Identification and Characterization of Causative Genetic Biomarkers for Parkinson

Information

  • Research Project
  • 7801739
  • ApplicationId
    7801739
  • Core Project Number
    R41NS065559
  • Full Project Number
    1R41NS065559-01A1
  • Serial Number
    65559
  • FOA Number
    PA-09-081
  • Sub Project Id
  • Project Start Date
    1/18/2010 - 15 years ago
  • Project End Date
    12/31/2010 - 14 years ago
  • Program Officer Name
    FERTIG, STEPHANIE
  • Budget Start Date
    1/18/2010 - 15 years ago
  • Budget End Date
    12/31/2010 - 14 years ago
  • Fiscal Year
    2010
  • Support Year
    1
  • Suffix
    A1
  • Award Notice Date
    1/18/2010 - 15 years ago

Identification and Characterization of Causative Genetic Biomarkers for Parkinson

DESCRIPTION (provided by applicant): The goal of this project is to rapidly discover biomarkers for Parkinson's Disease (PD) by defining the spectrum of causal genetic loci for PD, not only for the purpose of accurate diagnosis and risk stratification but also in order to shed light on the underlying biology and pathways involved in PD pathogenesis for the purpose of future rational therapeutic development. There are 3 specific aims: 1. To perform array-based high-resolution oligonucleotide comparative genomic hybridization (aCGH) on 100 DNA samples from PD subjects for discovery of causal copy number variants (CNV). This will rely upon a subtractive methodology (PD cohort CNV frequency vs normal control CNV frequency to distinguish disease-specific genomic CNVs) utilizing external (publicly available) CNV databases in combination with an internal pre-existing database generated using a large number of normal individuals. 2. To validate significant PD-specific CNVs through the design of targeted assays (utilizing methods including exon specific MLPA and junction fragment PCR). 3. Having identified and validated PD-specific CNVs, to study in greater depth those that are the most promising (on the basis of frequency and genes implicated), by rapidly interrogating the total PD cohort (utilizing exon specific MLPA as well as next-generation sequencing, in order to cover any possible mutational mechanism), by comparison with a large number of normal control samples. PUBLIC HEALTH RELEVANCE: There is no doubt that the only rational approach to future therapeutic interventions in common disorders, such as Parkinson's Disease (PD), is one that will be based on a more precise knowledge of the underlying biological causes of such disorders. The successful application of genome wide copy number analysis for biomarker development in PD will facilitate improved diagnostic testing and risk stratification as well as yielding insight into the underlying pathogenesis of PD, paving the way for research into specific interventions, whether pharmaceutical or otherwise.

IC Name
NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE
  • Activity
    R41
  • Administering IC
    NS
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    199281
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    853
  • Ed Inst. Type
  • Funding ICs
    NINDS:199281\
  • Funding Mechanism
    SBIR-STTR
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    POPULATION DIAGNOSTICS, INC.
  • Organization Department
  • Organization DUNS
    806706144
  • Organization City
    MELVILLE
  • Organization State
    NY
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    117473821
  • Organization District
    UNITED STATES