Ataxin 1
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Ataxin-1 is a protein that in humans is encoded by the ATXN1 gene.[1][2]
Mutations in this gene have been linked to neuronal death in suffers of spinocerebellar ataxia type 1, an inherited neurodegenerative disease characterized by a progressive loss of cerebellar neurons. Pathogenic ATXN1 contains an abnormally elongated stretch of the amino acid glutamine. This causes the protein to spontaneously misfold and form aggregates.[3] It has been shown that other neuronal proteins can modulate the formation of Ataxin-1 aggregates and that this in turn may affect aggregate-induced toxicity.[4]
Interactions
Ataxin 1 has been shown to interact with:
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References
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External links
- GeneReviews/NIH/NCBI/UW entry on Spinocerebellar Ataxia Type 1
- ataxin-1 at the US National Library of Medicine Medical Subject Headings (MeSH)
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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