Abstract

Comparison of gene silencing in tissues and whole organisms shows intriguing similarities between plants and animals (Cohen and Xiong, 2011; Hyun et al., 2011; Jose et al., 2011; Melnyk et al., 2011; Molnar et al., 2011) despite that they are very different from each other in many aspects related to the cell-to-cell communications (Ritzenthaler, 2011). Interestingly, one of the shared mechanisms is the reprogramming of intracellular silencing pathways and intercellular communications during development of virus infections. As a part of their counter-defensive strategy, viruses encode silencing suppressors to inhibit various stages of the silencing process. These suppressors are diverse in sequence and structure and act via different molecular mechanisms including, particularly, blockage of intercellular and systemic spread of mobile small interfering RNAs (siRNAs; Li and Ding, 2006; Bivalkar-Mehla et al., 2011; Burgyan and Havelda, 2011; Shimura and Pantaleo, 2011; Song et al., 2011). Importantly, plant, insect, and animal virus suppressors can substitute for each other in different eukaryotic model systems (Schnettler et al., 2008; Jing et al., 2011; Maliogka et al., 2012; Zhu et al., 2012). Many viral proteins that in the past were characterized as proteins involved in systemic plant invasion are now known to be suppressors of gene silencing. For example, tombusvirus P19 blocks the intercellular movement of the silencing signal by binding DCL4-dependent 21-nt siRNA. Cucumovirus 2b protein inhibits the systemic movement of RNA silencing by either binding dsRNA/siRNA or inhibiting the slicer activity of AGO1. Potato virus X P25 protein also inhibits the systemic movement of RNA silencing (Li and Ding, 2006; Burgyan and Havelda, 2011; Shimura and Pantaleo, 2011). Direct link between the viral suppressor activity and the ability of virus to move cell-to-cell and long-distance is further strengthened by the discovery of plant movement proteins (MPs) acting also as silencing suppressors (Bayne et al., 1995; Voinnet et al., 1999; Yaegashi et al., 2007; Powers et al., 2008; Lim et al., 2010; Wu et al., 2010; Senshu et al., 2011; Renovell et al., 2012). On the other hand, it has been shown that the MPs of certain viruses act as viral enhancers of RNA silencing by promoting the propagation of RNA silencing from cell to cell (Vogler et al., 2008; Zhou et al., 2008; Lacombe et al., 2010; Amari et al., 2012).

Highlights

  • We present here a hypothetical model of how interaction of plant viruses with the silencing machinery may contribute to the triple gene block (TGB) origin and evolution during adaptation of viruses to land plant hosts

  • The hypothesis was stimulated by the previous evidence indicating that the suppression of silencing by TGB1 protein encoded by potex- and carlaviruses is not sufficient to allow virus movement between cells, and there must be another function of this protein independent of silencing but required for cellto-cell movement (Bayne et al, 1995; Lim et al, 2010; Senshu et al, 2011)

  • Two additional Chara australis virus (CAV) ORFs code for non-replicative RNA helicase and a protein of unknown function. This CAV helicase is related to CI helicase (SF-II) of Ipomoviruses, which is involved in cell-to-cell movement in addition to replication (Wei et al, 2010)

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Summary

Introduction

To TGB-containing viruses, suppression of local RNA silencing is not sufficient to promote cell-to-cell movement of Turnip crinkle virus (Shi et al, 2009). We can propose that plus-RNA viruses of unicellular algae in the course of transition of hosts to multicellularity may evolve additional RNA helicase genes (either by shuffling with distantly related viruses or by duplication of helicase domain in own replicase) required for virus genome spread over the plant organism (Figure 1).

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