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塞丽娜:基于 ceRNA 相互作用的综合分析进行系统的 circRNA 功能注释。

Cerina: systematic circRNA functional annotation based on integrative analysis of ceRNA interactions.

机构信息

Baylor Scott & White Research Institute, Dallas, TX, 75204, USA.

出版信息

Sci Rep. 2020 Dec 17;10(1):22165. doi: 10.1038/s41598-020-78469-x.

Abstract

Circular RNAs, a family of covalently circularized RNAs with tissue-specific expression, were recently demonstrated to play important roles in mammalian biology. Regardless of extensive research to predict, quantify, and annotate circRNAs, our understanding of their functions is still in its infancy. In this study, we developed a novel computational tool: Competing Endogenous RNA for INtegrative Annotations (Cerina), to predict biological functions of circRNAs based on the competing endogenous RNA model. Pareto Frontier Analysis was employed to integrate ENCODE mRNA/miRNA data with predicted microRNA response elements to prioritize tissue-specific ceRNA interactions. Using data from several circRNA-disease databases, we demonstrated that Cerina significantly improved the functional relevance of the prioritized ceRNA interactions by several folds, in terms of precision and recall. Proof-of-concept studies on human cancers and cardiovascular diseases further showcased the efficacy of Cerina on predicting potential circRNA functions in human diseases.

摘要

环状 RNA 是一类具有组织特异性表达的共价闭环 RNA,最近被证明在哺乳动物生物学中发挥着重要作用。尽管已经进行了广泛的研究来预测、定量和注释 circRNA,但我们对其功能的理解仍处于起步阶段。在这项研究中,我们开发了一种新的计算工具:基于竞争性内源性 RNA 模型的整合注释的竞争性内源性 RNA(Cerina),用于预测 circRNA 的生物学功能。采用 Pareto 前沿分析将 ENCODE mRNA/miRNA 数据与预测的 microRNA 反应元件整合,以优先考虑组织特异性 ceRNA 相互作用。使用来自几个 circRNA 疾病数据库的数据,我们证明 Cerina 显著提高了优先 ceRNA 相互作用的功能相关性,在精度和召回率方面都有了几个数量级的提升。在人类癌症和心血管疾病的概念验证研究中,Cerina 进一步展示了其在预测人类疾病中潜在 circRNA 功能方面的有效性。

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