©The Author(s) 2024.
World J Med Genet. Sep 20, 2024; 12(1): 93011
Published online Sep 20, 2024. doi: 10.5496/wjmg.v12.i1.93011
Published online Sep 20, 2024. doi: 10.5496/wjmg.v12.i1.93011
Table 3 Genome-wide identification of circular RNAs: How it began
| Ref. | Genome-wide identification of circRNAs |
| Salzman et al[18], 2012 | Aimed to distinguish cancer-specific exon scrambling events |
| Identified 2748 scrambled isoforms in Hela and H9 embryonic stem cells | |
| Conclusion: 98% of scrambled isoforms represent circRNAs | |
| Jeck et al[8], 2013 | Classified circular transcripts based on their levels of abundance using three stringencies categories (low, medium, high) |
| Conclusion: circRNAs are conserved, stable, and nonrandom products of RNA splicing that could be involved in the control of gene expression | |
| Memczak et al[7], 2013 | Developed a computational method to detect circRNAs |
| Conclusion: circRNAs form a significant class of post-transcriptional regulators | |
| Guo et al[19], 2014 | Identified and quantified human circRNAs from ENCODE Ribozero RNA-seq data |
| Conclusion: Most circRNAs are nonsignificant side-products of splicing error | |
| Zhang et al[20], 2014 | Developed CIRCexplorer to distinguish thousands of circRNAs in humans with p(A)-wloRNase R RNA-seq data |
| Conclusion: Alternative circularization paired with alternative splicing can generate additional circRNAs from one gene, which is suggestive of the new line of complexity in gene regulation |
- Citation: Sharma A, Bansal C, Sharma KL, Kumar A. Circular RNA: The evolving potential in the disease world. World J Med Genet 2024; 12(1): 93011
- URL: https://www.wjgnet.com/2220-3184/full/v12/i1/93011.htm
- DOI: https://dx.doi.org/10.5496/wjmg.v12.i1.93011