Laboratory of Gene Technology, Department of Biosystems, KU Leuven, Leuven, Belgium.
Methods Mol Biol. 2024;2793:207-235. doi: 10.1007/978-1-0716-3798-2_14.
Detailed transcription maps of bacteriophages are not usually explored, limiting our understanding of molecular phage biology and restricting their exploitation and engineering. The ONT-cappable-seq method described here brings phage transcriptomics to the accessible nanopore sequencing platform and provides an affordable and more detailed overview of transcriptional features compared to traditional RNA-seq experiments. With ONT-cappable-seq, primary transcripts are specifically capped, enriched, and prepared for long-read sequencing on the nanopore sequencing platform. This enables end-to-end sequencing of unprocessed transcripts covering both phage and host genome, thus providing insight on their operons. The subsequent analysis pipeline makes it possible to rapidly identify the most important transcriptional features such as transcription start and stop sites. The obtained data can thus provide a comprehensive overview of the transcription by your phage of interest.
详细的噬菌体转录图谱通常不会被探索,这限制了我们对分子噬菌体生物学的理解,并限制了它们的开发和工程应用。本文中描述的 ONT-cappable-seq 方法将噬菌体转录组学引入到可访问的纳米孔测序平台,并提供了比传统 RNA-seq 实验更具成本效益和更详细的转录特征概述。使用 ONT-cappable-seq,可以对原始转录物进行特异性加帽、富集,并在纳米孔测序平台上进行长读测序准备。这使得能够对噬菌体和宿主基因组的未加工转录物进行端到端测序,从而提供关于它们操纵子的信息。随后的分析流程使得快速识别最重要的转录特征(如转录起始和终止位点)成为可能。因此,获得的数据可以全面概述感兴趣的噬菌体的转录情况。