Using Time-Resolved Genetics to Determine the Function of PI3-Kinase Signaling in

Information

  • Research Project
  • 7455498
  • ApplicationId
    7455498
  • Core Project Number
    R15MH083221
  • Full Project Number
    1R15MH083221-01
  • Serial Number
    83221
  • FOA Number
    PA-06-42
  • Sub Project Id
  • Project Start Date
    4/1/2008 - 16 years ago
  • Project End Date
    3/31/2011 - 13 years ago
  • Program Officer Name
    MAMOUNAS, LAURA
  • Budget Start Date
    4/1/2008 - 16 years ago
  • Budget End Date
    3/31/2011 - 13 years ago
  • Fiscal Year
    2008
  • Support Year
    1
  • Suffix
  • Award Notice Date
    3/13/2008 - 16 years ago
Organizations

Using Time-Resolved Genetics to Determine the Function of PI3-Kinase Signaling in

[unreadable] DESCRIPTION (provided by applicant): The main function of the brain, or nervous system, is to receive inputs from the environment, process that information, and then tell the rest of the body what to do. The brain does this with an extremely complex array of nerve cells (neurons), whose main function is to connect with and talk to other neurons. In order to form these networks of functional connections, neurons must acquire an elaborate structure, including complex branching patterns of axons and dendrites. Thus, identification of the genes that control the acquisition of these elaborate cell shapes is important for understanding how the nervous system develops, and may also provide insights into what goes wrong in disease states of mental health. To identify the genes involved in the morphological differentiation of neurons, we will develop a time-resolved genetic loss-of-function approach that can be used in the zebrafish model organism. By in vivo electroporation of morpholino antisense oligonucleotides, we can knockdown expression of a particular gene at a specific time in development. Through the same method, we can incorporate expression plasmids that code for the green fluorescent protein (GFP), which allows us to use fluorescence microscopy to visualize the changes in cell shape that occur during development in live zebrafish embryos. Thus, we can examine whether a target gene of interest is important for morphological differentiation by examining whether loss-of-function of that gene leads to defects in the changes in cell shape visualized with GFP. The target genes that we are interested in are those that translate the signals received from the complex extracellular environment into a cell biological response resulting in changes in cells shape. The phosphoinositide 3-kinase signaling pathway has been implicated in similar processes. We will examine whether PI3-kinase signaling is required for morphological differentiation of neurons by knocking down expression of the p110 catalytic subunit of the kinase, and then examining whether or not neurons still acquire their distinct shapes. [unreadable] PUBLIC HEALTH RELEVANCE: Identifying the genes that control the development of the vertebrate brain is important for understanding what might be defective in disease states, and for identifying drug targets for therapy. Also, knowing which genes are important for guiding the growth of neurons during development may also provide drug target to be re-activated to facilitate regeneration of the nervous system after damage or disease. This project aims to identify the genes involved in development of the nervous system by selectively deleting specific genes and then visualizing changes in the structure of neurons in the zebrafish model organism. [unreadable] [unreadable] [unreadable]

IC Name
NATIONAL INSTITUTE OF MENTAL HEALTH
  • Activity
    R15
  • Administering IC
    MH
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    205819
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    242
  • Ed Inst. Type
    SCHOOLS OF ARTS AND SCIENCES
  • Funding ICs
    NIMH:205819\
  • Funding Mechanism
  • Study Section
    NCF
  • Study Section Name
    Neurogenesis and Cell Fate Study Section
  • Organization Name
    PACE UNIVERSITY NEW YORK
  • Organization Department
    BIOLOGY
  • Organization DUNS
    064961022
  • Organization City
    NEW YORK
  • Organization State
    NY
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    10038
  • Organization District
    UNITED STATES