Rare Daily Staff
Researchers at Massachusetts General Hospital have discovered a gene that can become mutated and cause a rare balance disorder also regulates the behavior of an enzyme that increases the risk for Alzheimer’s disease.
The study, published in the journal Cell, serves as an example of how the study of a rare disease can elucidate more common ailments.
In 2008, neuroscientist Rudolph Tanzi, director of the genetics and aging research unit and co-director of the McCance Center for Brain Health at Mass General (MGM) and his colleagues identified several genes that are closely associated with Alzheimer’s, including ATXN1, which carries the genetic code for producing a protein called ataxin-1.
At the time, it was already known that a variation known as a “gain of function” mutation in ATXN1 causes a rare condition called spinocerebellar ataxia type 1 (SCA1), which leads to loss of coordination and balance, among other symptoms, including cognitive problems such as learning and memory difficulties.
However, the ATXN1 mutation that causes SCA1 is not associated with Alzheimer’s, and the role ataxin-1 might play in the disease remained unknown. “So, the big question facing us was, how does a gene involved in a balance disorder somehow increases the risk for Alzheimer’s disease?” said Tanzi, senior author of Cell paper.
The answer to that question was eventually answered by posing another. “We asked whether loss of ataxin-1 function could lead to Alzheimer’s disease,” said MGH neuroscientist Jaehong Suh. Suh supervised a team that crossbred mice that were specially bred to have the ATXN1 gene deleted, causing them to lack ataxin-1, with a second group of mice that had been bred to have Alzheimer’s disease (AD). These pairings produced offspring that were missing ataxin-1, which in turn caused their levels of an enzyme called beta-secretase 1 (BACE1) to rise dramatically.
BACE1 plays an essential role in the formation of amyloid plaques, which are clusters of damaged nerve cells and other proteins in the brain that are one of the hallmarks of Alzheimer’s. Mice lacking ataxin-1 had significantly greater deposits of amyloid plaque than the AD mice. They also had higher levels of inflamed brain tissue, formed fewer new neurons in regions associated with memory and learning, and had impaired axons, which are fibers that carry signals between neurons.
“The idea that the same protein will cause one neurodegenerative disease in a ‘gain’ situation, and cause vulnerability to another neurodegenerative disease in a ‘loss’ situation, is fascinating,” says neurogeneticist Huda Zoghbi, a professor at Baylor College of Medicine, director of the Jan and Dan Duncan Neurological Research Institute in Houston, and a coauthor of the Cell study.
Several experimental drugs that block BACE1 have failed due to toxicity but discovering ataxin-1’s role in regulating this enzyme “could provide a new avenue to safely stop formation of amyloid plaques and potentially prevent this disease before it causes symptoms,” says Tanzi.
Photo: Rudolph Tanzi, director of the genetics and aging research unit and co-director of the McCance Center for Brain Health at Mass General