Evidence map›Paper›PMID 40291665›Full record

ArticlebioRxiv : the preprint server for biology2025

Deaminase-based RNA recording enables high throughput mutational profiling of protein-RNA interactions.

Rachael A Bakker, Oliver B Nicholson, Heungwon Park, Yu-Lan Xiao, Weixin Tang, Arvind Rasi Subramaniam, Christopher P Lapointe

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

7 authors.

Rachael A BakkerBasic Sciences Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.
Oliver B NicholsonBasic Sciences Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.
Heungwon ParkBasic Sciences Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.
Yu-Lan XiaoDepartment of Chemistry and Institute for Biophysical Dynamics, The University of Chicago, Chicago, IL 60637, USA.
Weixin TangDepartment of Chemistry and Institute for Biophysical Dynamics, The University of Chicago, Chicago, IL 60637, USA.
Arvind Rasi SubramaniamBasic Sciences Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.ORCID 0000-0001-6145-4303
Christopher P LapointeBasic Sciences Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.ORCID 0000-0002-0406-105X

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
Regulation of Protein Synthesis by Synonymous Codon UsageR35GM119835 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI SUBRAMANIAM, ARVIND RASI · 2016 to 2025
$4.1M
High-Performance Compute Cluster for Comprehensive Cancer and Infectious Diseases ResearchS10OD028685 · OD · FRED HUTCHINSON CANCER RESEARCH CENTER · PI BRADLEY, PHILIP · 2020 to 2020
$2.0M
FHCRC High-Performance Computing ClusterS10OD020069 · OD · FRED HUTCHINSON CANCER RESEARCH CENTER · PI KOOPERBERG, CHARLES L · 2015 to 2015
$600k
From one end to the other: dynamics of human translation initiation and its controlR00GM144678 · NIGMS · FRED HUTCHINSON CANCER CENTER · PI LAPOINTE, CHRISTOPHER PAUL · 2023 to 2024
$498k
NCI NIH HHS P30 CA015704NIGMS NIH HHS R00 GM144678NIGMS NIH HHS R35 GM119835NIH HHS S10 OD020069NIH HHS S10 OD028685
6 · The paper itself

Abstract

Protein-RNA interactions govern nearly every aspect of RNA metabolism and are frequently dysregulated in disease. While individual protein residues and RNA nucleotides critical for these interactions have been characterized, scalable methods that jointly map protein- and RNA-level determinants remain limited. RNA deaminase fusions have emerged as a powerful strategy to identify transcriptome-wide targets of RNA-binding proteins by converting binding events into site-specific nucleotide edits. Here, we demonstrate that this 'RNA recording' approach enables high-throughput mutational scanning of protein-RNA interfaces. Using the λN-boxB system as a model, we show that editing by a fused TadA adenosine deaminase directly correlates with binding affinity between protein and RNA variants

Identifiers

PMID40291665
PMCPMC12027372

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.