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

Author:

Barrett Steven P1,Wang Peter L12,Salzman Julia12

Affiliation:

1. Department of Biochemistry, Stanford University School of Medicine, Stanford, United States

2. Stanford Cancer Institute, Stanford University School of Medicine, Stanford, United States

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.

Funder

National Cancer Institute (NCI)

Donald E. and Delia B. Baxter Foundation

Stanford University

Lucille P. Markey Charitable Trust

Alfred P. Sloan Foundation

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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