Uncovering a new role of nucleosomes in gene regulation

Information

  • Research Project
  • 9922463
  • ApplicationId
    9922463
  • Core Project Number
    R15GM116102
  • Full Project Number
    3R15GM116102-02S1
  • Serial Number
    116102
  • FOA Number
    PA-18-906
  • Sub Project Id
  • Project Start Date
    9/1/2015 - 8 years ago
  • Project End Date
    3/31/2022 - 2 years ago
  • Program Officer Name
    CARTER, ANTHONY D
  • Budget Start Date
    4/1/2019 - 5 years ago
  • Budget End Date
    3/31/2022 - 2 years ago
  • Fiscal Year
    2019
  • Support Year
    02
  • Suffix
    S1
  • Award Notice Date
    7/29/2019 - 4 years ago

Uncovering a new role of nucleosomes in gene regulation

Project Summary: Uncovering a new role of nucleosomes in gene regulation Transcriptional factors (TFs) and nucleosomes are two major determinants for gene regulation in eukaryotic cells. Traditionally, TFs and nucleosomes are considered to be mutually exclusive. Recent studies have identified a growing list of proteins including the tumor suppressor p53 that are able to bind to nucleosomal DNA without disrupting the overall nucleosome structure. At least for these TFs, nucleosomes are no longer obstacles, and in some cases, nucleosomes can facilitate or even stabilize TF-DNA interactions. However, it was not clear if such interactions (between TFs and nucleosomes) have any biological significance. Our preliminary studies have shown that the extent of accessibility of p53 target sites in nucleosomes correlates with how p53 regulates its target genes, which highlights the importance of nucleosomes in mediating TF binding and controlling gene expression. The proposed research aims to gain full understanding of this new role of nucleosomes in gene regulation. In the Aim 1, we will focus on p53, intending to establish the link between accessibility of p53 binding sites in the context of chromatin and expression patterns of nearby genes. In the Aim 2, we will discover a comprehensive set of potential nucleosomal DNA-binding proteins in humans and model organisms. Nucleosome-TF interactions of interest will be validated by in vitro assays. At the conclusion of these studies, we will have re-defined the roles of nucleosomes in TF binding and gene regulation, developed theoretical and experimental method for testing nucleosome-TF interactions, and established a computational/experimental pipeline to identify nucleosomal DNA-binding proteins.

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R15
  • Administering IC
    GM
  • Application Type
    3
  • Direct Cost Amount
    47300
  • Indirect Cost Amount
    21995
  • Total Cost
    69295
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    859
  • Ed Inst. Type
    SCHOOLS OF ARTS AND SCIENCES
  • Funding ICs
    NIGMS:69295\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
  • Study Section Name
  • Organization Name
    ROCHESTER INSTITUTE OF TECHNOLOGY
  • Organization Department
    OTHER BASIC SCIENCES
  • Organization DUNS
    002223642
  • Organization City
    ROCHESTER
  • Organization State
    NY
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    146235608
  • Organization District
    UNITED STATES