A trans-activator-like structure in RCNMV RNA1 evokes the origin of the trans-activator in RNA2

• Published in: PLoS pathogens Vol. 16; no. 1; p. e1008271
• Main Authors: Newburn, Laura R, White, K Andrew
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 01-01-2020; Public Library of Science (PLoS)
• Subjects: Annotations; Binding sites; Biology and life sciences; Cucumis sativus; DNA-directed RNA polymerase; Evolution; Evolution, Molecular; Genome, Viral; Genomes; Nucleic Acid Conformation; Packaging; Plant viruses; Proteins; Red clover; Replication; Research and analysis methods; RNA polymerase; RNA viruses; RNA, Viral - chemistry; RNA, Viral - physiology; Segments; Structure-Activity Relationship; Structure-function relationships; Tombusviridae - genetics; Tombusviridae - physiology; Trans-Activators - physiology; Transcription; Virus Assembly; Viruses; Toronto Ontario Canada; Canada
• ISSN: 1553-7374; 1553-7366; 1553-7374
• DOI: 10.1371/journal.ppat.1008271

The Red clover necrotic mosaic virus (RCNMV) genome consists of two plus-strand RNA genome segments, RNA1 and RNA2. RNA2 contains a multifunctional RNA structure known as the trans-activator (TA) that (i) promotes subgenomic mRNA transcription from RNA1, (ii) facilitates replication of RNA2, and (iii) mediates particle assembly and copackaging of genome segments. The TA has long been considered a unique RNA element in RCNMV. However, by examining results from RCNMV genome analyses in the ViRAD virus (re-)annotation database, a putative functional RNA element in the polymerase-coding region of RNA1 was identified. Structural and functional analyses revealed that the novel RNA element adopts a TA-like structure (TALS) and, similar to the requirement of the TA for RNA2 replication, the TALS is necessary for the replication of RNA1. Both the TA and TALS possess near-identical asymmetrical internal loops that are critical for efficient replication of their corresponding genome segments, and these structural motifs were found to be functionally interchangeable. Moreover, replacement of the TA in RNA2 with a stabilized form of the TALS directed both RNA2 replication and packaging of both genome segments. Based on their comparable properties and considering evolutionary factors, we propose that the TALS appeared de novo in RNA1 first and, subsequently, the TA arose de novo in RNA2 as a functional mimic of the TALS. This and other related information were used to formulate a plausible evolutionary pathway to describe the genesis of the bi-segmented RCNMV genome. The resulting scenario provides an evolutionary framework to further explore and test possible origins of this segmented RNA plant virus.