Cargando…
ALS/FTD-associated protein FUS induces mitochondrial dysfunction by preferentially sequestering respiratory chain complex mRNAs
Dysregulation of the DNA/RNA-binding protein FUS causes certain subtypes of ALS/FTD by largely unknown mechanisms. Recent evidence has shown that FUS toxic gain of function due either to mutations or to increased expression can disrupt critical cellular processes, including mitochondrial functions....
Autores principales: | Tsai, Yueh-Lin, Coady, Tristan H., Lu, Lei, Zheng, Dinghai, Alland, Isabel, Tian, Bin, Shneider, Neil A., Manley, James L. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7263147/ https://www.ncbi.nlm.nih.gov/pubmed/32381627 http://dx.doi.org/10.1101/gad.335836.119 |
Ejemplares similares
-
Nuclear RNA transcript levels modulate nucleocytoplasmic distribution of ALS/FTD-associated protein FUS
por: Tsai, Yueh-Lin, et al.
Publicado: (2022) -
ALS mutations in TLS/FUS disrupt target gene expression
por: Coady, Tristan H., et al.
Publicado: (2015) -
FUS is sequestered in nuclear aggregates in ALS patient fibroblasts
por: Schwartz, Jacob C., et al.
Publicado: (2014) -
Pathogenesis of FUS-associated ALS and FTD: insights from rodent models
por: Nolan, Matthew, et al.
Publicado: (2016) -
FUS mutations dominate TBK1 mutations in FUS/TBK1 double-mutant ALS/FTD pedigrees
por: Brenner, David, et al.
Publicado: (2021)