Cargando…
SUMOylated Senataxin functions in genome stability, RNA degradation, and stress granule disassembly, and is linked with inherited ataxia and motor neuron disease
BACKGROUND: Senataxin (SETX) is a DNA/RNA helicase critical for neuron survival. SETX mutations underlie two inherited neurodegenerative diseases: Ataxia with Oculomotor Apraxia type 2 (AOA2) and Amyotrophic Lateral Sclerosis type 4 (ALS4). METHODS: This review examines SETX key cellular processes a...
Autores principales: | Bennett, Craig L., La Spada, Albert R. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8683630/ https://www.ncbi.nlm.nih.gov/pubmed/34263556 http://dx.doi.org/10.1002/mgg3.1745 |
Ejemplares similares
-
Tight expression regulation of senataxin, linked to motor neuron disease and ataxia, is required to avert cell-cycle block and nucleolus disassembly
por: Bennett, Craig L., et al.
Publicado: (2020) -
Protein Interaction Analysis of Senataxin and the ALS4 L389S Mutant Yields Insights into Senataxin Post-Translational Modification and Uncovers Mutant-Specific Binding with a Brain Cytoplasmic RNA-Encoded Peptide
por: Bennett, Craig L., et al.
Publicado: (2013) -
Hereditary Ataxia with a Novel Mutation in the Senataxin Gene: A Case Report
por: Moghanloo, Ehsan, et al.
Publicado: (2019) -
Aberrant Splicing of the Senataxin Gene in a Patient with Ataxia with Oculomotor Apraxia Type 2
por: Fogel, Brent L., et al.
Publicado: (2009) -
Senataxin, defective in ataxia oculomotor apraxia type 2, is involved in the defense against oxidative DNA damage
por: Suraweera, Amila, et al.
Publicado: (2007)