| Literature DB >> 31532701 |
Xiaoxin Liu1,2, Zhangfeng Hu1, Junfei Zhou1, Cheng Tian1, Guangmei Tian1, Miao He1, Lifen Gao1, Lihong Chen1, Tiantian Li1, Hai Peng1, Weixiong Zhang1,2,3.
Abstract
Formed by back splicing or back fusion of linear RNAs, circular RNAs (circRNAs) constitute a new class of non-coding RNAs of eukaryotes. Recent studies reveal a spliceosome-dependent biogenesis of circRNAs where circRNAs arise at the intron-exon junctions of mRNAs. In this study, using a novel de novo identification method, we show that circRNAs can originate from the interior regions of exons, introns, and intergenic transcripts in human, mouse and rice, which were referred to as interior circRNAs (i-circRNAs). Many i-circRNAs have some remarkable characteristics: multiple i-circRNAs may arise from the same genomic locus; their back fusion points may not be associated with the AG/GT splicing sites, but rather a new pair of motif AC/CT, their back fusion points are adjacent to complementary sequences; and they may circulate on short homologous sequences. We validated several i-circRNAs in HeLa cells by Polymerase Chain Reaction followed by Sanger sequencing. Our results combined showed that i-circRNAs are bona fide circRNAs, indicated novel biogenesis pathways independent of the splicing apparatus, and expanded our understanding of the origin, diversity, and complexity of circRNAs.Entities:
Keywords: PCR; RNA; RNA sequencing; Sanger sequencing; chimeric RNA; circular RNA
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Year: 2019 PMID: 31532701 PMCID: PMC6948956 DOI: 10.1080/15476286.2019.1669391
Source DB: PubMed Journal: RNA Biol ISSN: 1547-6286 Impact factor: 4.652