Evidence map›Paper›PMID 26754646›Full record

ArticleThe Journal of cell biology2016

Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth.

Andrea Lelli, Vincent Michel, Jacques Boutet de Monvel, Matteo Cortese, Montserrat Bosch-Grau, Asadollah Aghaie, Isabelle Perfettini, Typhaine Dupont, Paul Avan, Aziz El-Amraoui and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

45 citing papers in PubMed, 72 citations in OpenAlex.

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  14. Regulation of organelle size and organization during development.Seminars in cell & developmental biology · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 1 country.

Andrea LelliUnité de Génétique et Physiologie de l'Audition, Institut Pasteur, 75724 Paris, Cedex 15, France Unité Mixte de Recherche UMRS1120, Institut National de la Santé et de la Recherche Médicale, 75015 Paris, France Sorbonne Universités, Université Pierre et Marie Curie (UPMC Paris VI), Complexité du Vivant, 75005 Paris, France.
Vincent MichelUnité de Génétique et Physiologie de l'Audition, Institut Pasteur, 75724 Paris, Cedex 15, France Unité Mixte de Recherche UMRS1120, Institut National de la Santé et de la Recherche Médicale, 75015 Paris, France Sorbonne Universités, Université Pierre et Marie Curie (UPMC Paris VI), Complexité du Vivant, 75005 Paris, France.
Jacques Boutet de MonvelUnité de Génétique et Physiologie de l'Audition, Institut Pasteur, 75724 Paris, Cedex 15, France Unité Mixte de Recherche UMRS1120, Institut National de la Santé et de la Recherche Médicale, 75015 Paris, France Sorbonne Universités, Université Pierre et Marie Curie (UPMC Paris VI), Complexité du Vivant, 75005 Paris, France.
Matteo CorteseUnité de Génétique et Physiologie de l'Audition, Institut Pasteur, 75724 Paris, Cedex 15, France Unité Mixte de Recherche UMRS1120, Institut National de la Santé et de la Recherche Médicale, 75015 Paris, France Sorbonne Universités, Université Pierre et Marie Curie (UPMC Paris VI), Complexité du Vivant, 75005 Paris, France.
Montserrat Bosch-GrauUnité de Génétique et Physiologie de l'Audition, Institut Pasteur, 75724 Paris, Cedex 15, France Unité Mixte de Recherche UMRS1120, Institut National de la Santé et de la Recherche Médicale, 75015 Paris, France Sorbonne Universités, Université Pierre et Marie Curie (UPMC Paris VI), Complexité du Vivant, 75005 Paris, France.
Asadollah AghaieUnité de Génétique et Physiologie de l'Audition, Institut Pasteur, 75724 Paris, Cedex 15, France Unité Mixte de Recherche UMRS1120, Institut National de la Santé et de la Recherche Médicale, 75015 Paris, France Sorbonne Universités, Université Pierre et Marie Curie (UPMC Paris VI), Complexité du Vivant, 75005 Paris, France Syndrome de Usher et Autres Atteintes Rétino-Cochléaires, Institut de la Vision, 75012 Paris, France.
Isabelle PerfettiniUnité de Génétique et Physiologie de l'Audition, Institut Pasteur, 75724 Paris, Cedex 15, France Unité Mixte de Recherche UMRS1120, Institut National de la Santé et de la Recherche Médicale, 75015 Paris, France Sorbonne Universités, Université Pierre et Marie Curie (UPMC Paris VI), Complexité du Vivant, 75005 Paris, France.
Typhaine DupontUnité de Génétique et Physiologie de l'Audition, Institut Pasteur, 75724 Paris, Cedex 15, France Unité Mixte de Recherche UMRS1120, Institut National de la Santé et de la Recherche Médicale, 75015 Paris, France Sorbonne Universités, Université Pierre et Marie Curie (UPMC Paris VI), Complexité du Vivant, 75005 Paris, France.
Paul AvanLaboratoire de Biophysique Sensorielle, Faculté de Médecine, Université d'Auvergne; Biophysique Médicale, Centre Jean Perrin, 63000 Clermont-Ferrand, France.
Aziz El-AmraouiUnité de Génétique et Physiologie de l'Audition, Institut Pasteur, 75724 Paris, Cedex 15, France Unité Mixte de Recherche UMRS1120, Institut National de la Santé et de la Recherche Médicale, 75015 Paris, France Sorbonne Universités, Université Pierre et Marie Curie (UPMC Paris VI), Complexité du Vivant, 75005 Paris, France christine.petit@pasteur.fr aziz.el-amraoui@pasteur.fr.
Christine PetitUnité de Génétique et Physiologie de l'Audition, Institut Pasteur, 75724 Paris, Cedex 15, France Unité Mixte de Recherche UMRS1120, Institut National de la Santé et de la Recherche Médicale, 75015 Paris, France Sorbonne Universités, Université Pierre et Marie Curie (UPMC Paris VI), Complexité du Vivant, 75005 Paris, France Syndrome de Usher et Autres Atteintes Rétino-Cochléaires, Institut de la Vision, 75012 Paris, France Collège de France, 75005 Paris, France christine.petit@pasteur.fr aziz.el-amraoui@pasteur.fr.
Sorbonne Université · FRInstitut Pasteur · FRCentre Jean Perrin · FRCollège de France · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The precise architecture of hair bundles, the arrays of mechanosensitive microvilli-like stereocilia crowning the auditory hair cells, is essential to hearing. Myosin IIIa, defective in the late-onset deafness form DFNB30, has been proposed to transport espin-1 to the tips of stereocilia, thereby promoting their elongation. We show that Myo3a(-/-)Myo3b(-/-) mice lacking myosin IIIa and myosin IIIb are profoundly deaf, whereas Myo3a-cKO Myo3b(-/-) mice lacking myosin IIIb and losing myosin IIIa postnatally have normal hearing. Myo3a(-/-)Myo3b(-/-) cochlear hair bundles display robust mechanoelectrical transduction currents with normal kinetics but show severe embryonic abnormalities whose features rapidly change. These include abnormally tall and numerous microvilli or stereocilia, ungraded stereocilia bundles, and bundle rounding and closure. Surprisingly, espin-1 is properly targeted to Myo3a(-/-)Myo3b(-/-) stereocilia tips. Our results uncover the critical role that class III myosins play redundantly in hair-bundle morphogenesis; they unexpectedly limit the elongation of stereocilia and of subsequently regressing microvilli, thus contributing to the early hair bundle shaping.

Indexed as

Amino Acid SequenceAnimalsBody PatterningDeafnessHair Cells, AuditoryHEK293 CellsHumansMembrane ProteinsMiceMice, KnockoutMice, Mutant StrainsMicrofilament ProteinsMicrovilliMolecular Sequence DataMyosin Heavy ChainsMyosin Type IIIespin protein, mouseMembrane ProteinsMicrofilament ProteinsMORN4 protein, mouseMYO3A protein, mouseMYO3B protein, mouseMyosin Heavy ChainsMyosin Type III

Identifiers

PMID26754646
PMCPMC4738386
OpenAlexW2279794797

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.