An Insect Viral Protein Disrupts Stress Granule Formation in Mammalian Cells

• Published in: Journal of molecular biology Vol. 435; no. 16; p. 168042
• Main Authors: Sadasivan, Jibin, Hyrina, Anastasia, DaSilva, Rachel, Jan, Eric
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Ltd 15.08.2023
• Subjects: dicistrovirus; RNA; RNA transport; stress granules; virus; stress granules; RNA; RNA transport; virus; dicistrovirus
• ISSN: 0022-2836; 1089-8638
• DOI: 10.1016/j.jmb.2023.168042

Generated using Biorender.com. [Display omitted] •Expression of an insect viral protein (CrPV-1A) blocks SG formation in HeLa cells.•CrPV-1A localizes to the nuclear periphery and induces poly(A)+ RNA accumulation in the nucleus.•CrPV-1A expression inhibits pathologic aggregation of TDP-43 and FUS proteins. Stress granules (SGs) are cytosolic RNA-protein aggregates assembled during stress-induced translation arrest. Virus infection, in general, modulates and blocks SG formation. We previously showed that the model dicistrovirus Cricket paralysis virus (CrPV) 1A protein blocks stress granule formation in insect cells, which is dependent on a specific arginine 146 residue. CrPV-1A also inhibits SG formation in mammalian cells suggesting that this insect viral protein may be acting on a fundamental process that regulates SG formation. The mechanism underlying this process is not fully understood. Here, we show that overexpression of wild-type CrPV-1A, but not the CrPV-1A(R146A) mutant protein, inhibits distinct SG assembly pathways in HeLa cells. CrPV-1A mediated SG inhibition is independent of the Argonaute-2 (Ago-2) binding domain and the E3 ubiquitin ligase recruitment domain. CrPV-1A expression leads to nuclear poly(A)+ RNA accumulation and is correlated with the localization of CrPV-1A to the nuclear periphery. Finally, we show that the overexpression of CrPV-1A blocks FUS and TDP-43 granules, which are pathological hallmarks of neurodegenerative diseases. We propose a model whereby CrPV-1A expression in mammalian cells blocks SG formation by depleting cytoplasmic mRNA scaffolds via mRNA export inhibition. CrPV-1A provides a new molecular tool to study RNA-protein aggregates and potentially uncouple SG functions.