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

Author:

Nowacka Martyna1,Latoch Przemysław23ORCID,Izert Matylda A1,Karolak Natalia K14,Tomecki Rafal25,Koper Michał5,Tudek Agnieszka2,Starosta Agata L2ORCID,Górna Maria W1ORCID

Affiliation:

1. Biological and Chemical Research Centre, Department of Chemistry, University of Warsaw , Warsaw , Warsaw 02-093, Poland

2. Institute of Biochemistry and Biophysics, Polish Academy of Sciences , Warsaw , Warsaw 02-106, Poland

3. Polish-Japanese Academy of Information Technology , Warsaw , Warsaw 02-008, Poland

4. Nencki Institute of Experimental Biology, Polish Academy of Sciences , Warsaw , Warsaw 02-093, Poland

5. Institute of Genetics and Biotechnology, Faculty of Biology, University of Warsaw , Warsaw , Warsaw 02-106, Poland

Abstract

Abstract 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.

Funder

National Centre for Research and Development

EMBO

Foundation for Polish Science

European Social Fund

National Science Centre

L’Oréal Poland

Polish Ministry of Science and Higher Education

European Regional Development Fund

University of Warsaw

Publisher

Oxford University Press (OUP)

Subject

Genetics

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