| Literature DB >> 29043651 |
Hendrikje Göttert1,2, Mojca Mattiazzi Usaj1, Adam P Rosebrock1,2,3, Brenda J Andrews4,5.
Abstract
Fluorescent reporter genes have long been used to quantify various cell features such as transcript and protein abundance. Here, we describe a method, reporter synthetic genetic array (R-SGA) analysis, which allows for the simultaneous quantification of any fluorescent protein readout in thousands of yeast strains using an automated pipeline. R-SGA combines a fluorescent reporter system with standard SGA analysis and can be used to examine any array-based strain collection available to the yeast community. This protocol describes the R-SGA methodology for screening different arrays of yeast mutants including the deletion collection, a collection of temperature-sensitive strains for the assessment of essential yeast genes and a collection of inducible overexpression strains. We also present an alternative pipeline for the analysis of R-SGA output strains using flow cytometry of cells in liquid culture. Data normalization for both pipelines is discussed.Entities:
Keywords: Fluorescent protein; Reporter gene; SGA; Synthetic genetic array; Yeast
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Year: 2018 PMID: 29043651 DOI: 10.1007/978-1-4939-7306-4_40
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745