Institute of Bioorganic Chemistry, Polish Academy of Sciences, Poznań, Poland.
Institute of Human Genetics, Polish Academy of Sciences, Poznań, Poland.
J Biomol Struct Dyn. 2022 Apr;40(7):3038-3045. doi: 10.1080/07391102.2020.1844802. Epub 2020 Nov 17.
A new mechanism of RNA circularization driven by specific binding of miRNAs is described. We identified the 71 CUUCC pentanucleotide motifs distributed regularly throughout the entire molecule of CDR1as RNA that bind to 71 miRNAs through their seed sequence GGAAG. The sequential binding of miR-7 RNAs (71 molecules) brings both ends of CDR1as RNA (1 molecule) together and stimulate phosphodiester bond formation between nucleotides C and A at the 5' and 3' end, respectively. The binding of miRNAs to CDR1as RNA results in the unique complex formation, which shows three specific structural domains: (i) two short helixes with an internal loop, (ii) the hinge, and (iii) the triple-helix. The proposed mechanism explains specific RNA circularization and its function as a miRNAs sponge. Furthermore, the existing wet experimental data on the interaction of CDR1as RNA with miR-7 fully supports our observation. Although miR-671 shows the same seed sequence as miR-7, it forms an almost perfect double helix with CDR1as RNA and induces the cleavage of CDR1as, but does not stimulate circularization. To check how common is the proposed mechanism among circular RNAs, we analyzed the most recent circAtlas database counting almost 1.1 million sequences. It turned out that there are a huge number of circRNAs, which showed miRNAs seed binding sequences distributed through the whole circRNA sequences and prove that circularization of linear transcript is miRNA dependent.Communicated by Ramaswamy H. Sarma.
一种由 miRNAs 特异性结合驱动的 RNA 环化新机制被描述。我们鉴定出 71 个 CUUCC 五核苷酸基序,这些基序均匀分布在 CDR1as RNA 分子的整个分子中,通过其种子序列 GGAAG 与 71 个 miRNA 结合。miR-7 RNA(71 个分子)的顺序结合将 CDR1as RNA 的两端(1 个分子)聚集在一起,并分别刺激 5'和 3'端核苷酸 C 和 A 之间的磷酸二酯键形成。miRNAs 与 CDR1as RNA 的结合导致独特的复合物形成,其显示三个特定的结构域:(i)带有内部环的两个短螺旋,(ii)铰链,和(iii)三螺旋。所提出的机制解释了特定的 RNA 环化及其作为 miRNAs 海绵的功能。此外,关于 CDR1as RNA 与 miR-7 相互作用的现有湿实验数据完全支持我们的观察。尽管 miR-671 显示与 miR-7 相同的种子序列,但它与 CDR1as RNA 形成几乎完美的双链,并诱导 CDR1as 的切割,但不刺激环化。为了检查所提出的机制在环状 RNA 中是多么常见,我们分析了最近的 circAtlas 数据库,其中包含近 110 万个序列。事实证明,有大量的 circRNAs,它们显示 miRNA 种子结合序列分布在整个 circRNA 序列中,并证明线性转录物的环化是 miRNA 依赖性的。由 Ramaswamy H. Sarma 传达。