Yeast and human cells require the ESS1 gene in order to divide. This essential gene controls cell cycle progression through mitosis, and given its extraordinary conservation, is probably required in all eukaryotes. The goal of this work is to understand how ESS1 controls the cell cycle. The yeast saccharomyces cerevisiae, the organism in which ESS1 was discovered, will be used as a model system. ESS1 is highly conserved both structurally and functionally; ESS1 homologs from Drosophila melanogaster and humans rescue yeast ess1 mutants. The Ess1 protein and its counterparts are the only known proteins to contain both a WW domain and a PPIase (peptidyl-prolyl isomerase) domain. The WW domain is a protein-protein interaction module found in proteins such as Dystrophin, encoded by the human muscular dystrophy gene. The PPIase domain is a catalytic module that controls the folding and activity of kinases, receptors and transcription factors and is found in proteins like cyclophilin that mediate the effects of immunosuppressive drugs. How these domains function in Ess1 to control the cell cycle is not known. In this proposal, yeast genetics will be used understand how Ess1 controls mitotic progression and how the WW and PPIase domains contribute to this activity. This will be accomplished by (1) conducting an extensive structure- function analysis of the Ess1 WW and PPIase domains, (2) by isolating conditional alleles of ESS1 gene and using these alleles for cell cycle analysis, and (3) by identifying other components of the ESS1 pathway using suppressor screens and tow-hybrid selections. An understanding of how ESS1 functions in yeast will illuminate poorly understood pathways of mitotic regulation and will provide insight into the control of the cell cycle in all eukaryotic cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM055108-03
Application #
6019230
Study Section
Cellular Biology and Physiology Subcommittee 1 (CBY)
Project Start
1997-07-01
Project End
2001-06-30
Budget Start
1999-07-01
Budget End
2000-06-30
Support Year
3
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Wadsworth Center
Department
Type
DUNS #
110521739
City
Menands
State
NY
Country
United States
Zip Code
12204
Hanes, Steven D (2015) Prolyl isomerases in gene transcription. Biochim Biophys Acta 1850:2017-34
Allepuz-Fuster, Paula; Martínez-Fernández, Verónica; Garrido-Godino, Ana I et al. (2014) Rpb4/7 facilitates RNA polymerase II CTD dephosphorylation. Nucleic Acids Res 42:13674-88
Atencio, David; Barnes, Cassandra; Duncan, Thomas M et al. (2014) The yeast Ess1 prolyl isomerase controls Swi6 and Whi5 nuclear localization. G3 (Bethesda) 4:523-37
Hanes, Steven D (2014) The Ess1 prolyl isomerase: traffic cop of the RNA polymerase II transcription cycle. Biochim Biophys Acta 1839:316-33
Samaranayake, Dhanushki; Atencio, David; Morse, Randall et al. (2013) Role of Ess1 in growth, morphogenetic switching, and RNA polymerase II transcription in Candida albicans. PLoS One 8:e59094
Ma, Zhuo; Atencio, David; Barnes, Cassandra et al. (2012) Multiple roles for the Ess1 prolyl isomerase in the RNA polymerase II transcription cycle. Mol Cell Biol 32:3594-607
Cosgrove, Michael S; Ding, Ye; Rennie, William A et al. (2012) The Bin3 RNA methyltransferase targets 7SK RNA to control transcription and translation. Wiley Interdiscip Rev RNA 3:633-47
Samaranayake, Dhanushki P; Hanes, Steven D (2011) Milestones in Candida albicans gene manipulation. Fungal Genet Biol 48:858-65
McNaughton, Lynn; Li, Zhong; Van Roey, Patrick et al. (2010) Restricted domain mobility in the Candida albicans Ess1 prolyl isomerase. Biochim Biophys Acta 1804:1537-41
Singh, Navjot; Ma, Zhuo; Gemmill, Trent et al. (2009) The Ess1 prolyl isomerase is required for transcription termination of small noncoding RNAs via the Nrd1 pathway. Mol Cell 36:255-66

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