The long-term goal of this study is to understand the biochemical mechanisms that underlie the regulation of eukaryotic mRNA synthesis. Specifically, the studies focus on understanding how the activity of the mammalian RNA polymerase II is controlled by transcription factors that direct initiation and elongation of transcripts from a large number of core promoters in vitro. The overall approach is to reconstitute with purified enzymes, faithful and efficient transcription in vitro, and to use this reconstituted system to elucidate the biochemical mechanisms governing transcription initiation and elongation by mammalian RNA polymerase II. The research will be organized along the following lines: (1) Detailed analysis of the mechanisms of action of novel RNA polymerase II elongation factors ELL and ELL2. (2) Further investigation of the mechanism of action of RNA polymerase II elongation factor Elongin. (3) Purification and characterization of RNA polymerase II elongation factor S-IV. (4) Detailed Investigation of the roles of TFIIE, TFIIF, TFIIH and ATP in transcription initiation and efficient promoter escape by RNA polymerase II. Additionally, studies are proposed to continue the studies on the functional relationship between the Elongin B and C regulatory subunits and the product of the VHL tumor suppressor gene.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
2R37GM041628-13
Application #
6129346
Study Section
Biochemistry Study Section (BIO)
Program Officer
Tompkins, Laurie
Project Start
1989-09-01
Project End
2001-06-30
Budget Start
2000-04-01
Budget End
2001-06-30
Support Year
13
Fiscal Year
2000
Total Cost
$387,600
Indirect Cost
Name
Oklahoma Medical Research Foundation
Department
Type
DUNS #
937727907
City
Oklahoma City
State
OK
Country
United States
Zip Code
73104
Sato, Shigeo; Tomomori-Sato, Chieri; Tsai, Kuang-Lei et al. (2016) Role for the MED21-MED7 Hinge in Assembly of the Mediator-RNA Polymerase II Holoenzyme. J Biol Chem 291:26886-26898
Sardiu, Mihaela E; Gilmore, Joshua M; Groppe, Brad D et al. (2015) Conserved abundance and topological features in chromatin-remodeling protein interaction networks. EMBO Rep 16:116-26
Takahashi, Hidehisa; Takigawa, Ichigaku; Watanabe, Masashi et al. (2015) MED26 regulates the transcription of snRNA genes through the recruitment of little elongation complex. Nat Commun 6:5941
Weems, Juston C; Slaughter, Brian D; Unruh, Jay R et al. (2015) Assembly of the Elongin A Ubiquitin Ligase Is Regulated by Genotoxic and Other Stresses. J Biol Chem 290:15030-41
Masuda, Yasushi; Takahashi, Hidehisa; Sato, Shigeo et al. (2015) TRIM29 regulates the assembly of DNA repair proteins into damaged chromatin. Nat Commun 6:7299
Chen, Lu; Ooi, Soon-Keat; Conaway, Ronald C et al. (2014) Generation and purification of human INO80 chromatin remodeling complexes and subcomplexes. J Vis Exp :e51720
Chen, Lu; Ooi, Soon-Keat; Conaway, Joan W et al. (2014) Biochemical assays for analyzing activities of ATP-dependent chromatin remodeling enzymes. J Vis Exp :e51721
Zhao, Xiaoming; Su, Jiaming; Wang, Fei et al. (2013) Crosstalk between NSL histone acetyltransferase and MLL/SET complexes: NSL complex functions in promoting histone H3K4 di-methylation activity by MLL/SET complexes. PLoS Genet 9:e1003940
Tomomori-Sato, Chieri; Sato, Shigeo; Conaway, Ronald C et al. (2013) Immunoaffinity purification of protein complexes from Mammalian cells. Methods Mol Biol 977:273-87
Sela, Dotan; Conkright, Juliana J; Chen, Lu et al. (2013) Role for human mediator subunit MED25 in recruitment of mediator to promoters by endoplasmic reticulum stress-responsive transcription factor ATF6?. J Biol Chem 288:26179-87

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