Molecular Mechanism of Akirin Function During Myogenesis

Information

  • Research Project
  • 8497302
  • ApplicationId
    8497302
  • Core Project Number
    R15GM102826
  • Full Project Number
    1R15GM102826-01A1
  • Serial Number
    102826
  • FOA Number
    PA-12-006
  • Sub Project Id
  • Project Start Date
    5/1/2013 - 11 years ago
  • Project End Date
    4/30/2017 - 7 years ago
  • Program Officer Name
    HOODBHOY, TANYA
  • Budget Start Date
    5/1/2013 - 11 years ago
  • Budget End Date
    4/30/2017 - 7 years ago
  • Fiscal Year
    2013
  • Support Year
    01
  • Suffix
    A1
  • Award Notice Date
    4/12/2013 - 11 years ago

Molecular Mechanism of Akirin Function During Myogenesis

DESCRIPTION (provided by applicant): The specification and differentiation of myoblasts by the action of myogenic transcription factors is a key event in the formation of the skeletal musculature. Following embryonic muscle development, the specification and differentiation of myoblasts remains essential for the maintenance and regeneration of healthy adult muscle in mammals. Failure to maintain muscle homeostasis properly through the establishment of new populations of myoblasts leads to progressive degenerative muscle wasting. However, despite the primary importance of myoblast specification and differentiation for myogenesis, the identities of new molecular players in this process remain unknown. Preliminary studies in the fruit fly, Drosophila melanogaster, have recently identified a novel participant in myogenesis, the conserved nuclear protein Akirin. Akirin appears to play an important yet still unidentified role i the regulation of gene expression during myoblast specification. The overall goal of this proposal is to use Drosophila to identify and characterize the molecular mechanism of gene regulation by Akirin during myogenesis. The rationale for the proposed research is that through understanding the modes of action of novel regulators of myogenesis such as Akirin, the efficacy of therapies aimed at mitigating or reversing muscle wasting can be improved. We will study Akirin's mode of action through two specific aims. First, we will perform deletion analysis to identify the domains of interaction between Akirin and the transcriptional machinery that are critical for Akirin-mediated gene regulation. Second, we will use a double heterozygote assay to identify candidate proteins that interact with Akirin during muscle development, and are essential cofactors for Akirin-mediated gene regulation. Critically, in keeping with the goals of the AREA award mechanism, this project will give undergraduate researchers hands-on experience in a wide variety of molecular, genetic and biochemical techniques, which will provide a valuable skill set for a future career in biomedical research.

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R15
  • Administering IC
    GM
  • Application Type
    1
  • Direct Cost Amount
    228000
  • Indirect Cost Amount
    81977
  • Total Cost
    309977
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    859
  • Ed Inst. Type
    SCHOOLS OF ARTS AND SCIENCES
  • Funding ICs
    NIGMS:309977\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    DEV2
  • Study Section Name
    Development - 2 Study Section
  • Organization Name
    KENNESAW STATE UNIVERSITY
  • Organization Department
    PHYSICS
  • Organization DUNS
    627758923
  • Organization City
    KENNESAW
  • Organization State
    GA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    301445588
  • Organization District
    UNITED STATES