A spatial code governs olfactory receptor choice and aligns sensory maps in the nose and brain
Summary
bioRxiv. 2025 May 08:2025.05.02.651738. doi: 10.1101/2025.05.02.651738. Although topographical maps organize many peripheral sensory systems, mouse olfactory sensory neurons (OSNs) are thought to randomly choose which one of ∼1,100 possible olfactory receptors (ORs) to express, with spatial organization in the olfactory epithelium limited to a handful of broad anatomical "zones" that modestly restrict OR choice. Here, we reveal that each OR is instead expressed at a unique mean dorsoventral
Content
# A spatial code governs olfactory receptor choice and aligns sensory maps in the nose and brain
*Published: 2026 Apr 28*
bioRxiv. 2025 May 08:2025.05.02.651738. doi: 10.1101/2025.05.02.651738.
Although topographical maps organize many peripheral sensory systems, mouse
olfactory sensory neurons (OSNs) are thought to randomly choose which one of
∼1,100 possible olfactory receptors (ORs) to express, with spatial organization
in the olfactory epithelium limited to a handful of broad anatomical "zones"
that modestly restrict OR choice. Here, we reveal that each OR is instead
expressed at a unique mean dorsoventral position, thereby instantiating a
stereotyped receptor map in the olfactory epithelium. OSN dorsoventral
identities are encoded by a coherent gene expression program, which includes key
transcription factors and axon guidance molecules; use of this program reflects
a dorsoventral gradient in retinoic acid signaling, translates each physical
location into a spatially appropriate distribution of potential OR choices, and
aligns receptor maps in the nose and brain. Spatial order in the olfactory
system, therefore, arises from a continuously varying transcriptional code that
precisely organizes the many discrete channels responsible for smell.
DOI: 10.1016/j.cell.2026.03.051