The long-term goal is to understand how prolyl-isomerases (PPIases) control important cellular processes such as transcription and mitosis. These enzymes catalyze the cis/trans isomerization of the peptide bond that precedes the cyclic amino acid proline. This conformational change is thought to be important for proper folding of proteins and control of their activity. PPIases are found in all organisms, and are best known because they are the targets of immunosuppressive and antifungal drugs. However, their normal function in cells is not understood, since most can be removed by gene deletion in their respective organism without observable consequences. There is one exception, however, a PPIase called Ess 1 that is required for growth in the yeast, Saccharomyces cerevisiae. Ess 1 and its human homolog, Pin 1, are implicated in cell cycle confrol. Recent discoveries show that Ess 1 interacts physically and genetically with the carboxy-terminal domain (CTD) of RNA polymerase II, suggesting a role in transcription of cell cycle genes. This study will take advantage of the essential nature of Ess 1 and the power of yeast genetics to elucidate the Ess1 pathway. The main focus will be to understand the role of Essi in transcription. Specifically, the aims are: (1) to define genetic interactions between the ESS1 gene and genes that are known to be important for transcription, (2) to discover genes whose transcription depends on Ess1 and that control cell cycle progression through mitosis, (3) to combine the use of yeast genetics with biochemistry to study how Ess1 binds the CTD, with the goal of determining how Ess1 controls RNA polymerase II function, and finally, (4) to examine the importance of Ess1 for virulence in pathogenic fungi, with the eventual goal of developing antifungal drugs that inhibit Ess1 function.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM055108-06
Application #
6519785
Study Section
Cell Development and Function Integrated Review Group (CDF)
Program Officer
Tompkins, Laurie
Project Start
1997-07-01
Project End
2005-06-30
Budget Start
2002-07-01
Budget End
2003-06-30
Support Year
6
Fiscal Year
2002
Total Cost
$219,459
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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