A protein, called Staufen1, accumulates in cells of patients suffering from degenerative ataxia or amyotrophic lateral sclerosis (ALS), scientists at University of Utah Health report for the first time.
Depleting the protein from affected mice improved symptoms including motor function. These results suggest that targeting Staufen1 could have therapeutic potential in people.
“This is a completely new avenue for thinking about neurodegenerative diseases. A protein that had never been known to be involved in neurodegeneration is now a great target for drug treatments,"
says Stefan Pulst, M.D., chair of Neurology at U of U Health and senior researcher on the study.
Staufen1 And Ataxin2
Previously, researchers had not considered Staufen1 a culprit in neurodegenerative disease until they discovered its association with ataxia, a rare condition that causes patients to lose control of their movement. They found that Staufen1 binds Ataxin2, a protein that is both responsible for ataxia and a risk factor for ALS.
Spinocerebellar ataxia type 2 (SCA2) is a form of ataxia marked by progressive problems with movement. People with this condition initially experience problems with coordination and balance (ataxia). Other early signs and symptoms of SCA2 include speech and swallowing difficulties, rigidity, tremors, and weakness in the muscles that control eye movement (ophthalmoplegia). Eye muscle weakness leads to a decreased ability to make rapid eye movements (saccadic slowing).
In this study, the researchers found that Staufen1 levels are increased in cells from SCA2 and ALS patients as well as in SCA2 animal models.
[caption id=“attachment_97276” align=“aligncenter” width=“680”] STAU1 directly interacts with human PCP2 mRNA.
Credit: Sharan Paul, et al. CC-BY[/caption]
The role for Staufen1 in disease pathology became evident upon genetically depleting it from mice with an ataxia-like condition. The animals' condition improved at both physiological and molecular levels.
Beginning at 12 weeks of age, mice performed significantly better on a rotarod performance test, measuring the length of time the animals could walk or run on an accelerating spinning rod. In addition, the expression of a handful of proteins that had diminished in brain cells during disease reverted back to near-normal levels.
“Staufen was first discovered in the fruit fly and has been studied for 30 years, but it had never been connected to anything related to disease. This is a novel finding, “
says Pulst. Future investigations will focus on determining whether drugs or therapies that reduce Staufen1 could be developed as treatments for multiple diseases.
Stress Granule Clues
Beyond those applications, the biology of Staufen1 could reveal new clues about neurodegenerative disease.
The protein accumulates with Ataxin2 and other proteins and RNAs in dense clusters called stress granules, a hallmark of ataxia, ALS and other conditions such as frontotemporal dementia. When Staufen1 was depleted from mice with ataxia, it not only improved the pathology of disease but also rid cells of stress granules.
While the precise role of stress granules is still an intensive area of study, they are believed to help cells weather stress caused by toxins or certain disease conditions, explains co-author Daniel Scoles, Ph.D., associate professor of Neurology at U of U Health. One function could be to prevent proteins from being made under suboptimal conditions.
[caption id=“attachment_97277” align=“aligncenter” width=“680”] Silencing of STAU1 mitigates SCA2 phenotypes.
Credit: Sharan Paul, et al. CC-BY[/caption]
The findings connect Staufen1 to the emerging concept that neurodegenerative diseases are linked to malfunctions in the way cells cope with cellular stress. One implication, says Scoles, is that Staufen1-targeted therapies could work against a number of disorders in which stress granules emerge, although it remains to be determined whether the aggregates themselves lead to disease.
“Our results put the stress granule in focus as a structure to target in disease,"
The work was supported by the National Institutes of Neurological Disorders and Stroke, Noorda foundation, and the Target ALS Foundation.
Sharan Paul, Warunee Dansithong, Karla P. Figueroa, Daniel R. Scoles & Stefan M. Pulst Staufen1 links RNA stress granules and autophagy in a model of neurodegeneration Nature Communications volume 9, Article number: 3648 (2018)
Top Image: Sharan Paul, et al. CC-BY