Evidence map›Paper›PMID 39843411›Full record

ArticleNature communications2025

Myosin-based nucleation of actin filaments contributes to stereocilia development critical for hearing.

Zane G Moreland, Fangfang Jiang, Carlos Aguilar, Melanie Barzik, Rui Gong, Ghazaleh Behnammanesh, Jinho Park, Arik Shams, Christian Faaborg-Andersen, Jesse C Werth and 14 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Modulation of Filopodial Myosin Function.bioRxiv : the preprint server for biology · 2025
    Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. 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

24 authors.

Zane G Moreland *Department of Pharmacology and Therapeutics, University of Florida, Gainesville, FL, USA.ORCID http://orcid.org/0000-0003-3582-6374
Fangfang Jiang *Department of Pharmacology and Therapeutics, University of Florida, Gainesville, FL, USA.ORCID http://orcid.org/0000-0003-4659-9322
Carlos Aguilar *Mammalian Genetics Unit, MRC Harwell Institute, Didcot, UK.ORCID http://orcid.org/0000-0002-4655-1778
Melanie Barzik *Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.ORCID http://orcid.org/0000-0003-3003-1281
Rui GongLaboratory of Structural Biophysics and Mechanobiology, The Rockefeller University, New York, NY, USA.ORCID http://orcid.org/0000-0001-7270-2974
Ghazaleh BehnammaneshDepartment of Pharmacology and Therapeutics, University of Florida, Gainesville, FL, USA.ORCID http://orcid.org/0009-0008-9342-3665
Jinho ParkDepartment of Pharmacology and Therapeutics, University of Florida, Gainesville, FL, USA.ORCID http://orcid.org/0000-0002-3664-2238
Arik ShamsLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.ORCID http://orcid.org/0000-0002-0151-0593
Christian Faaborg-AndersenLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.ORCID http://orcid.org/0000-0002-9134-4671
Jesse C WerthLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.ORCID http://orcid.org/0000-0003-0124-9273
Randall HarleyLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.ORCID http://orcid.org/0000-0002-8519-5366
Daniel C SuttonLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.
James B HeidingsDepartment of Pharmacology and Therapeutics, University of Florida, Gainesville, FL, USA.ORCID http://orcid.org/0000-0001-7358-1705
Stacey M ColeLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.
Andrew ParkerMammalian Genetics Unit, MRC Harwell Institute, Didcot, UK.
Susan MorseMammalian Genetics Unit, MRC Harwell Institute, Didcot, UK.
Elizabeth WilsonLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.
Yasuharu TakagiLaboratory of Molecular Physiology, Cell and Developmental Biology Center, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD, USA.
James R SellersLaboratory of Molecular Physiology, Cell and Developmental Biology Center, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD, USA.ORCID http://orcid.org/0000-0001-6296-564X
Steve D M BrownMammalian Genetics Unit, MRC Harwell Institute, Didcot, UK.
Thomas B FriedmanLaboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.ORCID http://orcid.org/0000-0003-4614-6630
Gregory M AlushinLaboratory of Structural Biophysics and Mechanobiology, The Rockefeller University, New York, NY, USA.ORCID http://orcid.org/0000-0001-7250-4484
Michael R BowlMammalian Genetics Unit, MRC Harwell Institute, Didcot, UK. m.bowl@ucl.ac.uk.ORCID http://orcid.org/0000-0001-7971-445X
Jonathan E BirdDepartment of Pharmacology and Therapeutics, University of Florida, Gainesville, FL, USA. j.bird@ufl.edu.ORCID http://orcid.org/0000-0001-5531-8794

Funding

Identification of Genes Causing Syndromic And Nonsyndromic Hearing ImpairmentZ01DC000039 · NIDCD · NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS · PI FRIEDMAN, THOMAS BAER · 1997 to 2008
$7.2M
Molecular Mechanisms of Hair Bundle Development and MaintenanceR01DC018827 · NIDCD · UNIVERSITY OF FLORIDA · PI Jonathan Edward Bird · 2020 to 2026
$3.0M
SPEECH AND HEARING SCIENCEST32DC000039 · NIDCD · CUNY GRADUATE SCH AND UNIV CTR · PI SCHWARTZ, RICHARD G · 1992 to 2002
$429k
Exploring the Biophysical Landscape of Tip Density Biomolecular Condensates in Mechanosensory StereociliaF31DC021881 · NIDCD · UNIVERSITY OF FLORIDA · PI MORELAND, ZANE G · 2024 to 2025
$87k
Intramural NIH HHS Z01 DC000039NIDCD NIH HHS F31 DC021881NIDCD NIH HHS R01 DC018827NIDCD NIH HHS T32 DC000039RCUK | Medical Research Council (MRC) MC_U142684175RCUK | Medical Research Council (MRC) MC_UP_1503/2RCUK | Medical Research Council (MRC) MR/X004597/1U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) HL006049U.S. Department of Health & Human Services | NIH | National Institute on Deafness and Other Communication Disorders (NIDCD) DC000039U.S. Department of Health & Human Services | NIH | National Institute on Deafness and Other Communication Disorders (NIDCD) F31DC021881U.S. Department of Health & Human Services | NIH | National Institute on Deafness and Other Communication Disorders (NIDCD) R01DC018827
6 · The paper itself

Abstract

Assembly of actin-based stereocilia is critical for cochlear hair cells to detect sound. To tune their mechanosensivity, stereocilia form bundles composed of graded rows of ascending height, necessitating the precise control of actin polymerization. Myosin 15 (MYO15A) drives hair bundle development by delivering critical proteins to growing stereocilia that regulate actin polymerization via an unknown mechanism. Here, we show that MYO15A is itself an actin nucleation-promoting factor. Moreover, a deafness-causing mutation in the MYO15A actin-binding interface inhibits nucleation activity but still preserves some movement on filaments in vitro and partial trafficking on stereocilia in vivo. Stereocilia fail to elongate correctly in this mutant mouse, providing evidence that MYO15A-driven actin nucleation contributes to hair bundle biogenesis. Our work shows that in addition to generating force and motility, the ATPase domain of MYO15A can directly regulate actin polymerization and that disrupting this activity can promote cytoskeletal disease, such as hearing loss.

Indexed as

Actin CytoskeletonHair Cells, AuditoryHearingMyosinsStereociliaActinsAnimalsDeafnessHumansMiceMutationActinsMyo15 protein, mouseMyosins

Identifiers

PMID39843411
PMCPMC11754657

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.