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A collection of gene deletions covering 96.5% of the genome was used to identify genes required for growth under various conditions, and to identify deletions resulting in aberrant cell shape.
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The first use of a highly innovative technique that automates genetic analysis in yeast is described. This was used to identify synthetic lethal interactions with mutations in genes involved in actin assembly, spindle orientation, and DNA synthesis.
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Tong A.H., Evangelista M., Parsons A.B., Xu H., Bader G.D., Page N., Robinson M., Raghibizadeh S., Hogue C.W., Bussey H.et al. Systematic genetic analysis with ordered arrays of yeast deletion mutants. Science. 294:2001;2364-2368 The first use of a highly innovative technique that automates genetic analysis in yeast is described. This was used to identify synthetic lethal interactions with mutations in genes involved in actin assembly, spindle orientation, and DNA synthesis.
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This study combines computational and experimental approaches to identify comprehensively protein-protein interactions for Src homology 3 (SH3)-domain-containing proteins in yeast. A highly interconnected interaction network was identified that could possibly be involved in regulating actin assembly.
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Tong A.H., Drees B., Nardelli G., Bader G.D., Brannetti B., Castagnoli L., Evangelista M., Ferracuti S., Nelson B., Paoluzi S.et al. A combined experimental and computational strategy to define protein interaction networks for peptide recognition modules. Science. 295:2002;321-324 This study combines computational and experimental approaches to identify comprehensively protein-protein interactions for Src homology 3 (SH3)-domain-containing proteins in yeast. A highly interconnected interaction network was identified that could possibly be involved in regulating actin assembly.
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Systematic two-hybrid screening was used to identify interacting partners of 54 proteins involved in cell polarity.
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An inhibitor-sensitive allele of Pho85 was used in combination with gene expression profiling to suggest a possible role for Pho85 in responding to diverse cellular stresses.
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Carroll A.S., Bishop A.C., DeRisi J.L., Shokat K.M., O'Shea E.K. Chemical inhibition of the Pho85 cyclin-dependent kinase reveals a role in the environmental stress response. Proc. Natl. Acad. Sci. U.S.A. 98:2001;12578-12583 An inhibitor-sensitive allele of Pho85 was used in combination with gene expression profiling to suggest a possible role for Pho85 in responding to diverse cellular stresses.
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27
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Dissection of a complex phenotype by functional genomics reveals roles for the yeast cyclin-dependent protein kinase Pho85 in stress adaptation and cell integrity
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A combination of synthetic genetic array (SGA) analysis and gene expression profiling was used to suggest a role for Pho85 in cell integrity. This is the first study to use SGA analysis to identify second-site suppressors.
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Huang D., Moffat J., Andrews B. Dissection of a complex phenotype by functional genomics reveals roles for the yeast cyclin-dependent protein kinase Pho85 in stress adaptation and cell integrity. Mol. Cell. Biol. 22:2002;5076-5088 A combination of synthetic genetic array (SGA) analysis and gene expression profiling was used to suggest a role for Pho85 in cell integrity. This is the first study to use SGA analysis to identify second-site suppressors.
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31
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0037131572
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This study demonstrates the usefulness of mass spectrometry in identifying components of protein complexes and specific phosphorylation sites within these complexes.
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Cheeseman I.M., Anderson S., Jwa M., Green E., Kang J., Yates J.R., Chan C.S.M., Drubin D., Barnes G. Phosphoregulation of kinetochore-microtubule attachments by the Aurora kinase Ipl1p. Cell. 111:2002;163-172 This study demonstrates the usefulness of mass spectrometry in identifying components of protein complexes and specific phosphorylation sites within these complexes.
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32
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This study demonstrates how systematic purification of protein complexes based on affinity to different subunits, in combination with statistical analysis, can be utilized to identify associated proteins.
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Sanders S.L., Jennings J., Canutescu A., Link A.J., Weil P.A. Proteomics of the eukaryotic transcription machinery: identification of proteins associated with components of yeast TFIID by multidimensional mass spectrometry. Mol. Cell. Biol. 22:2002;4723-4738 This study demonstrates how systematic purification of protein complexes based on affinity to different subunits, in combination with statistical analysis, can be utilized to identify associated proteins.
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Evidence that the Ipl1-Sli15 (Aurora kinase-INCENP) complex promotes chromosome bi-orientation by altering kinetochore-spindle pole connections
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Tanaka T.U., Rachidi N., Janke C., Pereira G., Galova M., Schiebel E., Stark M.J., Nasmyth K. Evidence that the Ipl1-Sli15 (Aurora kinase-INCENP) complex promotes chromosome bi-orientation by altering kinetochore-spindle pole connections. Cell. 108:2002;317-329.
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Shotgun identification of protein modifications from protein complexes and lens tissue
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MacCoss M.J., McDonald W.H., Saraf A., Sadygov R., Clark J.M., Tasto J.J., Gould K.L., Wolters D., Washburn M., Weiss A.et al. Shotgun identification of protein modifications from protein complexes and lens tissue. Proc. Natl. Acad. Sci. U.S.A. 99:2002;7900-7905.
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35
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Genomic analysis of homotypic vacuole fusion
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The gene deletion collection was used to identify proteins required for normal vacuolar morphology, identifying genes required for proper vacuole fusion.
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Seeley E.S., Kato M., Margolis N., Wickner W., Eitzen G. Genomic analysis of homotypic vacuole fusion. Mol. Biol. Cell. 13:2002;782-794 The gene deletion collection was used to identify proteins required for normal vacuolar morphology, identifying genes required for proper vacuole fusion.
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36
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0036320668
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The gene deletion collection was used to identify proteins required for proper sorting of a vacuole protein.
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Bonangelino C.J., Chavez E.M., Bonifacino J.S. Genomic screen for vacuolar protein sorting genes in Saccharomyces cerevisiae. Mol. Biol. Cell. 13:2002;2486-2501 The gene deletion collection was used to identify proteins required for proper sorting of a vacuole protein.
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Eitzen G., Wang L., Thorngren N., Wickner W. Remodeling of organelle-bound actin is required for yeast vacuole fusion. J. Cell. Biol. 158:2002;669-679.
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The gene deletion collection was used to identify proteins required for respiration and proper mitochondrial morphology.
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Dimmer K.S., Fritz S., Fuchs F., Messerschmitt M., weinbach N., Neupert W., Westermann B. Genetic basis of mitochondrial function and morphology in Saccharomyces cerevisiae. Mol. Cell. Biol. 13:2002;847-853 The gene deletion collection was used to identify proteins required for respiration and proper mitochondrial morphology.
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Dimmer, K.S.1
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39
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Giaever, G.1
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40
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