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A cap 0-dependent mRNA capture method to analyze the yeast transcriptome.

Martyna NowackaPrzemyslaw LatochMatylda A IzertNatalia K KarolakRafal TomeckiMichał KoperAgnieszka TudekAgata L StarostaMaria Wiktoria Górna
Published in: Nucleic acids research (2022)
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.
Keyphrases
  • rna seq
  • single cell
  • binding protein
  • saccharomyces cerevisiae
  • gene expression
  • protein protein
  • endothelial cells
  • amino acid
  • genome wide
  • cancer therapy
  • healthcare
  • dna methylation
  • big data