The broad, long-term objectives of this proposal are to determine at a molecular level, the mechanism of transcription initiation by RNA Polymerases II and III. These studies will lead to a better understanding of the transcription machinery and how it is regulated. This is important because the transcription machinery is the ultimate target of many signal transduction, cell cycle, and developmental pathways. Understanding the fundamental process of gene control will provide a basis for understanding many types of diseases such as cancer and syndromes involving DNA repair defects which can result from aberrant gene regulation, or from mutations in the transcription machinery.
The specific aims of this project are designed to study through molecular, biochemical and genetic methods, the mechanisms of transcription initiation and reinitiation utilized by RNA Polymerases II and III. The role of novel factors, which interact with the TFIIA terminal domain in preinitiation complexes (PICs), will be identified. The mechanism of Pol II transcription reinitiation will be investigated with a focus on the role of the mediator factor and identification of a form of Pol II used in the reinitiation reaction. The role of several distinct mediator complexes in gene regulation will be studied. The role of the core domain of the Pol III factor BRF will be elucidated, and compared to the role of the homologous region of the Pol II factor TFIIB. Finally, the target of the zinc ribbon domains in TFIIB and Brf will be identified, comparing the role of these domains in Pol II and III transcription.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM053451-09
Application #
6706256
Study Section
Cell Development and Function Integrated Review Group (CDF)
Program Officer
Tompkins, Laurie
Project Start
1995-09-30
Project End
2005-03-31
Budget Start
2004-04-01
Budget End
2005-03-31
Support Year
9
Fiscal Year
2004
Total Cost
$269,048
Indirect Cost
Name
Fred Hutchinson Cancer Research Center
Department
Type
DUNS #
078200995
City
Seattle
State
WA
Country
United States
Zip Code
98109
Donczew, Rafal; Hahn, Steven (2018) Mechanistic Differences in Transcription Initiation at TATA-Less and TATA-Containing Promoters. Mol Cell Biol 38:
Grünberg, Sebastian; Zentner, Gabriel E (2017) Genome-wide Mapping of Protein-DNA Interactions with ChEC-seq in Saccharomyces cerevisiae. J Vis Exp :
Grünberg, Sebastian; Zentner, Gabriel E (2017) Genome-wide characterization of Mediator recruitment, function, and regulation. Transcription 8:169-174
Warfield, Linda; Ramachandran, Srinivas; Baptista, Tiago et al. (2017) Transcription of Nearly All Yeast RNA Polymerase II-Transcribed Genes Is Dependent on Transcription Factor TFIID. Mol Cell 68:118-129.e5
Baptista, Tiago; Grünberg, Sebastian; Minoungou, Nadège et al. (2017) SAGA Is a General Cofactor for RNA Polymerase II Transcription. Mol Cell 68:130-143.e5
Tomko, Eric J; Fishburn, James; Hahn, Steven et al. (2017) TFIIH generates a six-base-pair open complex during RNAP II transcription initiation and start-site scanning. Nat Struct Mol Biol 24:1139-1145
Fishburn, James; Galburt, Eric; Hahn, Steven (2016) Transcription Start Site Scanning and the Requirement for ATP during Transcription Initiation by RNA Polymerase II. J Biol Chem 291:13040-7
Grünberg, Sebastian; Henikoff, Steven; Hahn, Steven et al. (2016) Mediator binding to UASs is broadly uncoupled from transcription and cooperative with TFIID recruitment to promoters. EMBO J 35:2435-2446
Warfield, Linda; Luo, Jie; Ranish, Jeffrey et al. (2016) Function of Conserved Topological Regions within the Saccharomyces cerevisiae Basal Transcription Factor TFIIH. Mol Cell Biol 36:2464-75
Fishburn, James; Tomko, Eric; Galburt, Eric et al. (2015) Double-stranded DNA translocase activity of transcription factor TFIIH and the mechanism of RNA polymerase II open complex formation. Proc Natl Acad Sci U S A 112:3961-6

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