Observation of coordinated RNA folding events by systematic cotranscriptional RNA structure probing

被引:7
作者
Szyjka, Courtney E. [1 ]
Strobel, Eric J. [1 ]
机构
[1] Univ Buffalo, Dept Biol Sci, Buffalo, NY 14260 USA
基金
美国国家卫生研究院;
关键词
SELECTIVE 2'-HYDROXYL ACYLATION; PRIMER EXTENSION; SHAPE; RIBOSWITCH; TRANSCRIPTION; RECOGNITION; SPECIFICITY; RESOLUTION; BACTERIA; PROTEIN;
D O I
10.1038/s41467-023-43395-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
RNA begins to fold as it is transcribed by an RNA polymerase. Consequently, RNA folding is constrained by the direction and rate of transcription. Understanding how RNA folds into secondary and tertiary structures therefore requires methods for determining the structure of cotranscriptional folding intermediates. Cotranscriptional RNA chemical probing methods accomplish this by systematically probing the structure of nascent RNA that is displayed from an RNA polymerase. Here, we describe a concise, high-resolution cotranscriptional RNA chemical probing procedure called variable length Transcription Elongation Complex RNA structure probing (TECprobe-VL). We demonstrate the accuracy and resolution of TECprobe-VL by replicating and extending previous analyses of ZTP and fluoride riboswitch folding and mapping the folding pathway of a ppGpp-sensing riboswitch. In each system, we show that TECprobe-VL identifies coordinated cotranscriptional folding events that mediate transcription antitermination. Our findings establish TECprobe-VL as an accessible method for mapping cotranscriptional RNA folding pathways. RNA begins to fold as the nascent transcript emerges from a transcribing RNA polymerase. Here, the authors develop a concise method for mapping RNA folding pathways that couples in vitro transcription with high-throughput RNA chemical probing.
引用
收藏
页数:22
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