Key result
Myosin XVA (MYO15A) plays an important role in stereocilia development and maintenance, and its mutations are responsible for DFNB3 and shaker-2 hearing loss in humans and mice.
Why the study?
The important roles of myosin XVA in stereocilia development and maintenance, and its mutations associated with hearing loss, require review to better appreciate and understand its mechanisms.
MYO15A plays a critical role in the development and maintenance of stereocilia, and its mutations are responsible for specific forms of hearing loss in humans and mice.
Myosins comprise a large superfamily of adenosine triphosphatases (ATPases) that interact with actin filaments to generate motility or force. Unconventional myosins are implicated in diverse cellular processes including organelle trafficking, F-actin organization and cell movement. The unconventional myosin, myosin XVA (MYO15A), is localized at the tips of stereocilia in the inner ear hair cells and plays important roles in the development and maintenance of stereocilia. Mutations in MYO15A / Myo15a genes are responsible for hearing loss DFNB3 and shaker-2 in human and mice, respectively. In the present review, we will discuss the expression and alternative splicing of the MYO15A gene, the biochemical properties of the MYO15A protein and the association of MYO15A mutations with hearing loss. We will also discuss the recent investigations into the mechanism of how MYO15A regulates stereocilia development and maintenance. At present we are just beginning to appreciate the important roles of MYO15A in stereocilia, and further investigations are warranted to fully understand them.
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Du et al. (2020) conducted a review in Hearing loss. MYO15A mutations was evaluated. Myosin XVA (MYO15A) plays an important role in stereocilia development and maintenance, and its mutations are responsible for DFNB3 and shaker-2 hearing loss in humans and mice.
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