Screening for functional circular RNAs using the CRISPR–Cas13 system

清脆的 生物 环状RNA 计算生物学 外显子 RNA剪接 核糖核酸 翻译(生物学) 遗传学 选择性拼接 信使核糖核酸 细胞生物学 基因
作者
Siqi Li,Xiang Li,Wei Xue,Lin Zhang,Liang-Zhong Yang,Shi-Meng Cao,Yun-Ni Lei,Chu‐Xiao Liu,Si-Kun Guo,Lin Shan,Man Wu,Xiao Tao,Jialin Zhang,Xiang Gao,Jun Zhang,Jia Wei,Jinsong Li,Li Yang,Ling‐Ling Chen
出处
期刊:Nature Methods [Springer Nature]
卷期号:18 (1): 51-59 被引量:239
标识
DOI:10.1038/s41592-020-01011-4
摘要

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.
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