Pockalny Megan C, Lo Hei-Yong G, Goering Raeann, Taliaferro J Matthew
Department of Biochemistry and Molecular Genetics, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
RNA Bioscience Initiative, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Bio Protoc. 2025 Aug 5;15(15):e5403. doi: 10.21769/BioProtoc.5403.
Thousands of RNAs are localized to specific subcellular locations, and these localization patterns are often required for optimal cell function. However, the sequences within RNAs that direct their transport are unknown for almost all localized transcripts. Similarly, the RNA content of most subcellular locations remains unknown. To facilitate the study of subcellular transcriptomes, we developed the RNA proximity labeling method OINC-seq. OINC-seq utilizes photoactivatable, spatially restricted RNA oxidation to specifically label RNA in proximity to a subcellularly localized bait protein. After labeling, these oxidative RNA marks are then read out via high-throughput sequencing due to their ability to induce predictable misincorporation events by reverse transcriptase. These induced mutations are then quantitatively assessed for each gene using our software package PIGPEN. The observed mutation rate for a given RNA species is therefore related to its proximity to the localized bait protein. This protocol describes procedures for assaying RNA localization via OINC-seq experiments as well as computational procedures for analyzing the resulting data using PIGPEN. Key features • OINC-seq assays the RNA content of a variety of subcellular locations. • OINC-seq utilizes a photoactivatable, proximity-dependent RNA oxidation reaction to label RNAs. • Oxidative RNA marks are read using high-throughput sequencing without the need for enrichment. • Oxidative RNA marks are identified and quantified using the associated PIGPEN software.
数千种RNA定位于特定的亚细胞位置,而这些定位模式通常是细胞最佳功能所必需的。然而,几乎所有定位转录本中指导其运输的RNA序列尚不清楚。同样,大多数亚细胞位置的RNA含量也仍然未知。为了促进对亚细胞转录组的研究,我们开发了RNA邻近标记方法OINC-seq。OINC-seq利用可光激活的、空间受限的RNA氧化来特异性标记与亚细胞定位诱饵蛋白邻近的RNA。标记后,由于这些氧化RNA标记能够诱导逆转录酶产生可预测的错掺入事件,因此通过高通量测序来读取它们。然后使用我们的软件包PIGPEN对每个基因的这些诱导突变进行定量评估。因此,给定RNA种类的观察到的突变率与其与定位诱饵蛋白的接近程度相关。本方案描述了通过OINC-seq实验检测RNA定位的程序以及使用PIGPEN分析所得数据的计算程序。关键特性 • OINC-seq可检测多种亚细胞位置的RNA含量。 • OINC-seq利用可光激活的、邻近依赖性RNA氧化反应来标记RNA。 • 使用高通量测序读取氧化RNA标记,无需富集。 • 使用相关的PIGPEN软件识别和定量氧化RNA标记。