Function of bidirectional sensitivity in the otolith organs established by transcription factor Emx2

The inner ear is highly organized, with distinct domains being located across the Line of Polarity Reversal (LPR). Here they show that Emx2 establishes the LPR and bidirectional selectivity of otolith organs, and that loss of the LPR in mice affects swimming and balance.

Bibliographic Details
Main Authors: Young Rae Ji, Yosuke Tona, Talah Wafa, Matthew E. Christman, Edward D. Tourney, Tao Jiang, Sho Ohta, Hui Cheng, Tracy Fitzgerald, Bernd Fritzsch, Sherri M. Jones, Kathleen E. Cullen, Doris K. Wu
Format: Article
Language:English
Published: Nature Portfolio 2022-10-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-022-33819-3
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author Young Rae Ji
Yosuke Tona
Talah Wafa
Matthew E. Christman
Edward D. Tourney
Tao Jiang
Sho Ohta
Hui Cheng
Tracy Fitzgerald
Bernd Fritzsch
Sherri M. Jones
Kathleen E. Cullen
Doris K. Wu
author_facet Young Rae Ji
Yosuke Tona
Talah Wafa
Matthew E. Christman
Edward D. Tourney
Tao Jiang
Sho Ohta
Hui Cheng
Tracy Fitzgerald
Bernd Fritzsch
Sherri M. Jones
Kathleen E. Cullen
Doris K. Wu
author_sort Young Rae Ji
collection DOAJ
description The inner ear is highly organized, with distinct domains being located across the Line of Polarity Reversal (LPR). Here they show that Emx2 establishes the LPR and bidirectional selectivity of otolith organs, and that loss of the LPR in mice affects swimming and balance.
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spelling doaj.art-5bead77669984065ab06d028bf6cb8e42022-12-22T03:53:40ZengNature PortfolioNature Communications2041-17232022-10-0113111410.1038/s41467-022-33819-3Function of bidirectional sensitivity in the otolith organs established by transcription factor Emx2Young Rae Ji0Yosuke Tona1Talah Wafa2Matthew E. Christman3Edward D. Tourney4Tao Jiang5Sho Ohta6Hui Cheng7Tracy Fitzgerald8Bernd Fritzsch9Sherri M. Jones10Kathleen E. Cullen11Doris K. Wu12Section on Sensory Cell Regeneration and Development, Laboratory of Molecular Biology, National Institute on Deafness and Other Communication Disorders, National Institutes of HealthSection on Sensory Cell Regeneration and Development, Laboratory of Molecular Biology, National Institute on Deafness and Other Communication Disorders, National Institutes of HealthMouse Auditory Testing Core Facility, National Institute on Deafness and Other Communication Disorders, National Institutes of HealthDepartment of Biomedical Engineering, Johns Hopkins University School of MedicineDepartment of Biomedical Engineering, Johns Hopkins University School of MedicineSection on Sensory Cell Regeneration and Development, Laboratory of Molecular Biology, National Institute on Deafness and Other Communication Disorders, National Institutes of HealthSection on Sensory Cell Regeneration and Development, Laboratory of Molecular Biology, National Institute on Deafness and Other Communication Disorders, National Institutes of HealthBioinformatics and Biostatistics Collaboration Core, National Institute on Deafness and Other Communication Disorders, National Institutes of HealthMouse Auditory Testing Core Facility, National Institute on Deafness and Other Communication Disorders, National Institutes of HealthDepartment of Biology & Department of Otolaryngology, University of IowaDepartment of Special Education and Communication Disorders, 301 Barkley Memorial Center, University of Nebraska-LincolnDepartment of Biomedical Engineering, Johns Hopkins University School of MedicineSection on Sensory Cell Regeneration and Development, Laboratory of Molecular Biology, National Institute on Deafness and Other Communication Disorders, National Institutes of HealthThe inner ear is highly organized, with distinct domains being located across the Line of Polarity Reversal (LPR). Here they show that Emx2 establishes the LPR and bidirectional selectivity of otolith organs, and that loss of the LPR in mice affects swimming and balance.https://doi.org/10.1038/s41467-022-33819-3
spellingShingle Young Rae Ji
Yosuke Tona
Talah Wafa
Matthew E. Christman
Edward D. Tourney
Tao Jiang
Sho Ohta
Hui Cheng
Tracy Fitzgerald
Bernd Fritzsch
Sherri M. Jones
Kathleen E. Cullen
Doris K. Wu
Function of bidirectional sensitivity in the otolith organs established by transcription factor Emx2
Nature Communications
title Function of bidirectional sensitivity in the otolith organs established by transcription factor Emx2
title_full Function of bidirectional sensitivity in the otolith organs established by transcription factor Emx2
title_fullStr Function of bidirectional sensitivity in the otolith organs established by transcription factor Emx2
title_full_unstemmed Function of bidirectional sensitivity in the otolith organs established by transcription factor Emx2
title_short Function of bidirectional sensitivity in the otolith organs established by transcription factor Emx2
title_sort function of bidirectional sensitivity in the otolith organs established by transcription factor emx2
url https://doi.org/10.1038/s41467-022-33819-3
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