
IRIS: A method for predicting in vivo RNA secondary structures using PARIS data
Author(s) -
Zhou Jianyu,
Li Pan,
Zeng Wanwen,
Ma Wenxiu,
Lu Zhipeng,
Jiang Rui,
Cliff Zhang Qiangfeng,
Jiang Tao
Publication year - 2020
Publication title -
quantitative biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.707
H-Index - 15
eISSN - 2095-4697
pISSN - 2095-4689
DOI - 10.1007/s40484-020-0223-4
Subject(s) - rna , nucleic acid secondary structure , computational biology , protein secondary structure , nucleic acid structure , computer science , iris (biosensor) , biology , artificial intelligence , genetics , gene , biochemistry , biometrics
Background RNA secondary structures play a pivotal role in posttranscriptional regulation and the functions of non‐coding RNAs, yet in vivo RNA secondary structures remain enigmatic. PARIS (Psoralen Analysis of RNA Interactions and Structures) is a recently developed high‐throughput sequencing‐based approach that enables direct capture of RNA duplex structures in vivo . However, the existence of incompatible, fuzzy pairing information obstructs the integration of PARIS data with the existing tools for reconstructing RNA secondary structure models at the single‐base resolution. Methods We introduce IRIS, a method for predicting RNA secondary structure ensembles based on PARIS data. IRIS generates a large set of candidate RNA secondary structure models under the guidance of redistributed PARIS reads and then uses a Bayesian model to identify the optimal ensemble, according to both thermodynamic principles and PARIS data. Results The predicted RNA structure ensembles by IRIS have been verified based on evolutionary conservation information and consistency with other experimental RNA structural data. IRIS is implemented in Python and freely available at http://iris.zhanglab.net . Conclusion IRIS capitalizes upon PARIS data to improve the prediction of in vivo RNA secondary structure ensembles. We expect that IRIS will enhance the application of the PARIS technology and shed more insight on in vivo RNA secondary structures.