Abstract

Circular DNAs, such as most prokaryotic and phage genomes, are a frequent form of nucleic acids, whereas circular RNAs had been regarded as unusual macromolecules until very recently. The first reported RNA circles were the family of small infectious genomes of viroids and circular RNA (circRNA) satellites of plant viruses, some of which contain small self-cleaving RNA motifs, such as the hammerhead (HHR) and hairpin ribozymes. A similar infectious circRNA, the unique human hepatitis delta virus (HDV), is another viral satellite that also encodes self-cleaving motifs called HDV ribozymes. Very recently, different animals have been reported to contain HDV-like circRNAs with typical HDV ribozymes, but also conserved HHR motifs, as we describe here. On the other hand, eukaryotic and prokaryotic genomes encode sequences able to self-excise as circRNAs, like the autocatalytic Group I and II introns, which are widespread genomic mobile elements. In the 1990s, the first circRNAs encoded in a mammalian genome were anecdotally reported, but their abundance and importance have not been unveiled until recently. These gene-encoded circRNAs are produced by events of alternative splicing in a process generally known as backsplicing. However, we have found a second natural pathway of circRNA expression conserved in numerous plant and animal genomes, which efficiently promotes the accumulation of small non-coding RNA circles through the participation of HHRs. Most of these genome-encoded circRNAs with HHRs are the transposition intermediates of a novel family of non-autonomous retrotransposons called retrozymes, with intriguing potential as new forms of gene regulation.

Highlights

  • Closed circular RNA molecules have been historically regarded as a peculiar form of nucleic acids

  • Both long terminal repeats (LTRs) delimit a central non-protein-coding region (~300–700 bp), which begins with the sequence of a primer binding site (PBS) corresponding to the complementary tRNAMet of the plant, and finishes with a poly-purine tract (PPT), which are both characteristic elements of LTR-retrotransposons [76]

  • Previous bioinformatic searches reported that many metazoan genomes contain thousands of minimal type I HHRs [74], which usually lack any of the non-conserved nucleotides of the helix III (Figure 3). Most of these atypical ribozymes were found as dispersed motifs in non-coding regions of the animal genomes, but in some cases, they mapped to the pseudo-LTRs of Penelope-like retroelements (PLEs) [74]

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Summary

Introduction

Closed circular RNA molecules (circRNAs) have been historically regarded as a peculiar form of nucleic acids. Circular DNAs, such as plasmids or many bacteriophage, viral, plastid and prokaryotic genomes, are ubiquitous molecules among all areas of life This view has changed dramatically in recent years with the discovery of new examples of circRNAs of diverse origin, with intriguing regulatory and biotechnological capabilities. It is somehow surprising that, despite their original discovery more than 40 years ago [2], the abundance and roles of circRNAs in biology have remained poorly studied. Their discovery as an atypical family of minimal subviral genomes, together with the unique biochemical and biophysical features of circRNAs compared with classic linear RNAs, had hindered the interest in the study of RNA circles until recently. RNAs, such as a high stability against exonucleases, a more definite fold, or their capability for an efficient replication by a rolling circle mechanism

The Discovery of the CircRNAs
Genome-Encoded CircRNAs
Autocatalytic RNA Cleavage in Diverse RNA Circles
Three-dimensional of of thethe three possible
Hammerhead Ribozymes in the Genomes of Flowering Plants
Diverse Type I HHRs Occur in Autonomous and in Non-autonomous Metazoan
A general Model for Retrozyme Spreading in Plant and Animal Genomes
Findings
Concluding Remarks
Full Text
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