Circular RNA biogenesis can proceed through an exon-containing lariat precursor

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Abstract
Pervasive expression of circular RNA is a recently discovered feature of eukaryotic gene expression programs, yet its function remains largely unknown. The presumed biogenesis of these RNAs involves a non-canonical ‘backsplicing’ event. Recent studies in mammalian cell culture posit that backsplicing is facilitated by inverted repeats flanking the circularized exon(s). Although such sequence elements are common in mammals, they are rare in lower eukaryotes, making current models insufficient to describe circularization. Through systematic splice site mutagenesis and the identification of splicing intermediates, we show that circular RNA in Schizosaccharomyces pombe is generated through an exon-containing lariat precursor. Furthermore, we have performed high-throughput and comprehensive mutagenesis of a circle-forming exon, which enabled us to discover a systematic effect of exon length on RNA circularization. Our results uncover a mechanism for circular RNA biogenesis that may account for circularization in genes that lack noticeable flanking intronic secondary structure.
Funding Information
  • National Cancer Institute (NCI) (R00, CA168987-03)
  • Donald E. and Delia B. Baxter Foundation
  • Stanford University (Stanford Graduate Fellowship)
  • Lucille P. Markey Charitable Trust (Lucille P. Markey Biomedical Research Fellowship)
  • Alfred P. Sloan Foundation