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

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.

Authors

Institutions

Publication Details

Journal
Cell Reports
Published
2025-07-16
DOI
https://doi.org/10.1016/j.celrep.2025.115979
Citations
2
Primary Topic
Olfactory and Sensory Function Studies
Type
article
Field-Weighted Citation Impact
2.93

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

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

Jerome Kahiapo, Rachel Duffié, Ariel Pourmorady, Elizaveta Bashkirova et al.
2 citations
Cell Reports
Olfactory and Sensory Function Studies
2.93
article

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

Jerome Kahiapo, Rachel Duffié, Ariel Pourmorady, Elizaveta Bashkirova, Francisco M. Barriga, Hani Shayya, Ira Schieren, Abdurrahman Keskin, Marko Jovanović, Luke Edwin Berchowitz, Eduard Batlle, Stavros Lomvardas, Fiona Clowney, Miao Wang, Humberto Ibarra Avila, Martín Escamilla del Arenal, Aileen Ugurbil
article en
2 citations

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.

Cell ReportsVol. 44(8)
MIND Research Institute (US), Institute for Research in Biomedicine (ES), Columbia University (US)
National Institute on Deafness and Other Communication Disorders
Zero hunger
Openalex Percentile: Top 10%
Olfactory and Sensory Function Studies
2.93
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.