Transcriptional regulation is orchestrated by numerous positively and negatively acting factors that ensure proper temporal and spatial gene expression, vital for the development, health and viability of organisms. To date, biochemical and genetic studies have identified many of these factors and have provided mechanistic insights as to how they function to coordinate gene regulation. However, most of these studies, which require fixation of chromatin, only provide a static """"""""snap-shot"""""""" of the critical features of promoter architecture and mechanisms of regulation. However, more recent advances in optical technology allow for the real time imaging of transcription factors at loci in living cells. Recent studies from the Lis lab have utilized live cell imaging to study the dynamics and localization of Poll II at the HS loci in living cells. Intriguingly, these studies revealed that Poll II is progressively compartmentalized during the time course of transcriptional activation of HS loci. These transcription """"""""compartments"""""""" are characterized by Poll II being actively recycled rather than a new polymerase being recruited or exchanged by neighboring active HS loci. This compartment could potentially allow recycling of the large battery of factors involved in coactivation, transcription elongation and RNA processing. The features of this compartment and its impact on transcription and gene regulation are targets of this proposal. The overarching hypothesis of this proposal is that live-cell imaging of transcription factors in vivo can provide novel mechanistic insights into the overall architecture of the transcription locus and how this may influence its regulation. Using novel optical imaging technologies, I propose to: (1) Define the properties/dynamics of factors (P-TEFb, Spt6 and CstF-50) that act during different points in transcription cycle and assess if they too are confined components of the transcription """"""""compartment"""""""". (2) Examine how compartment formation influences mRNA trafficking and the rate of mRNA biogenesis at HS loci. (3) Determine the importance of the SCS/SCS'boundary elements and the activity of PARP on the formation and maintenance of the transcription """"""""compartment"""""""". Relevance-Studying gene regulation is of particular relevance to human health, as misregulation of gene activity is a hallmark of many diseases, such as cancer. The primary focus of this project is to better understand the features of transcriptional regulation using the fruit fly model system. Most of the proteins that regulate gene expression in flies have corresponding activities in humans;therefore these studies may provide general insights into gene regulation. Importantly, these studies may also provide insights into how gene regulation may malfunction during human disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32GM087003-02
Application #
7876703
Study Section
Special Emphasis Panel (ZRG1-F05-K (20))
Program Officer
Bender, Michael T
Project Start
2009-06-16
Project End
2012-06-15
Budget Start
2010-06-16
Budget End
2011-06-15
Support Year
2
Fiscal Year
2010
Total Cost
$50,474
Indirect Cost
Name
Cornell University
Department
Biochemistry
Type
Schools of Earth Sciences/Natur
DUNS #
872612445
City
Ithaca
State
NY
Country
United States
Zip Code
14850
Buckley, Martin S; Kwak, Hojoong; Zipfel, Warren R et al. (2014) Kinetics of promoter Pol II on Hsp70 reveal stable pausing and key insights into its regulation. Genes Dev 28:14-9
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
Zobeck, Katie L; Buckley, Martin S; Zipfel, Warren R et al. (2010) Recruitment timing and dynamics of transcription factors at the Hsp70 loci in living cells. Mol Cell 40:965-75