Oct 04, 2017
Raising hope of preventing glaucoma, one of the most common causes of irreparable blindness, scientists have used the gene editing method CRISPR-Cas9 to interrupt a mutant gene that is liable for some forms of the ailment.
The study, published in the journal Proceedings of the National Academy of Sciences, involved the elimination of the mutated myocilin protein from a mouse model of human glaucoma and cultured human cells through the use of CRISPR-Cas9, which can alter DNA sequences and gene function.
Mutations in myocilin are implicated in juvenile- and adult-onset primary open-angle glaucoma.
In their experiments, researchers found that removing the mutated protein by disrupting the mutant myociln results in lowered intraocular pressure, which in turn prevents glaucomatous damage to the eye.
"As scientists we don't want to just discover a diseased gene, we want to understand what the gene does and, in this case, have a better understanding of glaucoma so that it can be more effectively treated," said senior author of the study Val Sheffield from University of Iowa in the US.
"No one knows what this gene does, except that its mutant form causes glaucoma," Sheffield said.
Glaucoma is a common vision and neurodegenerative disorder affecting three to five per cent of people over the age of 40.
An early precursor to the most common form of this disease known as primary open-angle glaucoma is high intraocular pressure - fluid pressure inside the eye - that damages retinal ganglion axons at the optic nerve and leads to death of retinal ganglion cells that carry the visual signals to the brain, which can cause blindness.
Myocilin is a protein found in the trabecular meshwork - a part of the eye that regulates intraocular pressure.
A mutation in the myocilin gene can cause high intraocular pressure.
Scientists found that genome editing using CRISPR-Cas9 to disrupt the mutant myocilin gene prevented production of the mutant protein, which prevented elevated intraocular pressure in mouse eyes, thus totally preventing this human form of glaucoma in mice.
News Source: IANS
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