Dynamics of TranslationR35GM145306 · NIGMS · STANFORD UNIVERSITY · PI JOSEPH D PUGLISI · 2022 to 2026
$3.8M
Defining modifiers and mechanisms of RAN translationR01AG064690 · NIA · STANFORD UNIVERSITY · PI Aaron D. Gitler, JOSEPH D PUGLISI · 2024 to 2026
$2.3M
The mechanisms of mRNA recruitment to the human ribosomeR35GM152137 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Christopher S Fraser · 2024 to 2026
$1.3M
From one end to the other: dynamics of human translation initiation and its controlK99GM144678 · NIGMS · STANFORD UNIVERSITY · PI LAPOINTE, CHRISTOPHER PAUL · 2022 to 2023
$164k
NIA NIH HHS R01 AG064690NIGMS NIH HHS K99 GM144678NIGMS NIH HHS R35 GM145306NIGMS NIH HHS R35 GM152137
6 · The paper itself

Abstract

Translation initiation begins with recruitment of mRNA to the ribosome, yet how mRNA engagement is converted into productive initiation remains unclear. Using real-time fluorescence assays with purified components, we show that mRNA recruitment proceeds through a branched kinetic pathway on the 40S subunit. Following rapid sampling, mRNAs partition into either a productive accommodated state or an arrested state that stabilizes ribosome binding before accommodation. mRNA structure, eIF3, and eIF3j bias recruitment toward arrest, whereas eIF4F promotes accommodation in an ATP-dependent manner coupled to displacement of eIF3j from the mRNA entry channel. Unstructured mRNAs accommodate independently of eIF4E, whereas structured mRNAs require an upstream eIF4E-dependent step, enabling selective recruitment under limiting eIF4E. Arrested complexes can convert directly into the accommodated state without dissociation, revealing a reversible standby intermediate poised for activation. Together, our findings establish mRNA accommodation as a ribosome-intrinsic checkpoint governing initiation and provide a framework for selective translation.

Identifiers

PMID42327168
PMCPMC13277876

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.