| Literature DB >> 18622398 |
Zhun Yan1, Michael Costanzo, Lawrence E Heisler, Jadine Paw, Fiona Kaper, Brenda J Andrews, Charles Boone, Guri Giaever, Corey Nislow.
Abstract
The ability to perform complex bioassays in parallel enables experiments that are otherwise impossible because of throughput and cost constraints. For example, highly parallel chemical-genetic screens using pooled collections of thousands of defined Saccharomyces cerevisiae gene deletion strains are feasible because each strain is bar-coded with unique DNA sequences. It is, however, time-consuming and expensive to individually bar-code individual strains. To provide a simple and general method of barcoding yeast collections, we built a set of donor strains, called Barcoders, with unique bar codes that can be systematically transferred to any S. cerevisiae collection. We applied this technology by generating a collection of bar-coded 'decreased abundance by mRNA perturbation' (DAmP) loss-of-function strains comprising 87.1% of all essential yeast genes. These experiments validate both the Barcoders and the DAmP strain collection as useful tools for genome-wide chemical-genetic assays.Entities:
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Year: 2008 PMID: 18622398 DOI: 10.1038/nmeth.1231
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547