The role of CTCF in establishing and maintaining chromatin architecture during M. musculus spermatogenesis

Information

  • Research Project
  • 9880872
  • ApplicationId
    9880872
  • Core Project Number
    R15GM135793
  • Full Project Number
    1R15GM135793-01
  • Serial Number
    135793
  • FOA Number
    PAR-18-714
  • Sub Project Id
  • Project Start Date
    9/19/2019 - 5 years ago
  • Project End Date
    8/31/2022 - 2 years ago
  • Program Officer Name
    CARTER, ANTHONY D
  • Budget Start Date
    9/19/2019 - 5 years ago
  • Budget End Date
    8/31/2022 - 2 years ago
  • Fiscal Year
    2019
  • Support Year
    01
  • Suffix
  • Award Notice Date
    9/19/2019 - 5 years ago
Organizations

The role of CTCF in establishing and maintaining chromatin architecture during M. musculus spermatogenesis

Title: AREA R15 application - The role of CTCF in establishing and maintaining chromatin architecture during M. musculus spermatogenesis With the completion of the Human Genome Project in 2003 and the 1000 Genomes Project in 2012, scientists have gained deep understanding of the genetic variation within the human genome, yet with the recent discovery of the inheritance of acquired states (transgenerational inheritance), our understanding of the way in which traits can be passed from parent to offspring has dramatically changed. Though the study of transgenerational inheritance has recently pushed many exciting new boundaries, fundamental questions remain about the more basic functional roles of underlying epigenetic mechanisms. In order for epigenetic patterns to pass from parent to offspring, epigenetic marks must be established during gametogenesis and transmitted to offspring. One of the most widely studied epigenetic marks is chromatin organization yet despite a recent interest in the specialized chromatin patterning exhibited in mammalian gametes, the functional consequence of these patterns remains unknown. Using a specialized suite of molecular tools unique to our laboratory, the study proposed here will focus on the link between the essential DNA binding factor CTCF and the unique chromatin architecture established during spermatogenesis in M. musculus. In line with the goals of the NIH AREA research grant program, students performing the research funded by this proposal at Rowan University will be directly involved in cutting edge molecular biology research techniques while at the same time working on a hypothesis-driven project which has the potential to significantly affect the way in which we approach epigenetic inheritance. The completion of this research project at Rowan will continue to push forward our mission of addressing paradigm-shifting scientific problems while providing students with the best possible avenue to engage in the latest scientific practices to develop highly-trained contributors to the scientific community.

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R15
  • Administering IC
    GM
  • Application Type
    1
  • Direct Cost Amount
    297091
  • Indirect Cost Amount
    148546
  • Total Cost
    445637
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    859
  • Ed Inst. Type
    SCHOOLS OF ARTS AND SCIENCES
  • Funding ICs
    NIGMS:445637\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    MGB
  • Study Section Name
    Molecular Genetics B Study Section
  • Organization Name
    ROWAN UNIVERSITY
  • Organization Department
    BIOLOGY
  • Organization DUNS
    139203145
  • Organization City
    GLASSBORO
  • Organization State
    NJ
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    080281700
  • Organization District
    UNITED STATES