Evidence map›Paper›PMID 39592233›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2025

Epitope Tagging with Genome Editing in Mice Reveals That the Proton Channel OTOP1 Is Apically Localized and Not Restricted to Type III "Sour" Taste Receptor Cells.

Joshua P Kaplan, Wenlei Ye, Heather Kileen, Ziyu Liang, Anne Tran, Jingyi Chi, Chingwen Yang, Paul Cohen, Emily R Liman

Abstract read
In one paragraph

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. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
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  5. Review
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

9 authors.

Joshua P KaplanSection of Neurobiology, Department of Biological Sciences, University of Southern California, Los Angeles, California 90089.ORCID 0000-0001-5064-2130
Wenlei YeDepartment of Physiology, University of California, San Francisco, California 94158.
Heather KileenSection of Neurobiology, Department of Biological Sciences, University of Southern California, Los Angeles, California 90089.
Ziyu LiangSection of Neurobiology, Department of Biological Sciences, University of Southern California, Los Angeles, California 90089.
Anne TranSection of Neurobiology, Department of Biological Sciences, University of Southern California, Los Angeles, California 90089.
Jingyi ChiLaboratory of Molecular Metabolism, The Rockefeller University, New York, New York 10065.ORCID 0000-0001-6013-8544
Chingwen YangCRISPR and Genome Editing Center, The Rockefeller University, New York, New York 10065.
Paul CohenLaboratory of Molecular Metabolism, The Rockefeller University, New York, New York 10065.
Emily R LimanSection of Neurobiology, Department of Biological Sciences, University of Southern California, Los Angeles, California 90089 liman@usc.edu.ORCID 0000-0003-4765-5496

Funding

Role of the proton channel OTOP1 in taste transductionR01DC013741 · NIDCD · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Sue C. Kinnamon, EMILY R. LIMAN · 2014 to 2026
$5.7M
NIDCD NIH HHS R01 DC013741
6 · The paper itself

Abstract

The gustatory system allows animals to assess the nutritive value and safety of foods prior to ingestion. The first step in gustation is the interaction of taste stimuli with one or more specific sensory receptors that are generally believed to be present on the apical surface of the taste receptor cells. However, this assertion is rarely tested. We recently identified OTOP1 as a proton channel and showed that it is required for taste response to acids (sour) and ammonium. Here, we examined the cellular and subcellular localization of OTOP1 by tagging the endogenous OTOP1 protein with an N-terminal HA epitope (HA-OTOP1). Using both male and female HA-OTOP1 mice and high-resolution imaging, we show that OTOP1 is strictly localized to the apical tips of taste cells throughout the tongue and oral cavity. Interestingly, immunoreactivity is observed in the actin-rich taste pore above the tight junctions defined by zonula occludens-1 (ZO-1) and also immediately below these junctions. Surprisingly, OTOP1 immunoreactivity is not restricted to Type III taste receptor cells (TRCs) that mediate sour taste but is also observed in glia-like Type I TRCs proposed to perform housekeeping functions, a result that is corroborated by scRNA-seq data. The apical localization of OTOP1 supports the contention that OTOP1 functions as a taste receptor and suggests that OTOP1 may be accessible to orally available compounds that could act as taste modifiers.

Indexed as

EpitopesGene EditingIon ChannelsTasteTaste BudsAnimalsCalcium ChannelsFemaleMaleMembrane ProteinsMiceMice, Inbred C57BLReceptors, Cell SurfaceTongueCalcium ChannelsEpitopesIon ChannelsMembrane ProteinsPkd2l1 protein, mouseReceptors, Cell Surfaceepitope taggingOTOP1otopetrinproton channelsensorytaste

Identifiers

PMID39592233
PMCPMC11800744

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.