Evidence map›Paper›PMID 42897178›Full record

ArticleNature communications2026

The PAXT connection is a modifier of rare codon-enriched protein expression.

Taylor Niehoff, Jackson Peterson, Siqi Li, Sijin Chen, Christopher V Nicchitta, Alain Laederach, Christopher M Counter

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Taylor NiehoffDepartment of Pharmacology & Cancer Biology, Duke University Medical Center, Durham, NC, USA.ORCID 0000-0002-0506-6012
Jackson PetersonDepartment of Pharmacology & Cancer Biology, Duke University Medical Center, Durham, NC, USA.
Siqi LiDepartment of Pharmacology & Cancer Biology, Duke University Medical Center, Durham, NC, USA.
Sijin ChenDepartment of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.ORCID 0009-0006-3511-9919
Christopher V NicchittaDepartment of Cell Biology, Duke University Medical Center, Durham, NC, USA.ORCID 0000-0001-7889-1155
Alain LaederachDepartment of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Christopher M CounterDepartment of Pharmacology & Cancer Biology, Duke University Medical Center, Durham, NC, USA. count004@mc.duke.edu.ORCID 0000-0003-0748-3079

Funding

Non-coding RNA structure change in Chronic Obstructive Pulmonary DiseaseR01HL111527 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Alain T Laederach, Kevin M Weeks · 2012 to 2026
$6.6M
Pharmacological Sciences Training ProgramT32GM133352 · NIGMS · DUKE UNIVERSITY · PI Cynthia M Kuhn, David M MacAlpine · 2020 to 2026
$3.8M
Genetic dissection of oncogenic RAS-driven tumor initiation in vivoR01CA269272 · NCI · DUKE UNIVERSITY · PI CHRISTOPHER M COUNTER · 2022 to 2026
$2.2M
Variant induced RNA structure change in human genetic diseaseR35GM140844 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LAEDERACH, ALAIN T · 2021 to 2025
$2.1M
NCI NIH HHS R01 CA269272NHLBI NIH HHS R01 HL111527NIGMS NIH HHS R35 GM140844NIGMS NIH HHS T32 GM133352U.S. Department of Health & Human Services | National Institutes of Health (NIH) T32GM133352U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) R01CA269272U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) R01HL111527U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R35GM140844
6 · The paper itself

Abstract

Synonymous codons occur at unequal rates in the coding genome, with those represented least often termed 'rare.' Rare codon-enriched genes typically exhibit poor expression due to reduced transcription, mRNA stability, export, and translation. However, there are an increasing number of examples whereby rare codon-enriched genes are paradoxically highly expressed, suggestive of mechanisms to overcome the poor expression imposed by rare codons. To identify codon-dependent modifiers, we screen a targeted sgRNA library for genes that, when inactivated, increase the expression of rare versus common codon-enriched fluorescent reporters. This identifies the PAXT connection, a nuclear complex that targets transcripts to the exosome for degradation. Targeted loss of a PAXT component leads to a small but preferential increase in mRNA levels and stability and a more pronounced increase in protein expression of rare compared to common codon-enriched reporters. Transcriptomics coupled to proteomics further reveals that this leads to a preferential increase in the expression of endogenous proteins encoded by poorly expressed and long mRNAs specifically enriched in rare codons. Thus, we identify the PAXT connection as a genetic suppressor of poorly expressed genes enriched in rare codons.

Indexed as

CodonGene Expression RegulationHumansProtein BiosynthesisRNA, MessengerRNA StabilityCodonRNA, Messenger

Identifiers

PMID42897178
PMCPMC13680609

What OpenQuestion holds

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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.