Abstract

Bamboo mosaic virus (BaMV), which belongs to the genus Potexvirus in the family Alphaflexiviridae, has a single-stranded positive-sense RNA genome that is approximately 6400 nucleotides (nts) in length. Positive-sense RNA viruses can use genomic RNA as a template for translation and replication after entering a suitable host cell. Furthermore, such viral RNA is recognized by capsid protein for packaging and by viral movement protein(s) or the movement protein complex for cell-to-cell and systemic movement. Hence, viral RNA must contain signals for different functions to complete the viral infection cycle. In this review, we examine various cis-acting elements in the genome of BaMV. The highly structured 3′ untranslated region (UTR) of the BaMV genomic RNA plays multiple roles in the BaMV infection cycle, including targeting chloroplasts for RNA replication, providing an initiation site for the synthesis of minus-strand RNA, signaling for polyadenylation, and directing viral long-distance movement. The nt at the extreme 3′ end and the structure of the 3′-terminus of minus-strand RNA are involved in the initiation of plus-strand genomic RNA synthesis. Both these regions have been mapped and reported to interact with the viral-encoded RNA-dependent RNA polymerase. Moreover, the sequences upstream of open reading frames (ORFs) 2, 3, and 5 are involved in regulating subgenomic RNA synthesis. The cis-acting elements that were identified in BaMV RNA are discussed and compared with those of other potexviruses.

Highlights

  • For a positive-sense RNA virus to establish a successful infection in a host, the viral RNA must house diverse cis-acting elements for minus-strand, plus-strand, and possibly subgenomic RNA syntheses (Dreher, 1999; Newburn and White, 2015)

  • For accomplishing an efficient infection by a positive-sense RNA virus, the viral genome consists of various cis-acting elements for intracellular trafficking to organellar membranous target sites, minus-strand RNA synthesis, plus-strand genomic RNA synthesis, subgenomic RNA synthesis, viral movements, and viral encapsidation

  • We summarize studies of most of the cis-acting elements identified in the Bamboo mosaic virus (BaMV) genome, except for those involved in viral movement and viral encapsidation

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Summary

INTRODUCTION

For a positive-sense RNA virus to establish a successful infection in a host, the viral RNA must house diverse cis-acting elements for minus-strand, plus-strand, and possibly subgenomic RNA syntheses (Dreher, 1999; Newburn and White, 2015). Cis-acting elements could be involved in cell-to-cell or systemic movement and encapsidation of viral RNA (Kwon et al, 2005; Lough et al, 2006; Cho et al, 2012; Rossmann, 2013). A few approaches were used to determine the minimum length and structures of viral cis-acting elements required for various functions. The difficulty involved in isolating a competent replicase preparation that can synthesize minus- or plus-strand RNAs, with the cis-acting elements provided, limits. Cis-acting Elements in BaMV RNA Genome its use. The structured cis-acting elements must be functionally verified by mutational analysis in either an in vitro replication assay or an in vivo infection assay. The cis-acting elements of BaMV RNA involved in viral RNA replication, intracellular trafficking, and movement have been extensively studied in the last two decades. This report comprehensively reviews these studies and discusses the common theme of the roles of these cis-acting elements that could be applied to other members of potexvirus including the Potato virus X (PVX), one of the top 10 plant viruses in molecular plant pathology (Scholthof et al, 2011), and even to certain animal viruses of Alphaviruses

VIRAL RNA INTRACELLULAR TRAFFICKING
Findings
SUBGENOMIC RNA SYNTHESIS
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