Evidence map›Paper›PMID 36167070›Full record

ArticleCell2022

ER stress transforms random olfactory receptor choice into axon targeting precision.

Hani J Shayya, Jerome K Kahiapo, Rachel Duffié, Katherine S Lehmann, Lisa Bashkirova, Kevin Monahan, Ryan P Dalton, Joanna Gao, Song Jiao, Ira Schieren and 2 more

Open access · greenAbstract read
In one paragraph

Article in Cell, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
6.2field-weighted citation impact, top 2% of its field
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

31 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
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  5. Cnpy1 is a candidate endoplasmic reticulum chaperone of vomeronasal type 2 GPCRs.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  10. Identifying Key Regulators in Odorant Receptor Trafficking.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 6 institutions in 1 country.

Hani J ShayyaMortimer B. Zuckerman Mind, Brain and Behavior Institute, Columbia University, New York, NY 10027, USA; Medical Scientist Training Program, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA; Integrated Program in Cellular, Molecular, and Biomedical Studies, Columbia University Irving Medical Center, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA.
Jerome K KahiapoMortimer B. Zuckerman Mind, Brain and Behavior Institute, Columbia University, New York, NY 10027, USA; Integrated Program in Cellular, Molecular, and Biomedical Studies, Columbia University Irving Medical Center, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA.
Rachel DuffiéMortimer B. Zuckerman Mind, Brain and Behavior Institute, Columbia University, New York, NY 10027, USA.
Katherine S LehmannDevelopmental Neural Plasticity Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.
Lisa BashkirovaMortimer B. Zuckerman Mind, Brain and Behavior Institute, Columbia University, New York, NY 10027, USA.
Kevin MonahanMortimer B. Zuckerman Mind, Brain and Behavior Institute, Columbia University, New York, NY 10027, USA.
Ryan P DaltonThe Miller Institute for Basic Research in Science, University of California, Berkeley, Berkeley, CA 94720, USA.
Joanna GaoBarnard College, New York, NY 10025, USA.
Song JiaoDevelopmental Neural Plasticity Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.
Ira SchierenMortimer B. Zuckerman Mind, Brain and Behavior Institute, Columbia University, New York, NY 10027, USA.
Leonardo BelluscioDevelopmental Neural Plasticity Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.
Stavros LomvardasMortimer B. Zuckerman Mind, Brain and Behavior Institute, Columbia University, New York, NY 10027, USA; Department of Biochemistry and Molecular Biophysics, Columbia University Irving Medical Center, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA; Department of Neuroscience, Columbia University Irving Medical Center, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA. Electronic address: sl682@cumc.columbia.edu.
MIND Research Institute · USNational Institutes of Health · USColumbia University · USBarnard College · USColumbia University Irving Medical Center · USMiller College · US

Funding

ER stress as the cause for dementia-associated olfactory dysfunctionR01DC015451 · NIDCD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Stavros Lomvardas · 2016 to 2026
$5.0M
Translational control of sensory identityR21DC017823 · NIDCD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI DUFFIE, RACHEL · 2019 to 2021
$486k
The unfolded protein response as a mechanism for cellular identity in the developing olfactory systemF30DC019263 · NIDCD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SHAYYA, HANI JOHN · 2020 to 2023
$191k
NIDCD NIH HHS F30 DC019263NIDCD NIH HHS R01 DC015451NIDCD NIH HHS R21 DC017823
6 · The paper itself

Abstract

Olfactory sensory neurons (OSNs) convert the stochastic choice of one of >1,000 olfactory receptor (OR) genes into precise and stereotyped axon targeting of OR-specific glomeruli in the olfactory bulb. Here, we show that the PERK arm of the unfolded protein response (UPR) regulates both the glomerular coalescence of like axons and the specificity of their projections. Subtle differences in OR protein sequences lead to distinct patterns of endoplasmic reticulum (ER) stress during OSN development, converting OR identity into distinct gene expression signatures. We identify the transcription factor Ddit3 as a key effector of PERK signaling that maps OR-dependent ER stress patterns to the transcriptional regulation of axon guidance and cell-adhesion genes, instructing targeting precision. Our results extend the known functions of the UPR from a quality-control pathway that protects cells from misfolded proteins to a sensor of cellular identity that interprets physiological states to direct axon wiring.

Indexed as

Endoplasmic Reticulum StressReceptors, OdorantAnimalsAxonsMiceOlfactory BulbOlfactory Receptor NeuronsTranscription FactorsReceptors, OdorantTranscription Factorsaxon guidanceaxon targetingcell adhesionDdit3extracellular barcodesolfactory receptorsPERKstochastic gene choicetranscriptional networksunfolded protein response

Identifiers

PMID36167070
PMCPMC9588687
OpenAlexW4297143351

What OpenQuestion holds

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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.