Biological and Chemical Research Centre, Department of Chemistry, University of Warsaw, Warsaw, Warsaw 02-093, Poland.
Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Warsaw 02-106, Poland.
Nucleic Acids Res. 2022 Dec 9;50(22):e132. doi: 10.1093/nar/gkac903.
Analysis of the protein coding transcriptome by the RNA sequencing requires either enrichment of the desired fraction of coding transcripts or depletion of the abundant non-coding fraction consisting mainly of rRNA. We propose an alternative mRNA enrichment strategy based on the RNA-binding properties of the human IFIT1, an antiviral protein recognizing cap 0 RNA. Here, we compare for Saccharomyces cerevisiae an IFIT1-based mRNA pull-down with yeast targeted rRNA depletion by the RiboMinus method. IFIT1-based RNA capture depletes rRNA more effectively, producing high quality RNA-seq data with an excellent coverage of the protein coding transcriptome, while depleting cap-less transcripts such as mitochondrial or some non-coding RNAs. We propose IFIT1 as a cost effective and versatile tool to prepare mRNA libraries for a variety of organisms with cap 0 mRNA ends, including diverse plants, fungi and eukaryotic microbes.
通过 RNA 测序分析蛋白质编码转录组需要富集所需的编码转录本部分,或者去除主要由 rRNA 组成的丰富的非编码部分。我们提出了一种基于人 IFIT1 的 RNA 结合特性的替代 mRNA 富集策略,IFIT1 是一种识别帽 0 RNA 的抗病毒蛋白。在这里,我们比较了酵母中基于 IFIT1 的 mRNA 下拉与 RiboMinus 方法靶向酵母 rRNA 耗竭的方法。基于 IFIT1 的 RNA 捕获更有效地去除 rRNA,产生高质量的 RNA-seq 数据,对蛋白质编码转录组具有极好的覆盖度,同时去除无帽转录本,如线粒体或一些非编码 RNA。我们提出 IFIT1 是一种具有成本效益且用途广泛的工具,可用于制备具有帽 0 mRNA 末端的各种生物体的 mRNA 文库,包括各种植物、真菌和真核微生物。