Essential key to hearing sensitivity discovered

Essential key to hearing sensitivity discovered
Jung-Bum Shin, PhD, of UVA's Department of Neuroscience, has shed light on the biological architecture that lets us hear - and on a genetic disorder that causes both deafness and blindness. Credit: Dan Addison, UVA Communications

New research from the University of Virginia School of Medicine is shedding light on the biological architecture that lets us hear—and on a genetic disorder that causes both deafness and blindness.

Sihan Li, a graduate student in the lab of Jung-Bum Shin, Ph.D., of UVA's Department of Neuroscience, has made a surprising discovery about how the hearing organ in mammals achieves its extraordinary sensitivity.

It was long suspected that tiny molecular motors maintain the proper tension in the so-called hair cell mechanoreceptors that are located in the inner ear. This tension is a key factor in how we detect sound, similarly to how a taut fishing line indicates nibbling fish.

The research team led by Li and Shin demonstrated that maintaining this tension was the responsibility of a protein called Myosin-VIIa. They also found that there is not just one Myosin-VIIa but several—subtle variations that all play important roles. Problems with these protein "isoforms," as the variations are known, lead to hearing loss, Shin's team found. That speaks to the vital importance of these underappreciated variations in proteins.

"Our sense of hearing is incredibly sensitive, and our study identified a very important component in the underlying mechanism," Shin said. "Furthermore, we showed that the molecular machinery that enables hearing is much more complicated than we thought, with each protein having multiple sister forms that have distinct functions."

Genetic Hearing Loss

Myosin-VIIa is made by the gene MYO7A. Mutations in that gene cause a rare genetic disorder, Usher syndrome type 1. Children with the syndrome typically are born deaf and then suffer progressive vision loss. The discovery by the Shin lab will contribute towards a better understanding of this disease.

Shin and his team found that lab mice lacking proper Myosin-VIIa isoforms developed hearing loss. His work shows that the mice were able to develop hair cells, but their function was impaired and grew progressively worse. (Myosin-VIIa is also produced in the retina, the part of the eye that senses light. The Shin lab did not look at that, but his work might shed more light on how impairments in Myosin-VIIa affect vision as well.)

One of the great questions arising from the work, the researchers say, is exactly why the inner ear uses multiple isoforms of this . Finding those answers will help us understand an important aspect of our ability to hear, and it may one day help doctors develop new treatments for .

"After all, the flip side of the extreme sensitivity of our hearing organ is that it is also very vulnerable to stress factors, such as noise and age. We have found one important mechanism by which the ear achieves its sensitivity," Shin said. "This will help us understand the harmful processes that lead to the loss of our sensitivity with age or due to noise trauma, laying the foundation for the development of preventative and therapeutic strategies."

The researchers have published their findings in the scientific journal Nature Communications.

More information: Sihan Li et al, Myosin-VIIa is expressed in multiple isoforms and essential for tensioning the hair cell mechanotransduction complex, Nature Communications (2020). DOI: 10.1038/s41467-020-15936-z

Journal information: Nature Communications

Citation: Essential key to hearing sensitivity discovered (2020, May 26) retrieved 4 February 2023 from
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