High-throughput classification of yeast mutants for functional genomics using metabolic footprinting
Created by W.Langdon from
gp-bibliography.bib Revision:1.7964
- @Article{Allen:2003:NB,
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author = "Jess Allen and Hazel M. Davey and David Broadhurst and
Jim K. Heald and Jem J. Rowland and
Stephen G. Oliver and Douglas B. Kell",
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title = "High-throughput classification of yeast mutants for
functional genomics using metabolic footprinting",
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journal = "Nature Biotechnology",
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year = "2003",
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volume = "21",
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number = "6",
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pages = "692--696",
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month = jun,
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email = "dbk@umist.ac.uk",
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keywords = "genetic algorithms, genetic programming",
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URL = "http://dbkgroup.org/Papers/NatureBiotechnology21(692-696).pdf",
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DOI = "doi:10.1038/nbt823",
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abstract = "Many technologies have been developed to help explain
the function of genes discovered by systematic genome
sequencing. At present, transcriptome and proteome
studies dominate large-scale functional analysis
strategies. Yet the metabolome, because it is
'downstream', should show greater effects of genetic or
physiological changes and thus should be much closer to
the phenotype of the organism. We earlier presented a
functional analysis strategy that used metabolic
fingerprinting to reveal the phenotype of silent
mutations of yeast genes1. However, this is difficult
to scale up for high-throughput screening. Here we
present an alternative that has the required throughput
(2 min per sample). This 'metabolic footprinting'
approach recognizes the significance of 'overflow
metabolism' in appropriate media. Measuring
intracellular metabolites is time-consuming and subject
to technical difficulties caused by the rapid turnover
of intracellular metabolites and the need to quench
metabolism and separate metabolites from the
extracellular space. We therefore focused instead on
direct, noninvasive, mass spectrometric monitoring of
extracellular metabolites in spent culture medium.
Metabolic footprinting can distinguish between
different physiological states of wild-type yeast and
between yeast single-gene deletion mutants even from
related areas of metabolism. By using appropriate
clustering and machine learning techniques, the latter
based on genetic programming2-8, we show that metabolic
footprinting is an effective method to classify
'unknown' mutants by genetic defect.",
- }
Genetic Programming entries for
Jess Allen
Hazel M Davey
David I Broadhurst
Jim K Heald
Jem J Rowland
Stephen G Oliver
Douglas B Kell
Citations