Human FUS Protein Suppresses the Production of Toxic Repeat Polypeptides that Cause Neurodegenerative Diseases -- Kindai University
Now, Japanese researchers have discovered a key regulatory mechanism involved in C9orf72-linked amyotrophic lateral sclerosis (ALS)/ frontotemporal dementia (FTD) (C9-ALS/FTD). Their findings indicate that in C9-ALS/FTD, the human FUS protein can interact with RNAs containing GGGGCC repeats and suppress their translation by altering their three-dimensional structures, inhibiting neurodegeneration.