Control of gene expression is fundamental to life and this control usually involves transcriptional regulation. Much of the research on transcriptional regulation in eukaryotes over the past 2 decades has focused on regulatory mechanisms that ultimately affect transcription initiation by Pol II at protein-encoding genes. However, recent analyses of Pol II interactions in vivo using genome-wide mapping techniques such as ChIP- chip reveal that thousands of genes in human and Drosophila have Pol II concentrated at the 5'end. Much of this Pol II appears to have initiated transcription but paused in the promoter proximal region. Hence, a prominent control point in the transcription occurs after transcription initiation. This promoter proximal pausing and its regulation are poorly understood largely because it has gone unrecognized at most genes. The hsp70 gene of Drosophila is one of the few genes where promoter proximal pausing has long been known to occur, and it serves a paradigm for this process. The sequence-specific, DNA-binding proteins, GAGA factor and HSF, function respectively in the establishment and reactivation of the paused Pol II. The negative elongation factors, NELF and DSIF, participate in pausing by associating with Pol II. The positive elongation factor, P- TEFb, is thought to reactivate the paused Pol II by phosphorylating NELF, DSIF and Pol II. Even with the identification of these proteins, the mechanisms by which they control the Pol II are not known. The overall goal of this project is to elucidate mechanisms of promoter proximal pausing and its control.
Aim 1 determines how DSIF and NELF cause Pol II to pause and how their activities are regulated by post-translational modifications.
Aim 2 determines how GAGA factor and HSF control promoter proximal pausing. It also investigates the role of a novel sequence-specific, DNA-binding protein whose DNA binding site is detected in at the promoter of 20% of genes found to be associated with Pol II.
Aim 3 will determine if the regulation of promoter proximal pausing involves kinetic competition between the rate of elongation and the rate at which DSIF and NELF capture the elongating Pol II. A combination of biochemical and in vivo approaches applied to the model organism, Drosophila, uniquely qualifies this project for obtaining significant insight into the mechanism of promoter proximal pausing, thereby having significant impact our fundamental understanding of gene regulation. In addition, NELF, DSIF and P-TEFb have each been linked to human maladies. One subunit of NELF associates with the BRCA1 and has been linked to breast cancer. DSIF and P-TEFb both contribute to transcription of the HIV provirus, and an inhibitor of P-TEFb is in phase 2 clinical trials for cancer therapy.

Public Health Relevance

Transcriptional regulation plays a prominent role in the appropriate expression of genes, and many diseases arise because of defects in gene expression. Recent research has revealed that a mechanism of transcriptional regulation called promoter proximal pausing, once thought to occur at only a handful of genes, actually happens at thousands of genes including ones involved in development and stem cell renewal. Promoter proximal pausing will be studied in the model organism, Drosophila, which offers a unique combination of experimental approaches for understanding this important biological process.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
3R01GM047477-20S1
Application #
8845915
Study Section
Molecular Genetics B Study Section (MGB)
Program Officer
Sledjeski, Darren D
Project Start
1992-05-01
Project End
2015-04-30
Budget Start
2013-03-01
Budget End
2015-04-30
Support Year
20
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Pennsylvania State University
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
City
University Park
State
PA
Country
United States
Zip Code
16802
Qiu, Yijun; Gilmour, David S (2017) Identification of Regions in the Spt5 Subunit of DRB Sensitivity-inducing Factor (DSIF) That Are Involved in Promoter-proximal Pausing. J Biol Chem 292:5555-5570
Mayfield, Joshua E; Robinson, Michelle R; Cotham, Victoria C et al. (2017) Mapping the Phosphorylation Pattern of Drosophila melanogaster RNA Polymerase II Carboxyl-Terminal Domain Using Ultraviolet Photodissociation Mass Spectrometry. ACS Chem Biol 12:153-162
Baumann, Douglas G; Gilmour, David S (2017) A sequence-specific core promoter-binding transcription factor recruits TRF2 to coordinately transcribe ribosomal protein genes. Nucleic Acids Res 45:10481-10491
Gibbs, Eric B; Lu, Feiyue; Portz, Bede et al. (2017) Phosphorylation induces sequence-specific conformational switches in the RNA polymerase II C-terminal domain. Nat Commun 8:15233
Portz, Bede; Lu, Feiyue; Gibbs, Eric B et al. (2017) Structural heterogeneity in the intrinsically disordered RNA polymerase II C-terminal domain. Nat Commun 8:15231
Baumann, Douglas G; Dai, Mu-Shui; Lu, Hua et al. (2017) GFZF, a glutathione S-transferase protein implicated in cell cycle regulation and hybrid inviability, is a transcriptional co-activator. Mol Cell Biol :
Li, Jian; Gilmour, David S (2015) Reconstitution of factor-dependent, promoter proximal pausing in Drosophila nuclear extracts. Methods Mol Biol 1276:133-52
Achary, Bhavana G; Campbell, Katie M; Co, Ivy S et al. (2014) RNAi screen in Drosophila larvae identifies histone deacetylase 3 as a positive regulator of the hsp70 heat shock gene expression during heat shock. Biochim Biophys Acta 1839:355-63
Li, Jian; Gilmour, David S (2013) Distinct mechanisms of transcriptional pausing orchestrated by GAGA factor and M1BP, a novel transcription factor. EMBO J 32:1829-41
Li, Jian; Liu, Yingyun; Rhee, Ho Sung et al. (2013) Kinetic competition between elongation rate and binding of NELF controls promoter-proximal pausing. Mol Cell 50:711-22

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