Sunday, November 24, 2024
11/24/2024
DESCRIPTION (provided by applicant): The Principal Investigator's (PI's) laboratory studies transcriptional regulation of the human LAT gene, which encodes a transmembrane adaptor protein linking receptor engagement to the activation of numerous downstream signaling pathways. This gene, highly conserved among mammals, is critical for the development and/or function of T cells, mast cells, Natural Killer cells, and megakaryocytes/platelets. The specific aims outlined in this grant proposal build upon previous findings from the PI's lab and also initiate new studies focused on the contribution of distal control regions in the transcriptional regulation of LAT. The specific aims of this grant proposal are to: 1. Use gene knockdown experiments to explore the functional contribution of Ets1, Elf1, and Runx1 in LAT gene expression. A demonstrated role for these transcription factors will be followed by investigations that examine the underlying mechanism by which they operate and will focus on their modulation of histone acetylation levels within the promoter region. 2. Employ systematic promoter deletions, chromatin immunoprecipitation assays, gene knockdown experiments, and other laboratory techniques to delineate and characterize additional critical control regions within the proximal LAT promoter that have yet to be examined in detail. 3. Implement reporter gene assays to investigate putative distal control regions that display a number of features consistent with their role as enhancer elements for the LAT gene. Confirmation that one or more of these regions serve as an enhancer will be followed by experiments to map the important regulatory sites and characterize interacting proteins. This specific aim will also include chromatin conformation capture experiments to determine if the enhancer element(s) interact with the LAT proximal promoter region. This project will provide important new insights into the specific molecular processes that control transcription of the human LAT gene. As the details of LAT gene regulation continue to emerge, it may be possible to use this knowledge to devise intervention strategies that alter LAT expression as a means of modulating the immune responses and/or platelet function in situations where it would be therapeutically beneficial. This research will also aid in further understanding the general principles that govern gene regulation in eukaryotes. Finally, this research will provide an opportunity to integrate research and learning at Agnes Scott College, a small liberal arts college for women. Undergraduate students will contribute to each of the specific aims outlined in this proposal. Aspects of this research will also be incorporated into courses that the PI teaches.
HHS’ Tracking Accountability in Government Grants System (TAGGS) website provides access to detailed descriptions of grants, loans, aggregated direct payments and other types of financial assistance awarded by the HHS Operating Divisions (OPDIVs) and the Office of the Secretary Staff Divisions (STAFFDIVs).
