PLX166356

GSE124834: Toxic C9orf72 poly(PR) binds heterochromatin, disrupts HP1 and causes dsRNA accumulation

• Organsim mouse
• Type RNASEQ
• Target gene
• Project ARCHS4

How G4C2 repeat expansions in C9orf72 cause frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) is not understood. Here, we report the first mouse model to express poly(PR), a dipeptide repeat protein synthesized from expanded G4C2 repeats. Expression of GFP-(PR)50 throughout the mouse brain yielded progressive brain atrophy, neuron5 loss, loss of poly(PR)-positive cells and gliosis, culminating in motor and memory impairments. We found that poly(PR) bound DNA, localized to heterochromatin, and caused abnormal histone methylation, lamin invaginations, decreases in HP1 expression, and disruptions of HP1 liquid phases. These aberrations of histone methylation, lamins and HP1, which regulate heterochromatin structure and gene expression, were accompanied by repetitive element10 expression and double-stranded RNA accumulation. Thus, we uncover new mechanisms by which poly(PR) contributes to c9FTD/ALS pathogenesis. SOURCE: Christopher LinkLink Lab University of Colorado Boulder