Information about most Saccharomyces cerevisiae genes, whether newly discovered or previously identified, is very limited. We have been using a transposon tagging strategy to analyze gene expression, protein localization, and gene disruption phenotypes for a large fraction of yeast genes with the ultimate goal of characterizing the yeast genome. Our transposons construct reporter gene fusions, epitope tag yeast proteins and large and small insertions in yeast genes. In the proposed funding period we plan to complete the collection of transposon insertions for every gene in the yeast genome. We will determine the subcellular localization of proteins by indirect immunofluorescence. Nuclear proteins will be analyzed to identify chromosomal proteins, and all of the binding targets of chromosomal proteins will be analyzed using a novel method involving chromatin immunoprecipitations and microarrays. We will generate a collection of yeast strains containing mutations in essential genes and attempt to characterize these strains using novel parallel screening methods and inducible protease cleavage methods. Finally, non-annotated reading frames and out- of frame coding sequences will be mutated and disruption phenotypes analyzed. We expect this project to have a significant impact on the scientific community. The information generated will be maintained in a database accessible by the Internet. Any researcher who identifies a yeast gene will be able to determine when the gene is expressed, the subcellular localization of the gene product and perhaps factors that regulate that gene's expression. Most importantly, plasmid alleles, libraries and yeast strains will be made available to all interested researchers. The technology proposed and the information gained will be applicable to the study of other organisms.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA077808-05
Application #
6376751
Study Section
Genome Study Section (GNM)
Program Officer
Felsenfeld, Adam
Project Start
1997-09-01
Project End
2005-07-31
Budget Start
2001-08-01
Budget End
2002-07-31
Support Year
5
Fiscal Year
2001
Total Cost
$711,407
Indirect Cost
Name
Yale University
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
06520
Gallagher, Jennifer E G; Zheng, Wei; Rong, Xiaoqing et al. (2014) Divergence in a master variator generates distinct phenotypes and transcriptional responses. Genes Dev 28:409-21
Waern, Karl; Snyder, Michael (2013) Extensive transcript diversity and novel upstream open reading frame regulation in yeast. G3 (Bethesda) 3:343-52
Zheng, Wei; Zhao, Hongyu; Mancera, Eugenio et al. (2010) Genetic analysis of variation in transcription factor binding in yeast. Nature 464:1187-91
Kasowski, Maya; Grubert, Fabian; Heffelfinger, Christopher et al. (2010) Variation in transcription factor binding among humans. Science 328:232-5
Snyder, Michael; Gallagher, Jennifer E G (2009) Systems biology from a yeast omics perspective. FEBS Lett 583:3895-9
Wang, Zhong; Gerstein, Mark; Snyder, Michael (2009) RNA-Seq: a revolutionary tool for transcriptomics. Nat Rev Genet 10:57-63
Nagalakshmi, Ugrappa; Wang, Zhong; Waern, Karl et al. (2008) The transcriptional landscape of the yeast genome defined by RNA sequencing. Science 320:1344-9
Hall, David A; Ptacek, Jason; Snyder, Michael (2007) Protein microarray technology. Mech Ageing Dev 128:161-7
Srikantha, Thyagarajan; Borneman, Anthony R; Daniels, Karla J et al. (2006) TOS9 regulates white-opaque switching in Candida albicans. Eukaryot Cell 5:1674-87
Seringhaus, Michael; Kumar, Anuj; Hartigan, John et al. (2006) Genomic analysis of insertion behavior and target specificity of mini-Tn7 and Tn3 transposons in Saccharomyces cerevisiae. Nucleic Acids Res 34:e57

Showing the most recent 10 out of 33 publications