| Literature DB >> 35524108 |
Lieselotte Vermeersch1,2, Abbas Jariani1,2, Jana Helsen1,2,3, Benjamin M Heineike4,5,6, Kevin J Verstrepen7,8.
Abstract
Single-cell RNA sequencing (scRNA-seq) is emerging as an essential technique for studying the physiology of individual cells in populations. Although well-established and optimized for mammalian cells, research of microorganisms has been faced with major technical challenges for using scRNA-seq, because of their rigid cell wall, smaller cell size and overall lower total RNA content per cell. Here, we describe an easy-to-implement adaptation of the protocol for the yeast Saccharomyces cerevisiae using the 10× Genomics platform, originally optimized for mammalian cells. Introducing Zymolyase, a cell wall-digesting enzyme, to one of the initial steps of single-cell droplet formation allows efficient in-droplet lysis of yeast cells, without affecting the droplet emulsion and further sample processing. In addition, we also describe the downstream data analysis, which combines established scRNA-seq analysis protocols with specific adaptations for yeast, and R-scripts for further secondary analysis of the data.Entities:
Keywords: 10× Genomics; Saccharomyces cerevisiae; Single-cell RNA sequencing; Single-cell omics; Transcriptomics; Yeast
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Year: 2022 PMID: 35524108 DOI: 10.1007/978-1-0716-2257-5_1
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745