Eukaryotic cell cycles seem to be controlled by a mysterious """"""""commitment"""""""" event. In the yeast Saccharomyces cerevisiae, genes affecting the commitment event have been identified. Some of these genes, the Start genes, are required for commitment to occur, and other genes, the Whi genes, help determine when commitment will occur. The behaviour of at least one of the Whi mutants is consistent with the idea that the concentration of the gene product changes through the cell cycle, and at a critical concentration, commitment to a new cycle, and at a critical concentration, commitment to a new cell cycle is triggered. That is, the Whi gene product may be the metric that directly triggers commitment.
The aim of this project is to characterize the Whi genes at the molecular level. Presently known Whi genes will be cloned, sequenced, mutated, and otherwise characterized. New Whi genes and interacting genes will be identified, and similarly characterized. Physiological studies of Whi mutants and some Start mutants will be undertaken, and the Whi gene products will be characterized biochemically, in an effort to determine the molecular nature of the commitment event. Through suppressor studies, an attempt will be made to identify Start genes that directly interact with Whi genes. Other eukaryotes will be screened for proteins antigenically related to the Whi proteins, in order to determine how generally applicable the mechanisms of yeast cell cycle control may be.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
1R01GM039978-01
Application #
3297276
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1988-04-01
Project End
1993-03-31
Budget Start
1988-04-01
Budget End
1989-03-31
Support Year
1
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Cold Spring Harbor Laboratory
Department
Type
DUNS #
065968786
City
Cold Spring Harbor
State
NY
Country
United States
Zip Code
11724
Gao, Shujuan; Honey, Sangeet; Futcher, Bruce et al. (2016) The non-homologous end-joining pathway of S. cerevisiae works effectively in G1-phase cells, and religates cognate ends correctly and non-randomly. DNA Repair (Amst) 42:1-10
Zhao, Gang; Chen, Yuping; Carey, Lucas et al. (2016) Cyclin-Dependent Kinase Co-Ordinates Carbohydrate Metabolism and Cell Cycle in S. cerevisiae. Mol Cell 62:546-57
Garg, Angad; Futcher, Bruce; Leatherwood, Janet (2015) A new transcription factor for mitosis: in Schizosaccharomyces pombe, the RFX transcription factor Sak1 works with forkhead factors to regulate mitotic expression. Nucleic Acids Res 43:6874-88
Cai, Ying; Futcher, Bruce (2013) Effects of the yeast RNA-binding protein Whi3 on the half-life and abundance of CLN3 mRNA and other targets. PLoS One 8:e84630
Ferrezuelo, Francisco; Colomina, Neus; Futcher, Bruce et al. (2010) The transcriptional network activated by Cln3 cyclin at the G1-to-S transition of the yeast cell cycle. Genome Biol 11:R67
Di Talia, Stefano; Wang, Hongyin; Skotheim, Jan M et al. (2009) Daughter-specific transcription factors regulate cell size control in budding yeast. PLoS Biol 7:e1000221
Wang, Hongyin; Carey, Lucas B; Cai, Ying et al. (2009) Recruitment of Cln3 cyclin to promoters controls cell cycle entry via histone deacetylase and other targets. PLoS Biol 7:e1000189
Honey, Sangeet; Futcher, Bruce (2007) Roles of the CDK phosphorylation sites of yeast Cdc6 in chromatin binding and rereplication. Mol Biol Cell 18:1324-36
Jorgensen, Paul; Edgington, Nicholas P; Schneider, Brandt L et al. (2007) The size of the nucleus increases as yeast cells grow. Mol Biol Cell 18:3523-32
Futcher, Bruce (2006) Metabolic cycle, cell cycle, and the finishing kick to Start. Genome Biol 7:107

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