Abstract

Regulation of post-transcriptional gene expression on mRNA level in eukaryotic cells includes translocation, translation, translational repression, storage, mRNA decay, RNA silencing, and nonsense-mediated decay. These processes are associated with various RNA-binding proteins and cytoplasmic ribonucleoprotein complexes many of which are conserved across eukaryotes. Microscopically visible aggregations formed by ribonucleoprotein complexes are termed RNA granules. Stress granules where the translationally inactive mRNAs are stored and processing bodies where mRNA decay may occur present the most studied RNA granule types. Diverse RNP-granules are increasingly being assigned important roles in viral infections. Although the majority of the molecular level studies on the role of RNA granules in viral translation and replication have been conducted in mammalian systems, some studies link also plant virus infection to RNA granules. An increasing body of evidence indicates that plant viruses require components of stress granules and processing bodies for their replication and translation, but how extensively the cellular mRNA regulatory network is utilized by plant viruses has remained largely enigmatic. Antiviral RNA silencing, which is an important regulator of viral RNA stability and expression in plants, is commonly counteracted by viral suppressors of RNA silencing. Some of the RNA silencing suppressors localize to cellular RNA granules and have been proposed to carry out their suppression functions there. Moreover, plant nucleotide-binding leucine-rich repeat protein-mediated virus resistance has been linked to enhanced processing body formation and translational repression of viral RNA. Many interesting questions relate to how the pathways of antiviral RNA silencing leading to viral RNA degradation and/or repression of translation, suppression of RNA silencing and viral RNA translation converge in plants and how different RNA granules and their individual components contribute to these processes. In this review we discuss the roles of cellular RNA regulatory mechanisms and RNA granules in plant virus infection in the light of current knowledge and compare the findings to those made in animal virus studies.

Highlights

  • Endogenous mRNAs produced in the nucleus of eukaryotic cells are subsequently exported to the cytoplasm for protein synthesis

  • Enhancer of decapping, involved in translational repression 5′–3′ exonuclease Translational repression, processing bodies (PBs) dynamics, promotes mRNA decay Enhancers of decapping, promotion of PB assembly Activates decapping and inhibits translation miRNA-dependent endonuclease Interacts with AGO proteins in PBs to promote translational repression by miRNAs (Possible functional analog of GW182) Involved in nonsense-mediated mRNA decay processes Decapping activator, endogenous silencing suppressor Tandem zinc-finger protein, RNA delivery and protein recruitment into PBs and stress granules (SGs)

  • Plant RR-tandem zinc finger proteins (TZF) are involved in biotic stress responses potentially by binding to specific elements of the corresponding mRNAs and recruiting the assembled messenger ribonucleoprotein (mRNP) complexes into PBs and SGs, no report has linked them to regulation of virus infection in plant cells so far

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Summary

Introduction

Endogenous mRNAs produced in the nucleus of eukaryotic cells are subsequently exported to the cytoplasm for protein synthesis. Enhancer of decapping, involved in translational repression 5′–3′ exonuclease Translational repression, PB dynamics, promotes mRNA decay (for retroviruses required for replication and encapsidation) Enhancers of decapping, promotion of PB assembly Activates decapping and inhibits translation miRNA-dependent endonuclease Interacts with AGO proteins in PBs to promote translational repression by miRNAs (Possible functional analog of GW182) Involved in nonsense-mediated mRNA decay processes Decapping activator, endogenous silencing suppressor Tandem zinc-finger protein, RNA delivery and protein recruitment into PBs and SGs

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