2015
DOI: 10.1016/j.canlet.2015.06.003
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Circular RNA: A new star of noncoding RNAs

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Cited by 1,430 publications
(1,095 citation statements)
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References 69 publications
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“…It has been proposed that circRNAs may act as competing endogenous RNAs to bind proteins (protein sponges) [30,31]. Then, we focused on the sequence of hsa_circ_0001649 to find its potential RNA-binding proteins (RBPs) binding sites (starBase v2.0) [32], and we found that hsa_circ_0001649 had 6 potential protein binding sites for U2 auxiliary factor 65 kDa subunit (U2AF65), 5 potential protein binding sites for Eukaryotic initiation factor 4A-III (EIF4A3), and 1 potential protein binding site for Regulator of nonsense transcripts 1 (UPF1).…”
Section: Discussionmentioning
confidence: 99%
“…It has been proposed that circRNAs may act as competing endogenous RNAs to bind proteins (protein sponges) [30,31]. Then, we focused on the sequence of hsa_circ_0001649 to find its potential RNA-binding proteins (RBPs) binding sites (starBase v2.0) [32], and we found that hsa_circ_0001649 had 6 potential protein binding sites for U2 auxiliary factor 65 kDa subunit (U2AF65), 5 potential protein binding sites for Eukaryotic initiation factor 4A-III (EIF4A3), and 1 potential protein binding site for Regulator of nonsense transcripts 1 (UPF1).…”
Section: Discussionmentioning
confidence: 99%
“…CircRNA-targeted miRNA-gene network was constructed using Targetscan and miRanda. CircRNAs contain many miRNA response elements (MREs) [33], we then selected the top 5 predicted miRNA targets of 3 randomly differentially upregulated circRNAs (chr5: 51521674-51524828, chr3: 3137166-3138170 +, chr4: 59505289-59510641-) in tumor liver samples, meanwhile, the top 10 target genes for each miRNA were collected. Finally, the integrated circRNA-targeted miRNA-gene network was determined ( Figure 6).…”
Section: Mirna Binding Sites Prediction and Circrnatargeted Mirna-genmentioning
confidence: 99%
“…They are widely expressed in mammalian cells and play crucial roles in the regulation of gene expression at the transcriptional or post-transcriptional levels [3, 4] . Compared with traditional linear RNA, circRNAs do not have the free 3′ or 5′ ends, but form covalently closed continuous loops [5, 6]. This confers resistance to RNase R treatment, allowing circRNAs to be selectively enriched during sample processing and making them more suitable biomarkers than other types of RNA [7-9].…”
Section: Introductionmentioning
confidence: 99%