A long range goal is to be able to detail the events that occur during the initiation of transcription of protein coding genes (transcribed by the RNA polymerase II machinery and also called class II genes) through the characterization of the proteins involved and their various protein-DNA and protein-protein interactions with the intent of formulating a general mechanism for the initiation of transcription of class II genes. To this end, the overall aim of this proposal is to continue and expand studies now in progress in my laboratory on the general protein factors that are required for the transcription of Class II genes and to elucidate some of the mechanisms that modulate transcriptional expression of these genes.
The specific aims will be a detailed study of the reactions catalyzed by the general transcription factors required for transcription. These include studies on the interaction between the transcription factors, RNA polymerase II and promoter sequences through the use of techniques such as glycerol gradient centrifugation, gel filtration and protein cross linking. DNA footprinting will be used to analyze the DNA-protein interactions. Also, reagents that inhibit the transcription reaction at different stages (Sarkosyl or Heparin) will be used to define the steps at which each of the transcription factors act. I hope to be able to precisely define the order of interaction of the general transcription factors with each other and with the promoter sequences. These studies should yield basic models(s) from which the specific regulatory mechanisms of class II gene expression can be discerned at the molecular level.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM037120-04
Application #
3292144
Study Section
Molecular Biology Study Section (MBY)
Project Start
1986-11-01
Project End
1989-06-30
Budget Start
1988-07-01
Budget End
1989-06-30
Support Year
4
Fiscal Year
1988
Total Cost
Indirect Cost
Name
University of Medicine & Dentistry of NJ
Department
Type
Schools of Medicine
DUNS #
622146454
City
Piscataway
State
NJ
Country
United States
Zip Code
08854
Lecona, Emilio; Narendra, Varun; Reinberg, Danny (2015) USP7 cooperates with SCML2 to regulate the activity of PRC1. Mol Cell Biol 35:1157-68
Campos, Eric I; Smits, Arne H; Kang, Young-Hoon et al. (2015) Analysis of the Histone H3.1 Interactome: A Suitable Chaperone for the Right Event. Mol Cell 60:697-709
Tee, Wee-Wei; Shen, Steven S; Oksuz, Ozgur et al. (2014) Erk1/2 activity promotes chromatin features and RNAPII phosphorylation at developmental promoters in mouse ESCs. Cell 156:678-90
Lecona, Emilio; Rojas, Luis Alejandro; Bonasio, Roberto et al. (2013) Polycomb protein SCML2 regulates the cell cycle by binding and modulating CDK/CYCLIN/p21 complexes. PLoS Biol 11:e1001737
Beck, David B; Oda, Hisanobu; Shen, Steven S et al. (2012) PR-Set7 and H4K20me1: at the crossroads of genome integrity, cell cycle, chromosome condensation, and transcription. Genes Dev 26:325-37
Fuda, Nicholas J; Buckley, Martin S; Wei, Wenxiang et al. (2012) Fcp1 dephosphorylation of the RNA polymerase II C-terminal domain is required for efficient transcription of heat shock genes. Mol Cell Biol 32:3428-37
Mallen-St Clair, Jon; Soydaner-Azeloglu, Rengin; Lee, Kyoung Eun et al. (2012) EZH2 couples pancreatic regeneration to neoplastic progression. Genes Dev 26:439-44
Sims 3rd, Robert J; Rojas, Luis Alejandro; Beck, David B et al. (2011) The C-terminal domain of RNA polymerase II is modified by site-specific methylation. Science 332:99-103
Bonasio, Roberto; Tu, Shengjiang; Reinberg, Danny (2010) Molecular signals of epigenetic states. Science 330:612-6
Margueron, Raphael; Justin, Neil; Ohno, Katsuhito et al. (2009) Role of the polycomb protein EED in the propagation of repressive histone marks. Nature 461:762-7

Showing the most recent 10 out of 92 publications