Studies of animal tumor viruses such as SV40 have elucidated numerous mechanisms of both viral and cellular gene regulation. The first eukaryotic sequence-specific DNA binding protein to be isolated and characterized was the SV40 large T-ag. Early work on the SV40 T-ag revealed its remarkable multifunctional nature by its ability to mediate DNA replication, transcription and neoplastic tranformation. The studies of T-ag continue today with the recent high resolution X-ray structure of the T-ag dodecamer/ATPase which is responsible for DNA binding and initiation of viral DNA synthesis. The critical functions of the SV40 T-ag in controlling early viral and cellular gene regulation prompted our lab to launch a systematic analysis of the cellular machinery that works in conjunction with this viral trans-regulator to direct gene expression in animal cells. These studies have led to the discovery and biochemical characterization of over 75 transcription factors including sequence-specific enhancer/promoter recognition factors; core promoter/basal components of the pre-initiation RNA polymerase II complex; multi-subunit co-activators and chromatin remodeling co-factors. These biochemical studies have been combined with cell-based assays and gene targeting in the mouse to reveal an elaborate machinery which includes: cell-type specific and gene selective subunits of the core promoter recognition complex. In this grant renewal, we propose to continue our efforts to dissect the mechanisms by which the transcriptional apparatus operates to regulate gene expression in metazoan organisms. We will extend our effort to establish a highly purified in vitro transcription system using chromatinized DNA templates, focusing on uncovering the mechanisms of cell-type specific components of the core transcriptional machinery (i.e.TAFII105, TRF2, etc.). In addition to studying activation, we will renew our effort to study how viral and cellular proteins function in repression. Unlike previous grants, a significantly greater proportion of our work will be conducted in vivo (i.e. KO mice, immunofluorescence, FISH etc.). Finally, we will increase our effort in the area of structural analysis incorporating electron microscopy and single particle 3D reconstruction with X-ray crystallography to solve the 3D structure of large multi-subunit protein complexes. These studies should provide us with a comprehensive picture of how both viral and cellular genomes are expressed in a regulated fashion by the highly diversified transcriptional apparatus that has evolved in animal cells. Understanding the gene regulatory machinery has already provided the basis for developing various novel anti-cancer therapeutic strategies and we anticipate that as new target molecules are identified on the critical path leading to oncogenesis and disease, additional therapeutic interventions designed to intercede with gene regulatory mechanisms will emerge.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
2R37CA025417-27
Application #
6774187
Study Section
Virology Study Section (VR)
Program Officer
Blair, Donald G
Project Start
1979-04-01
Project End
2010-01-31
Budget Start
2005-02-01
Budget End
2006-01-31
Support Year
27
Fiscal Year
2005
Total Cost
$545,795
Indirect Cost
Name
University of California Berkeley
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
124726725
City
Berkeley
State
CA
Country
United States
Zip Code
94704
Levine, Michael; Cattoglio, Claudia; Tjian, Robert (2014) Looping back to leap forward: transcription enters a new era. Cell 157:13-25
Zhou, Haiying; Kaplan, Tommy; Li, Yan et al. (2013) Dual functions of TAF7L in adipocyte differentiation. Elife 2:e00170
Guglielmi, Benjamin; La Rochelle, Natalie; Tjian, Robert (2013) Gene-specific transcriptional mechanisms at the histone gene cluster revealed by single-cell imaging. Mol Cell 51:480-92
Fong, Yick W; Cattoglio, Claudia; Tjian, Robert (2013) The intertwined roles of transcription and repair proteins. Mol Cell 52:291-302
Revyakin, Andrey; Zhang, Zhengjian; Coleman, Robert A et al. (2012) Transcription initiation by human RNA polymerase II visualized at single-molecule resolution. Genes Dev 26:1691-702
Fong, Yick W; Cattoglio, Claudia; Yamaguchi, Teppei et al. (2012) Transcriptional regulation by coactivators in embryonic stem cells. Trends Cell Biol 22:292-8
Yao, Jie; Fetter, Richard D; Hu, Ping et al. (2011) Subnuclear segregation of genes and core promoter factors in myogenesis. Genes Dev 25:569-80
D'Alessio, Joseph A; Ng, Raymond; Willenbring, Holger et al. (2011) Core promoter recognition complex changes accompany liver development. Proc Natl Acad Sci U S A 108:3906-11
Liu, Zhe; Scannell, Devin R; Eisen, Michael B et al. (2011) Control of embryonic stem cell lineage commitment by core promoter factor, TAF3. Cell 146:720-31
Fong, Yick W; Inouye, Carla; Yamaguchi, Teppei et al. (2011) A DNA repair complex functions as an Oct4/Sox2 coactivator in embryonic stem cells. Cell 147:120-31

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