Cited by 2,138Fungal and yeast genetics researchBioinformatics and Genomic NetworksGene Regulatory Network Analysis

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Systematic Genetic Analysis with Ordered Arrays of Yeast Deletion Mutants

Tong, Amy Hin Yan, Evangelista, Marie, Parsons, Ainslie B., Xu, Hong, Bader, Gary D., Pagé, Nicholas, Robinson, Mark, Raghibizadeh, Sasan, Hogue, Christopher W. V., Bussey, Howard, Andrews, Brenda, Tyers, Mike, Boone, Charles·2001·Science

DOI 10.1126/science.1065810

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Abstract

In Saccharomyces cerevisiae , more than 80% of the ∼6200 predicted genes are nonessential, implying that the genome is buffered from the phenotypic consequences of genetic perturbation. To evaluate function, we developed a method for systematic construction of double mutants, termed synthetic genetic array (SGA) analysis, in which a query mutation is crossed to an array of ∼4700 deletion mutants. Inviable double-mutant meiotic progeny identify functional relationships between genes. SGA analysis of genes with roles in cytoskeletal organization ( BNI1 , ARP2 , ARC40 , BIM1 ), DNA synthesis and repair ( SGS1 , RAD27 ), or uncharacterized functions ( BBC1 , NBP2 ) generated a network of 291 interactions among 204 genes. Systematic application of this approach should produce a global map of gene function.

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Functional Characterization of the S. cerevisiae Genome by Gene Deletion and Parallel Analysis
Winzeler, E. A., Shoemaker, D. D., Astromoff, A., Liang, H., Anderson, K., Andre, B., Bangham, R., Benito, R., Boeke, J. D., Bussey, H., et al. (1999) · Science · doi:10.1126/science.285.5429.901 · Cited by 3,953
Self-citation
BIND--The Biomolecular Interaction Network Database
Bader, G. D. (2001) · Nucleic Acids Research · doi:10.1093/nar/29.1.242 · Cited by 1,560
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Hartman, J. L., Garvik, B., & Hartwell, L. (2001) · Science · doi:10.1126/science.1056072 · Cited by 808
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Hartwell, L. H., Szankasi, P., Roberts, C. J., Murray, A. W., & Friend, S. H. (1997) · Science · doi:10.1126/science.278.5340.1064 · Cited by 789
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Evangelista, M., Blundell, K., Longtine, M. S., Chow, C. J., Adames, N. R., Pringle, J. R., Peter, M., & Boone, C. M. (1997) · Science · doi:10.1126/science.276.5309.118 · Cited by 647
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Quantitative phenotypic analysis of yeast deletion mutants using a highly parallel molecular bar–coding strategy
Shoemaker, D. D., Lashkari, D. A., Morris, D., Mittmann, M., & Davis, R. W. (1996) · Nature Genetics · doi:10.1038/ng1296-450 · Cited by 569
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Hughes, T. R., Roberts, C. J., Dai, H. A., Jones, A. R., Meyer, M. R., Slade, D., Burchard, J., Dow, S., Ward, T. R., Kidd, M. J., et al. (2000) · Nature Genetics · doi:10.1038/77116 · Cited by 482
Use of a screen for synthetic lethal and multicopy suppressee mutants to identify two new genes involved in morphogenesis in Saccharomyces cerevisiae.
Bender, A., & Pringle, J. R. (1991) · Molecular and Cellular Biology · doi:10.1128/mcb.11.3.1295 · Cited by 433
Robustness against mutations in genetic networks of yeast
Wagner, A. (2000) · Nature Genetics · doi:10.1038/74174 · Cited by 411
Requirement for Three Novel Protein Complexes in the Absence of the Sgs1 DNA Helicase in Saccharomyces cerevisiae
Mullen, J. R., Kaliraman, V., Ibrahim, S. S., & Brill, S. J. (2001) · Genetics · doi:10.1093/genetics/157.1.103 · Cited by 405

