This article has been reviewed according to Science X's editorial process and policies. Editors have highlighted the following attributes while ensuring the content's credibility:


peer-reviewed publication


Research team makes important step toward a therapy for a rare genetic disease

Toward a therapy for a rare genetic disease
Myo15-Cre conditional knockout mice show delayed functional and morphological cochlear pathology. Credit: Nature Communications (2023). DOI: 10.1038/s41467-023-38038-y

Usher Syndrome type 1F is a rare but severe genetic disease that causes deafness, lack of balance, and progressive blindness.

Now, a team led by researchers at Harvard Medical School, Massachusetts Eye and Ear, and The Ohio State University has made an important first step toward developing a for the disease.

The research, conducted in mice, is described Apr. 26 in Nature Communications.

The scientists designed a "mini-gene"—a shortened version of a gene—to replace the gene that is mutated in Usher 1F. The mutation renders inside the inner ear incapable of producing a involved in sound transmission. In mice, the mini-gene increased production of the missing protein, enabling the hair cells to sense sound and restoring hearing.

Because in Usher 1F involves a slightly different form of the same protein, the researchers say the same approach may be useful for preventing .

"Patients with Usher 1F are born with profound hearing loss and progressive vision loss, and so far we have been able to offer very few solutions to these families," said co-senior author Artur Indzhykulian, HMS assistant professor of otolaryngology–head and neck surgery at Mass Eye and Ear.

The researchers plan to continue testing the mini-gene in other animal models, and eventually, hope to test it in humans.

"It's completely devastating to be born deaf and then lose your vision, so we hope that this mini-gene can eventually be turned into a treatment for this disease," said co-senior author David Corey, the Bertarelli Professor of Translational Medical Science in the Blavatnik Institute at HMS.

Applying expertise to a new problem

Children with Usher Syndrome are typically born completely deaf or with severely impaired hearing, lack balance, and lose vision over time as the retina deteriorates. Blindness commonly occurs by adulthood.

These problems arise due to a mutation that interferes with production of a protein called protocadherin-15, which has slightly different forms in the ear and eye and is needed for cells in the auditory and visual systems to function properly.

Researchers in the Corey lab have long been interested in protocadherin-15's role in the inner ear. Specifically, they've wanted to know how the protein helps sensory receptors called hair cells in the ear convert vibrations from the environment into electrical signals, which the brain interprets as sound.

Corey's team previously figured out how protocadherin-15 partners with another protein, cadherin 23, in hair cells to create filaments that physically pull open ion channels as the bundles vibrate, allowing electrical current to enter the cells. In the absence of this protein, electrical current can't enter hair cells, the conversion from vibration to electricity doesn't occur, and the brain cannot detect sound.

Through this work, Corey became interested in designing a gene therapy for Usher 1F. The therapy would introduce DNA that codes for protocadherin-15 into a cell, enabling the cell to begin making the protein.

However, because protocadherin-15 is so big, its DNA is too large for the typical viral capsule used to transport genetic material into a cell. So the researchers decided to explore another option: shortening the DNA to create a mini-gene that still codes for functional protein yet is small enough to fit inside the viral capsule.

A gene becomes a mini-gene

The first step involved painstakingly mapping all 25,000 atoms in the external structure of inner-ear protocadherin-15—a process carried out by co-senior author Marcos Sotomayor, former research fellow at HMS and now associate professor of chemistry and biochemistry at The Ohio State.

Using a combination of X-ray crystallography and cryo-electron microscopy, Sotomayor found that the protein is composed of atoms arranged into what looks like 11 links in a chain.

Sotomayor made eight different versions of protocadherin-15, each with different links missing to make the protein smaller. The researchers then reverse engineered the truncated protein structures into DNA blueprints that they could test as mini-genes.

"The knowledge we gained by studying the structure of protocadherin-15 in excruciating detail allowed us to more quickly design shorter versions of the protein for gene therapy," Sotomayor explained.

Indzhykulian tested the eight mini-genes on inner ear cells in a dish. He confirmed that truncated versions of protocadherin-15 made from mini-gene DNA did bind to cadherin 23, its protein partner in hair cells.

From there, the researchers selected the three mini-genes that were small enough to fit inside the viral capsule.

Lead author Maryna Ivanchenko, instructor in neurobiology at HMS, extensively tested the three mini-genes in the ears of mice that were genetically modified to stop producing protocadherin-15. Ultimately, only one mini-gene worked.

The gene successfully prompted hair cells to make a mini version of protocadherin-15, which bound to cadherin-23 and formed the filaments needed to open ion channels. The hair cells successfully converted vibrations into electrical signals.

Auditory testing of mice that received the mini-gene showed their brains could receive the sound signal coming from their ears—the previously deaf animals could hear.

"We were all pleasantly surprised," Corey said. "We thought it would take years of optimizing and trying things and tweaking the protein structure, but this one version pretty much worked."

"The results were thrilling for us," Ivanchenko added. "The most exciting aspect of our findings was that mice that had been completely deaf could now hear almost as well as normal mice."

From the ear to the eye

While the mini-gene successfully treated in the mouse model of Usher 1F, the researchers are even more interested in its potential for treating blindness associated with the syndrome.

Since children with Usher 1F are born profoundly deaf and may lack hair cells in their inner ear, it's unlikely that the mini-gene could improve their hearing, the authors said. Additionally, many of these children are able to receive cochlear implants that allow them to hear.

Blindness is a different story, the researchers noted, because children with Usher 1F are born with normal vision. If the mini-gene could produce the form of protocadherin-15 missing in the retina, it could halt vision loss, they said.

Why start by testing the mini-gene in the mouse inner ear if treating vision loss is the main goal?

Mainly for logistical reasons, the researchers said. Lack of protocadherin-15 causes only mild vision loss in mice and progresses slowly. This means it would take years to test the mini- in mouse models, and it would be hard to tell how well they worked. By contrast, the mice were born profoundly deaf, so the researchers got clear results within a couple of weeks.

"The whole project was designed to study the ear with the idea that something that works in the ear can later be applied to the eye, as an article of faith," Corey said. "While the best test system is the mouse inner ear, the immediate goal is a treatment for blindness."

The Corey lab is now testing the mini-gene in zebrafish eyes—a better model because these fish experience more severe and rapid vision loss than mice when protocadherin-15 isn't produced in the retina.

If the mini-gene works in the zebrafish retina, the researchers will move to testing the approach in primates and, eventually, in humans.

More information: Maryna V. Ivanchenko et al, Mini-PCDH15 gene therapy rescues hearing in a mouse model of Usher syndrome type 1F, Nature Communications (2023). DOI: 10.1038/s41467-023-38038-y

Journal information: Nature Communications

Provided by Harvard Medical School
Citation: Research team makes important step toward a therapy for a rare genetic disease (2023, April 26) retrieved 22 September 2023 from
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.

Explore further

Lab grown 'mini eyes' unlock understanding of blindness in rare genetic condition


Feedback to editors