Enhancer Codes with Ligand Mediated Gene Regulation and Chromatin Architecture

Information

  • Research Project
  • 10435941
  • ApplicationId
    10435941
  • Core Project Number
    K01DK121871
  • Full Project Number
    3K01DK121871-03S1
  • Serial Number
    121871
  • FOA Number
    PA-20-272
  • Sub Project Id
  • Project Start Date
    7/1/2019 - 4 years ago
  • Project End Date
    12/31/2022 - a year ago
  • Program Officer Name
    SPAIN, LISA M
  • Budget Start Date
    7/1/2021 - 2 years ago
  • Budget End Date
    12/31/2022 - a year ago
  • Fiscal Year
    2021
  • Support Year
    03
  • Suffix
    S1
  • Award Notice Date
    9/13/2021 - 2 years ago
Organizations

Enhancer Codes with Ligand Mediated Gene Regulation and Chromatin Architecture

Contact PD/PI: Nair, Sreejith Janardhanan PROJECT SUMMARY The central objective of this research proposal is to gain novel insights into the cell biological principles underlying the regulation of gene expression in response to hormonal stimulation. My research focus is gene regulation mediated by transcriptional enhancers. Although recognized as the major organizer of gene regulation in metazoans, the precise mechanism with which enhancer complex assembled and regulate target genes in response to stimuli is still mostly not known. Preliminary data described in this proposal suggest that acutely assembled enhancers harbor ribonucleoprotein complex with a physicochemical property that is quite distinct from that of enhancers that are constitutively active. These enhancers get optimally activated once associated with inter-chromatin granules (ICGs). This proposal will link multiple experimental strategies from disciplines as diverse as molecular biology, biophysics, genomics, proteomics and microscopy to provide a comprehensive understanding of the underlying mechanism of inducible enhancer activation and chromosomal architecture. Together, this approach can significantly alter our current concepts about regulated gene transcriptional programs. Importantly, the finding and experimental skills acquired from this study will also allow the transition to an academic career as an independent investigator studying the biophysical and molecular mechanisms of ligand regulated transcriptional program using proteomic, bioinformatics and genomic approaches. Page 6 Project Summary/Abstract

IC Name
NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES
  • Activity
    K01
  • Administering IC
    DK
  • Application Type
    3
  • Direct Cost Amount
    51830
  • Indirect Cost Amount
    4146
  • Total Cost
    55976
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    847
  • Ed Inst. Type
    ORGANIZED RESEARCH UNITS
  • Funding ICs
    NIDDK:55976\
  • Funding Mechanism
    OTHER RESEARCH-RELATED
  • Study Section
  • Study Section Name
  • Organization Name
    GEORGETOWN UNIVERSITY
  • Organization Department
    NONE
  • Organization DUNS
    049515844
  • Organization City
    WASHINGTON
  • Organization State
    DC
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    200570001
  • Organization District
    UNITED STATES