Evidence map›Paper›PMID 40668674›Full record

ArticleCell reports2025

Mex3a-dependent post-transcriptional silencing ensures olfactory receptor diversity and axon guidance specificity.

Rachel Duffié, Hani Shayya, Martín Escamilla Del Arenal, Miao Wang, Jerome Kahiapo, Aileen Ugurbil, Abdurrahman Keskin, Fiona Clowney, Elizaveta V Bashkirova, Ariel D Pourmorady and 7 more

Abstract read
In one paragraph

Article in Cell reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

17 authors.

Rachel DuffiéMortimer B. Zuckerman Mind, Brain, and Behavior Institute, Columbia University, New York, NY 10027, USA.
Hani ShayyaMortimer B. Zuckerman Mind, Brain, and Behavior Institute, Columbia University, New York, NY 10027, USA.
Martín Escamilla Del ArenalMortimer B. Zuckerman Mind, Brain, and Behavior Institute, Columbia University, New York, NY 10027, USA.
Miao WangMortimer B. Zuckerman Mind, Brain, and Behavior Institute, Columbia University, New York, NY 10027, USA.
Jerome KahiapoMortimer B. Zuckerman Mind, Brain, and Behavior Institute, Columbia University, New York, NY 10027, USA.
Aileen UgurbilMortimer B. Zuckerman Mind, Brain, and Behavior Institute, Columbia University, New York, NY 10027, USA.
Abdurrahman KeskinDepartment of Biological Sciences, Columbia University, New York, NY 10027, USA.
Fiona ClowneyMortimer B. Zuckerman Mind, Brain, and Behavior Institute, Columbia University, New York, NY 10027, USA.
Elizaveta V BashkirovaMortimer B. Zuckerman Mind, Brain, and Behavior Institute, Columbia University, New York, NY 10027, USA.
Ariel D PourmoradyMortimer B. Zuckerman Mind, Brain, and Behavior Institute, Columbia University, New York, NY 10027, USA.
Ira SchierenMortimer B. Zuckerman Mind, Brain, and Behavior Institute, Columbia University, New York, NY 10027, USA.
Humberto Ibarra AvilaMortimer B. Zuckerman Mind, Brain, and Behavior Institute, Columbia University, New York, NY 10027, USA.
Luke E BerchowitzDepartment of Genetics and Development, Columbia University, Vagelos College of Physicians and Surgeons, New York, NY 10032, USA.
Francisco M BarrigaSystems Oncology Program, Vall d'Hebron Institute of Oncology (VHIO), Vall d'Hebron Barcelona Hospital Campus, 08035 Barcelona, Spain; Institute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology (BIST), Baldiri i Reixac 10, 08028 Barcelona, Spain.
Eduard BatlleInstitute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology (BIST), Baldiri i Reixac 10, 08028 Barcelona, Spain; Centro de Investigación Biomédica en Red de Cáncer (CIBERONC), Barcelona, Spain; Institució Catalana de Recerca i Estudis Avançats (ICREA), Barcelona, Spain.
Marko JovanovicDepartment of Biological Sciences, Columbia University, New York, NY 10027, USA.
Stavros LomvardasMortimer B. Zuckerman Mind, Brain, and Behavior Institute, Columbia University, New York, NY 10027, USA; Kavli Institute for Brain Sciences at Columbia University, New York, NY 10027, USA; Department of Biochemistry and Molecular Biophysics, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA. Electronic address: sl682@cumc.columbia.edu.

Funding

Olfactory receptor mRNAs as lncRNAs that regulate genomic interactionsR01DC018744 · NIDCD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Stavros Lomvardas · 2020 to 2026
$3.7M
How dynamic molecular interactions of RNA Binding Proteins drive post-transcriptional gene expression changesR35GM152258 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Marko Jovanovic · 2024 to 2026
$1.6M
BD Biosciences InfluxS10OD020056 · OD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SNOECK, HANS-WILLEM E · 2015 to 2015
$600k
Translational control of sensory identityR21DC017823 · NIDCD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI DUFFIE, RACHEL · 2019 to 2021
$486k
Five-laser Aurora spectral flow cytometerS10OD030282 · OD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CREUSOT, REMI J · 2022 to 2022
$361k
NIDCD NIH HHS R01 DC018744NIDCD NIH HHS R21 DC017823NIGMS NIH HHS R35 GM152258NIH HHS S10 OD020056NIH HHS S10 OD030282
6 · The paper itself

Abstract

Olfactory sensory neurons (OSNs) use olfactory receptor (OR)-specific patterns of endoplasmic reticulum (ER) stress to transform OR sequence identity into axon guidance precision. However, during neuronal differentiation, OSNs transiently co-express random combinations of OR genes, which could generate unpredictable ER stress signatures that could lead to axon miswiring. Here, we show that post-transcriptional OR silencing by the transiently expressed and cytoplasmic RING and KH domain protein Mex3a, decouples OR transcription from OR protein-induced ER stress, until the onset of singular OR transcription. Consequently, conditional Mex3a deletion results in premature ER stress during the polygenic stage of OR transcription, which biases OR choice toward the OR alleles that are transcribed first and perturbs the specificity of OR-regulated axon targeting, disrupting the glomerular map of odor representation in the olfactory bulb. Our experiments reveal the critical role of post-transcriptional gene regulation in a fundamental cellular pathway that influences the assembly of neuronal circuits.

Indexed as

Axon GuidanceAxonsGene SilencingOlfactory Receptor NeuronsReceptors, OdorantRNA-Binding ProteinsAnimalsEndoplasmic Reticulum StressMiceOlfactory BulbReceptors, OdorantRNA-Binding Proteinsaxon guidanceCP: NeuroscienceER stressmRNA translationRNA degradation

Identifiers

PMID40668674
PMCPMC12517755

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.