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miR-19, miR-101, and miR-130 co-regulate ATXN1 levels to potentially modulate SCA1 pathogenesis
- Publication Year :
- 2008
-
Abstract
- Spinocerebellar ataxia type 1 is caused by expansion of a translated CAG repeat in ataxin1 (ATXN1). The level of the polyglutamine-expanded protein is one of the factors that contributes to disease severity. Here we found that miR-19, miR-101 and miR-130 co-regulate ataxin1 levels and that their inhibition enhanced the cytotoxicity of polyglutamine-expanded ATXN1 in human cells. We provide a new candidate mechanism for modulating the pathogenesis of neurodegenerative diseases sensitive to protein dosage.
- Subjects :
- Spinocerebellar Ataxia Type 1
congenital, hereditary, and neonatal diseases and abnormalities
Time Factors
Glutamine
Phenylalanine
Green Fluorescent Proteins
Ataxin 1
Mice, Transgenic
Nerve Tissue Proteins
Biology
Transfection
Article
Pathogenesis
Mice
Purkinje Cells
Cerebellum
microRNA
medicine
Animals
Humans
Spinocerebellar Ataxias
Nuclear protein
RNA, Small Interfering
Ataxin-1
Cell Line, Transformed
Regulation of gene expression
General Neuroscience
Nuclear Proteins
medicine.disease
Molecular biology
Disease Models, Animal
MicroRNAs
Ataxins
Gene Expression Regulation
Spinocerebellar ataxia
Cancer research
biology.protein
Trinucleotide repeat expansion
Trinucleotide Repeat Expansion
Neuroscience
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....97acaaab8bdbb75f69c33df52fadb7d7