Genetic Regulation of Skeletal Muscle Repair

Information

  • Research Project
  • 7633335
  • ApplicationId
    7633335
  • Core Project Number
    R01AR044031
  • Full Project Number
    5R01AR044031-13
  • Serial Number
    44031
  • FOA Number
  • Sub Project Id
  • Project Start Date
    7/15/1996 - 27 years ago
  • Project End Date
    4/30/2010 - 14 years ago
  • Program Officer Name
    BOYCE, AMANDA T.
  • Budget Start Date
    5/1/2009 - 15 years ago
  • Budget End Date
    4/30/2010 - 14 years ago
  • Fiscal Year
    2009
  • Support Year
    13
  • Suffix
  • Award Notice Date
    5/28/2009 - 15 years ago

Genetic Regulation of Skeletal Muscle Repair

DESCRIPTION (provided by applicant): Regenerative myogenesis is the formation of muscle progenitors during the repair of adult skeletal muscle following tissue trauma. In this application, we outline a research program to molecularly define the genetic mechanisms through which Pax7 enforces lineage commitment during regenerative myogenesis. To fully define the Pax7 regulome in primary myoblasts, Pax7 bound to fragmented chromatin will be immunoprecipitated and the DNA isolated and subjected to a subtractive PCR-based procedure to selectively amplify Pax7 binding sites. Direct targets will be identified by a comparative analysis between our existing microarray data, and regulatory regions that recruit Pax7. The function of a select set of prioritized candidate target genes will be investigated using molecular and genetic approaches. Real-time PCR will be used to characterize cell-type and differentiation patterns of expression. Knock down experiments will be performed with RNAi, and full-length cDNAs over-expressed in myoblasts. Lastly, the binding of Pax7 alternative splice forms to candidate promoters will be evaluated. To investigate the hypothesis that Pax7 recruits co-factors to facilitate appropriate regulation of target genes, the ability of Pax7 to direct acetyl-transferase activity will be investigated, and chromatin immunoprecipitation assays will be used to characterize the histone modifications over Pax7 target promoters. A genome wide assessment of histone modifications using microarrays will be conducted. To elucidate Pax7 function, we will isolate and identify protein components of the Pax7 transcriptional complex by mass spectroscopy. These experimental approaches will facilitate a molecular understanding of Pax7 function and the genomic definition of the chromatin domains established by Pax7. Understanding the molecular mechanism regulating gene function during muscle regeneration will provide insights that will potentially lead to new modalities of therapeutic intervention for the treatment of muscle degenerative disease.

IC Name
NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES
  • Activity
    R01
  • Administering IC
    AR
  • Application Type
    5
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    204429
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    846
  • Ed Inst. Type
  • Funding ICs
    NIAMS:204429\
  • Funding Mechanism
    Research Projects
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    OTTAWA HOSPITAL RESEARCH INSTITUTE
  • Organization Department
  • Organization DUNS
    201768095
  • Organization City
    OTTAWA
  • Organization State
    ON
  • Organization Country
    CANADA
  • Organization Zip Code
    K1Y 4E9
  • Organization District
    CANADA