ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2025
Identifying Key Regulators in Odorant Receptor Trafficking.
Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
Abstract
Odor detection in mammals is primarily mediated by odorant receptors (ORs), the largest family of G-protein-coupled receptors, expressed in olfactory sensory neurons (OSNs; Buck and Axel, 1991). However, most ORs exhibit little or no cell surface expression in nonolfactory cell types (Lu et al., 2003; Hague et al., 2004). While the accessory protein RTP1 and RTP2 enhance the expression of certain ORs, we hypothesized that additional proteins coregulated with RTP1 and RTP2 during OSN maturation may further enhance OR cell surface expression (Saito et al., 2004; Zhuang and Matsunami, 2007). To test this, we developed a computational pipeline based on publicly available single-cell transcriptomic data to create an interactive tool for exploring gene expression during OSN maturation. Using this tool, we identified genes coregulated with Rtp1 during olfactory development. Three genes-Gfy, Clgn, and Syt1-exhibited transcriptional profiles similar to Rtp1. When coexpressed with an OR, these genes, in combination with Rtp1, promoted cell-surface expression of the tested ORs. Importantly, we demonstrated a physical interaction between Syt1 and an OR (Or1ad1) via co-immunoprecipitation, suggesting a novel role for Syt1 in OR trafficking or stabilization. We also observed localization of Syt1 protein in OSN cilia in both male and female mice. Together, these findings provide new insights into OSN development and the molecular mechanisms underlying OR biogenesis, paving the way for further research into the functional regulation of the olfactory systems.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.