Abstract

Circular RNAs (circRNAs) are the products of the non-canonical splicing of pre-mRNAs. In contrast to humans and animals, our knowledge of the biogenesis and function of circRNAs in plants is very scarce. To identify proteins involved in plant circRNA generation, we characterized the transcriptomes of 18 Arabidopsis thaliana knockout mutants for genes related to splicing. The vast majority (>90%) of circRNAs were formed in more than one variant; only a small fraction of circRNAs was mutant-specific. Five times more circRNA types were identified in cbp80 and three times more in c2h2 mutants than in the wild-type. We also discovered that in cbp80, c2h2 and flk mutants, the accumulation of circRNAs was significantly increased. The increased accumulation of circular transcripts was not accompanied by corresponding changes in the accumulation of linear transcripts. Our results indicate that one of the roles of CBP80, C2H2 and FLK in splicing is to ensure the proper order of the exons. In the absence of one of the above-mentioned factors, the process might be altered, leading to the production of circular transcripts. This suggests that the transition toward circRNA production can be triggered by factors sequestering these proteins. Consequently, the expression of linear transcripts might be regulated through circRNA production.

Highlights

  • Circular RNAs are a class of non-coding alternatively spliced RNA transcripts

  • We analyzed circRNA and mRNA accumulation in wild-type A. thaliana and its selected mutants that had changes in the genes involved in splicing

  • Thaliana variant selection led us to a list of 86 mutants with changes in genes related to splicing, of which 23 had a precisely described phenotype

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Summary

Introduction

Circular RNAs (circRNAs) are a class of non-coding alternatively spliced RNA transcripts. It has been shown that circRNAs are present across the eukaryotic tree of life [1]. Many of them are evolutionarily conserved and highly abundant [2,3] These facts, together with the newest findings on some circRNA functions [4,5,6], strongly suggest important the roles of circRNAs in crucial cellular processes, especially in the regulation of gene expression [7]. CircRNAs may act as protein-binding molecules [7,8,9] or miRNA sponges [6,9,10]. CDR1as/ciRS−7 and Sry circRNAs have many miRNA-binding sites, via which they sequester miRNA from its target sites in mRNA. The facts listed above permit us to hypothesize that in addition to the protein/RNA factors involved in canonical

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