Ivanchenko Maria G, Megraw Molly
Department of Botany and Plant Pathology, Oregon State University, Corvallis, OR, USA.
Center for Genome Research and Biocomputing, Oregon State University, Corvallis, OR, USA.
Methods Mol Biol. 2018;1830:225-237. doi: 10.1007/978-1-4939-8657-6_13.
Identifying the transcription start sites (TSS) of genes is essential for characterizing promoter regions. Several protocols have been developed to capture the 5' end of transcripts via Cap-Analysis of Gene Expression (CAGE) or linker-ligation strategies such as Paired-End Analysis of Transcription Start Sites (PEAT), but often require large amounts of tissue. More recently, nanoCAGE was developed for sequencing on the Illumina GAIIx to overcome this limitation. In this chapter, we present the nanoCAGE-XL protocol, the first publicly available adaptation of nanoCAGE for sequencing on recent ultra-high-throughput platforms such as Illumina HiSeq-2000. NanoCAGE-XL provides a method for precise transcription start site identification in large eukaryotic genomes, even in cases where input total RNA quantity is very limited.
识别基因的转录起始位点(TSS)对于表征启动子区域至关重要。已经开发了几种方案,通过基因表达的帽分析(CAGE)或接头连接策略(如转录起始位点的双末端分析(PEAT))来捕获转录本的5'末端,但通常需要大量组织。最近,开发了nanoCAGE用于在Illumina GAIIx上进行测序以克服这一限制。在本章中,我们介绍了nanoCAGE-XL方案,这是nanoCAGE首次公开可用的用于在诸如Illumina HiSeq-2000等最新超高通量平台上进行测序适配方案。NanoCAGE-XL提供了一种在大型真核基因组中精确识别转录起始位点的方法,即使在输入总RNA量非常有限的情况下也是如此。