Abstract
ABSTRACT
Viroid-like RNAs (vdlRNAs) are infectious agents characterized by single-stranded circular genomes folding into compact secondary structures, often containing self-cleaving ribozymes involved in replication. Recent metatranscriptomic studies have expanded their diversity across multiple ecological niches and revealed novel vdlRNAs groups with protein-coding capacity, including zeta viruses, characterized by the potential to encode an endless tandem-repeat protein in each polarity strand. However, besides their
in silico
identification, no experimental evidence supported their existence and molecular features. Here, three new zeta viruses were identified and one of them was molecularly characterized from soil. In addition, a novel type of coding vdlRNAs, named betaviroid-like RNAs was discovered. Similar to zeta viruses, betaviroid-like RNAs are circular RNAs containing, in each polarity strand, one ribozyme and one open reading frame (ORF) encompassing the full-length genome. Unlike zeta viruses, betaviroid-like ORFs are not endless but longer than the unit-length genome. Existence of both circular RNA polarity strands, absence of DNA forms, and self-cleavage activity of ribozymes were experimentally confirmed for both zeta viruses and betaviroid-like RNAs, providing data consistent with symmetric rolling-circle replication. Additional zeta viruses and betaviroid-like RNAs were identified in publicly available metatranscriptomic datasets from wetlands of different geographic areas, supporting their broad distribution. Sixteen zeta viruses contain diverse self-cleaving ribozymes, including delta, type II and III hammerhead, twister, and hairpin ribozymes, expanding the known ribozyme diversity of this group. Altogether, our results provide the first experimental characterization of zeta viruses and betaviroid-like RNAs expanding the diversity of circular RNA replicons.
IMPORTANCE
This study supports the existence of two novel groups of protein-coding viroid-like RNAs, further expanding the known diversity and complexity of these agents. In addition to exhibiting the characteristic features of viroid-like RNAs, including circular RNA genomes, compact secondary structures, and self-cleaving ribozymes active in both polarity strands, these molecules possess coding capacity on both strands, with the coding potential exceeding the length of the genomic RNA itself. The coexistence of replication-associated RNA motifs and protein-coding sequences within the same genomic regions points to an extraordinary level of genomic information compression and reveals a previously unrecognized strategy of genome organization. At the same time, these findings raise important questions regarding the origin, evolution, expression, and biological roles of these RNAs, as well as the selective pressures that have shaped such a highly compact genomic architecture.