Our long term goal is to understand the molecular mechanisms of regulation of eukaryotic mRNA gene transcription. A comprehensive knowledge of transcriptional regulatory mechanisms is absolutely essential if we are to understand normal and pathological biological processes and conditions. Our studies utilize Bakers Yeast, Saccharomyces cerevisiae, as a model system for elucidating the detailed role that factor TFIID plays in the complicated process of mRNA gene transcription by RNA polymerase II. These studies are an outgrowth of our recent work on TBP the TATA-box Binding Protein, which we currently know is a subunit of at least two distinct RNA Polymerase II-specific multiprotein complexes: (1) it comprises the DNA- binding subunit of TFIID and (2) a complex containing at least one additional protein termed TAF170, TBP Associated Factor of Mr about 170,000. Work from a large number of different investigators has demonstrated that the multisubunit, TBP-containing TFIID complex is intimately involved in the regulatory events which actually control mRNA gene transcription. Hence, understanding the composition and function of TFIID/TBP and other TBP-containing complexes is key to knowing how gene transcription is controlled. The approach which we will be used i our experiments will be multi-faceted combining biochemical and genetic analyses focusing upon yeast TBP and the genes encoding the multiple yeast TAFs which we have recently cloned. We will examine the interplay of these factors with TBP, each other, promoter DNA, and RNA polymerase II. Successful completion of these experiments will greatly increase our understanding of the key process of RNA polymerase II transcription.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
1R01GM052461-01
Application #
2191495
Study Section
Molecular Cytology Study Section (CTY)
Project Start
1995-04-01
Project End
1999-03-31
Budget Start
1995-04-01
Budget End
1996-03-31
Support Year
1
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Physiology
Type
Schools of Medicine
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37212
Koster, Maria J E; Yildirim, Asli D; Weil, P Anthony et al. (2014) Suppression of intragenic transcription requires the MOT1 and NC2 regulators of TATA-binding protein. Nucleic Acids Res 42:4220-9
Layer, Justin H; Weil, P Anthony (2013) Direct TFIIA-TFIID protein contacts drive budding yeast ribosomal protein gene transcription. J Biol Chem 288:23273-94
Papai, Gabor; Weil, P Anthony; Schultz, Patrick (2011) New insights into the function of transcription factor TFIID from recent structural studies. Curr Opin Genet Dev 21:219-24
Layer, Justin H; Miller, Scott G; Weil, P Anthony (2010) Direct transactivator-transcription factor IID (TFIID) contacts drive yeast ribosomal protein gene transcription. J Biol Chem 285:15489-99
Papai, Gabor; Tripathi, Manish K; Ruhlmann, Christine et al. (2010) TFIIA and the transactivator Rap1 cooperate to commit TFIID for transcription initiation. Nature 465:956-60
Papai, Gabor; Tripathi, Manish K; Ruhlmann, Christine et al. (2009) Mapping the initiator binding Taf2 subunit in the structure of hydrated yeast TFIID. Structure 17:363-73
Bendjennat, Mourad; Weil, P Anthony (2008) The transcriptional repressor activator protein Rap1p is a direct regulator of TATA-binding protein. J Biol Chem 283:8699-710
Garbett, Krassimira A; Tripathi, Manish K; Cencki, Belgin et al. (2007) Yeast TFIID serves as a coactivator for Rap1p by direct protein-protein interaction. Mol Cell Biol 27:297-311
Powell, David W; Weaver, Connie M; Jennings, Jennifer L et al. (2004) Cluster analysis of mass spectrometry data reveals a novel component of SAGA. Mol Cell Biol 24:7249-59
Singh, Madhu V; Bland, Christin E; Weil, P Anthony (2004) Molecular and genetic characterization of a Taf1p domain essential for yeast TFIID assembly. Mol Cell Biol 24:4929-42

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