Show all 23 references

Research works printed but not linked: 4

Pringle J. R., Mol. Cell. Biol. 11, 1295 (1991).
I. Herskowitz J. Rine J. Strathern in The Molecular and Cellular Biology of the Yeast Saccharomyces cerevisiae vol. 2 Gene Expression E. W. Jones J. R. Pringle J. R. Broach Eds. (Cold Spring Harbor Laboratory Cold Spring Harbor NY 1992) pp. 583–656.
M. Evangelista et al. Nature Cell Biol. in press.
The following supplementary material is available on Science Online at www.sciencemag.org/cgi/content/full/294/5550/2364/DC1: supplementary table 1 a table of the deletion mutants used to create the double-mutant arrays shown in Fig. 2A by SGA analysis; supplementary table 2 a table of the 4672 unique deletion mutants assembled for large-scale SGA analysis; supplementary notes a description of the materials and methods for SGA analysis and bioinformatic analysis (yeast strains will be provided upon request); supplementary table 3 a table summarizing all the synthetic lethal/fitness interactions; supplementary table 4 a table of 523 gene deletions within the array that often appeared to be synthetically lethal with a wild-type control strain; supplementary table 5 a table of the overlap of the genetic interactions presented in Fig. 3 and the published genetic interactions assembled at MIPS (Munich Information Center for Protein Sequences) and YPD; supplementary fig. 1 a figure of the protein-protein interactions corresponding to genes within the genetic-interaction network shown in Fig. 3; supplementary table 6 a table of the gene deletions that are linked to the query gene and appeared to be synthetically lethal; supplementary fig. 2 a figure that shows two-dimensional clustering analysis of synthetic lethal interactions; supplementary table 7 a table that shows an analysis of the false-positives for the BIM1 and SGS1 screens as a comparison of the list of gene deletions that were scored as positive by SGA analysis to the list of gene deletions that were ultimately confirmed to be synthetically lethal by tetrad analysis; and supplementary table 8 a table of the synthetic genetic interactions and their BIND identification numbers.

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Cullen, P. J., & Sprague, G. F. (2002) · Eukaryotic Cell · doi:10.1128/ec.1.6.884-894.2002 · Cited by 33
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Authors: Tong, A. H. Y., Evangelista, M., Parsons, A. B., Xu, H., Bader, G. D., Pagé, N., Robinson, M., Raghibizadeh, S., Hogue, C. W. V., Bussey, H., Andrews, B., Tyers, M., & Boone, C.
Affiliations: University of Toronto (CA)
Queen's University (CA)
Mount Sinai Hospital (CA)
McGill University (CA)
Virtek Engineering Sciences, Inc. (VESI), 1 Bedford Road, Toronto ON, Canada M5R 2J7.
Corresponding author: Andrews, Brenda
Tyers, Mike
Boone, Charles
ORCID: Tong, Amy Hin Yan
Evangelista, Marie
Xu, Hong
Bader, Gary D.
Robinson, Mark
Hogue, Christopher W. V.
Andrews, Brenda
Tyers, Mike
Boone, Charles
Venue: Science
Publisher: American Association for the Advancement of Science (AAAS)
Published: 2001-12-14
Volume: 294
Issue: 5550
Pages: 2364-2368
ISSN: 0036-8075 (ISSN-L)
1095-9203
DOI: 10.1126/science.1065810
OpenAlex: W2127073167
Cited by: 2,138
References: 23
Citations by year: 2026: 24 · 2025: 39 · 2024: 51 · 2023: 51 · 2022: 49 · 2021: 67 · 2020: 71 · 2019: 63 · 2018: 65 · 2017: 105 · 2016: 73 · 2015: 96 · 2014: 115 · 2013: 101 · 2012: 107
FWCI: 27.25
Type: journal article
Language: en
Open access: closed
Locations: Science (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gene Regulatory Network Analysis
Keywords: synthetic genetic array, yeast deletion mutants, genetic interactions, cytoskeletal organization, non-essential genes, Saccharomyces cerevisiae
MeSH terms: Carrier Proteins, Crosses, Genetic, Cytoskeletal Proteins, Cytoskeleton, DNA Repair, DNA Helicases, DNA, Fungal, Endodeoxyribonucleases, Fungal Proteins, Genes, Fungal, Genetic Markers, Genetic Techniques, Microfilament Proteins, Microtubule Proteins, Mitosis, Recombination, Genetic, Robotics, Saccharomyces cerevisiae, Genome, Fungal, Cell Polarity, Gene Deletion, Cell Cycle Proteins, Computational Biology, Genes, Essential, Saccharomyces cerevisiae Proteins, Databases, Genetic, Flap Endonucleases, RecQ Helicases

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Systematic Genetic Analysis with Ordered Arrays of Yeast Deletion Mutants

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