| Literature DB >> 27739910 |
Chu-Yu Ye1, Xingchen Zhang1, Qinjie Chu1, Chen Liu1, Yongyi Yu1, Weiqin Jiang2, Qian-Hao Zhu3, Longjiang Fan1,4, Longbiao Guo5.
Abstract
Circular RNAs (circRNAs) have been identified in diverse eukaryotic species and are characterized by RNA backsplicing events. Current available methods for circRNA identification are able to determine the start and end locations of circRNAs in the genome but not their full-length sequences. In this study, we developed a method to assemble the full-length sequences of circRNAs using the backsplicing RNA-Seq reads and their corresponding paired-end reads. By applying the method to an rRNA-depleted/RNase R-treated RNA-Seq dataset, we for the first time identified full-length sequences of nearly 3,000 circRNAs in rice. We further showed that alternative circularization of circRNA is a common feature in rice and, surprisingly, found that the junction sites of a large number of rice circRNAs are flanked by diverse non-GT/AG splicing signals while most human exonic circRNAs are flanked by canonical GT/AG splicing signals. Our study provides a method for genome-wide identification of full-length circRNAs and expands our understanding of splicing signals of circRNAs.Entities:
Keywords: Alternative circularization; circular RNAs; full-length circRNAs; rice; splicing signals
Mesh:
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Year: 2016 PMID: 27739910 PMCID: PMC5680721 DOI: 10.1080/15476286.2016.1245268
Source DB: PubMed Journal: RNA Biol ISSN: 1547-6286 Impact factor: 4.652