Evidence map›Paper›PMID 19934034›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2009

The transmembrane inner ear (Tmie) protein is essential for normal hearing and balance in the zebrafish.

Michelle R Gleason, Aaron Nagiel, Sophie Jamet, Maria Vologodskaia, Hernán López-Schier, A J Hudspeth

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
1.7field-weighted citation impact, top 18% of its field
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

54 citing papers in PubMed, 99 citations in OpenAlex.

  1. Article
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  5. Transmembrane Channel-Like (Tmc) Subunits Contribute to Frequency Sensitivity in the Zebrafish Utricle.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  6. Article
  7. Article
  8. The conductance and organization of the TMC1-containing mechanotransducer channel complex in auditory hair cells.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. How Zebrafish Can Drive the Future of Genetic-based Hearing and Balance Research.Journal of the Association for Research in Otolaryngology : JARO · 2021
    Review
  14. Review
  15. Review
  16. Navigating Hereditary Hearing Loss: Pathology of the Inner Ear.Frontiers in cellular neuroscience · 2021
    Review
  17. Review
  18. Article
  19. Article
  20. Disruption ofThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
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

6 authors at 3 institutions in 2 countries.

Michelle R GleasonHoward Hughes Medical Institute and Laboratory of Sensory Neuroscience, The Rockefeller University, New York, NY 10065, USA.
Aaron Nagiel
Sophie Jamet
Maria Vologodskaia
Hernán López-Schier
A J Hudspeth
Rockefeller University · USHoward Hughes Medical Institute · USBarcelona Biomedical Research Park · ES

Funding

Weill Cornell/Rockefeller/Sloan-Kettering MST ProgramT32GM007739 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI HSU, KATHARINE C · 1985 to 2023
$51.1M
TRANSDUCTION MECHANISM OF HAIR CELLSR01DC000241 · NIDCD · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI HUDSPETH, ALBERT JAMES · 1989 to 2011
$4.1M
Specificity of neuronal Connections in the Zebrafish Lateral LineF30NS062486 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI NAGIEL, AARON · 2008 to 2011
$154k
ELECTROPHYSIOLOGICAL STUDIES OF THE VOMERONASAL SYSTEMF32DC000241 · NIDCD · WORCESTER FOUNDATION FOR BIOMEDICAL RES · PI JANG, TAICHANG · 1996 to 1998
–
Howard Hughes Medical InstituteNIDCD NIH HHS DC00241NIDCD NIH HHS F32 DC000241NIDCD NIH HHS R01 DC000241NIGMS NIH HHS GM07739NIGMS NIH HHS T32 GM007739NINDS NIH HHS F30 NS062486
6 · The paper itself

Abstract

Little is known about the proteins that mediate mechanoelectrical transduction, the process by which acoustic and accelerational stimuli are transformed by hair cells of the inner ear into electrical signals. In our search for molecules involved in mechanotransduction, we discovered a line of deaf and uncoordinated zebrafish with defective hair-cell function. The hair cells of mutant larvae fail to incorporate fluorophores that normally traverse the transduction channels and their ears lack microphonic potentials in response to vibratory stimuli. Hair cells in the posterior lateral lines of mutants contain numerous lysosomes and have short, disordered hair bundles. Their stereocilia lack two components of the transduction apparatus, tip links and insertional plaques. Positional cloning revealed an early frameshift mutation in tmie, the zebrafish ortholog of the mammalian gene transmembrane inner ear. The mutant line therefore affords us an opportunity to investigate the role of the corresponding protein in mechanoelectrical transduction.

Indexed as

AnimalsDeafnessEar, InnerFrameshift MutationHair Cells, AuditoryHearingMechanotransduction, CellularMembrane ProteinsPostural BalanceZebrafishZebrafish ProteinsMembrane ProteinsTmie protein, zebrafishZebrafish Proteins

Identifiers

PMID19934034
PMCPMC2781060
OpenAlexW2009512150

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.