PT  - JOURNAL ARTICLE
AU  - Yu Sun
AU  - Aziz Eshov
AU  - Junjie U. Guo
TI  - C9orf72 Dipeptide Repeats Inhibit UPF1-Mediated RNA Decay Independent of Stress Granule Formation
AID  - 10.1101/623769
DP  - 2019 Jan 01
TA  - bioRxiv
PG  - 623769
4099  - http://biorxiv.org/content/early/2019/04/30/623769.short
4100  - http://biorxiv.org/content/early/2019/04/30/623769.full
AB  - Expansion of an intronic (GGGGCC)n repeat region within the C9orf72 gene is a major cause of familial amyotrophic lateral sclerosis and frontotemporal dementia (c9ALS/FTD). A pathological hallmark in c9ALS/FTD is the accumulation of misprocessed RNAs, which are often targets of RNA surveillance pathways in normal cells. Here we show that nonsense-mediated decay (NMD) and other RNA decay mechanisms involving upstream frameshift 1 (UPF1), collectively referred to as UPF1-mediated RNA decay (UMD), are broadly inhibited in c9ALS/FTD brains. These effects are recapitulated in cultured cells by the ectopic expression of arginine-rich dipeptide repeats (DPRs), poly(GR) and poly(PR). Despite these two DPRs causing the recruitment of UPF1 to stress granules, stress granule formation is neither sufficient nor necessary for UMD inhibition. Our results suggest that UMD inhibition may accelerate the accumulation of deleterious RNAs and polypeptides in c9ALS/FTD.