| Literature DB >> 33288960 |
Siqi Li1, Xiang Li1, Wei Xue2, Lin Zhang3, Liang-Zhong Yang1, Shi-Meng Cao1, Yun-Ni Lei2,4, Chu-Xiao Liu1, Si-Kun Guo1, Lin Shan1, Man Wu1, Xiao Tao1, Jia-Lin Zhang1,5, Xiang Gao1,4, Jun Zhang1, Jia Wei2, Jinsong Li6,7,8, Li Yang9,10, Ling-Ling Chen11,12,13.
Abstract
Circular RNAs (circRNAs) produced from back-spliced exons are widely expressed, but individual circRNA functions remain poorly understood owing to the lack of adequate methods for distinguishing circRNAs from cognate messenger RNAs with overlapping exons. Here, we report that CRISPR-RfxCas13d can effectively discriminate circRNAs from mRNAs by using guide RNAs targeting sequences spanning back-splicing junction (BSJ) sites featured in RNA circles. Using a lentiviral library that targets sequences across BSJ sites of highly expressed human circRNAs, we show that a group of circRNAs are important for cell growth mostly in a cell-type-specific manner and that a common oncogenic circRNA, circFAM120A, promotes cell proliferation by preventing the mRNA for family with sequence similarity 120A (FAM120A) from binding the translation inhibitor IGF2BP2. Further application of RfxCas13d-BSJ-gRNA screening has uncovered circMan1a2, which has regulatory potential in mouse embryo preimplantation development. Together, these results establish CRISPR-RfxCas13d as a useful tool for the discovery and functional study of circRNAs at both individual and large-scale levels.Entities:
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Year: 2020 PMID: 33288960 DOI: 10.1038/s41592-020-01011-4
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 47.990