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

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.

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Publication Details

Journal
Nature Communications
Published
2025-01-22
DOI
https://doi.org/10.1038/s41467-025-55898-8
Citations
8
Primary Topic
Hearing, Cochlea, Tinnitus, Genetics
Type
article
Field-Weighted Citation Impact
10.25

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article

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

Stacey M. Cole, Michael R. Bowl, Jesse C. Werth, Thomas B. Friedman et al.
8 citations
Nature Communications
Hearing, Cochlea, Tinnitus, Genetics
10.25
article

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

Stacey M. Cole, Michael R. Bowl, Jesse C. Werth, Thomas B. Friedman, Andrew Parker, Zane G. Moreland, Yasuharu Takagi, Melanie Barzik, Susan Morse, Carlos Aguilar, James R. Sellers, Rui Gong, Gregory M. Alushin, Arik Shams, James B. Heidings, Randall J. Harley, Daniel C. Sutton, Jonathan E. Bird, Christian Faaborg‐Andersen, Fangfang Jiang, Elizabeth Wilson, Jinho Park, Steve D. M. Brown, Ghazaleh Behnammanesh
article en
8 citations

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.

Nature CommunicationsVol. 16(1)
National Institutes of Health (US), University of Florida (US), Mary Lyon Centre at MRC Harwell (GB), National Heart, Lung, and Blood Institute (US), The London College (GB), National Institute on Deafness and Other Communication Disorders (US), University College London (GB), Rockefeller University (US)
National Institutes of Health, Medical Research Council, National Heart, Lung, and Blood Institute, National Institute on Deafness and Other Communication Disorders
Openalex Percentile: Top 2%
Hearing, Cochlea, Tinnitus, Genetics
10.25
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