KARR-seq reveals cellular higher-order RNA structures and RNA–RNA interactions

Author:

Wu TongORCID,Cheng Anthony Youzhi,Zhang Yuexiu,Xu Jiayu,Wu JinjunORCID,Wen Li,Li Xiao,Liu Bei,Dou Xiaoyang,Wang Pingluan,Zhang Linda,Fei JingyiORCID,Li Jianrong,Ouyang ZhengqingORCID,He ChuanORCID

Abstract

AbstractRNA fate and function are affected by their structures and interactomes. However, how RNA and RNA-binding proteins (RBPs) assemble into higher-order structures and how RNA molecules may interact with each other to facilitate functions remain largely unknown. Here we present KARR-seq, which uses N3-kethoxal labeling and multifunctional chemical crosslinkers to covalently trap and determine RNA–RNA interactions and higher-order RNA structures inside cells, independent of local protein binding to RNA. KARR-seq depicts higher-order RNA structure and detects widespread intermolecular RNA–RNA interactions with high sensitivity and accuracy. Using KARR-seq, we show that translation represses mRNA compaction under native and stress conditions. We determined the higher-order RNA structures of respiratory syncytial virus (RSV) and vesicular stomatitis virus (VSV) and identified RNA–RNA interactions between the viruses and the host RNAs that potentially regulate viral replication.

Funder

Howard Hughes Medical Institute

U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute

U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences

Publisher

Springer Science and Business Media LLC

Subject

Biomedical Engineering,Molecular Medicine,Applied Microbiology and Biotechnology,Bioengineering,Biotechnology

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