Mapping Neural Connectivity in Zebrafish Larvae Using a Photoconvertible Protein

Information

  • Research Project
  • 9855836
  • ApplicationId
    9855836
  • Core Project Number
    SC2GM130485
  • Full Project Number
    1SC2GM130485-01A1
  • Serial Number
    130485
  • FOA Number
    PAR-16-438
  • Sub Project Id
  • Project Start Date
    7/1/2020 - 4 years ago
  • Project End Date
    6/30/2023 - a year ago
  • Program Officer Name
    BERNAL, FEDERICO
  • Budget Start Date
    7/1/2020 - 4 years ago
  • Budget End Date
    6/30/2021 - 3 years ago
  • Fiscal Year
    2020
  • Support Year
    01
  • Suffix
    A1
  • Award Notice Date
    6/30/2020 - 4 years ago

Mapping Neural Connectivity in Zebrafish Larvae Using a Photoconvertible Protein

PROJECT SUMMARY Creation of whole-brain functional connectomes will facilitate a holistic understanding of memory formation, which is a major goal of modern neuroscience. Information gained from understanding the functional connections between neurons and the underlying plasticity between connections can be used to understand and treat neurological and mental disorders. In vivo whole-brain mapping with current technologies requires advantageous biological attributes in combination with a substantial molecular toolbox. Two invertebrate model organisms have these properties: D. melanogaster and C. elegans. However, zebrafish (Danio rerio) is the only vertebrate species with this capacity. The ability to form a functional connectome with larval zebrafish affords distinct advantages to understanding memory formation or pinpointing aberrant neural circuits in animal models of human disorders. Further, rapid development, small size, and high fecundity of zebrafish makes them an ideal organism for high- throughput screening, a useful mechanism to discover novel therapeutics for these disorders. The project will attempt to create a new tool to rapidly form in vivo whole-brain connectomes in freely moving fish with the long-term goal of understanding brain function and dysfunction at a circuit-level. Towards this goal, we will create transgenic fish that express a photoconvertible protein under the control of activity- dependent promoters. We will then determine the experimental procedures for each line of transgenic fish that most efficiently and accurately reflect the neural activity under investigation and minimize signals related to nonspecific neural activity. After we have defined the experimental potential and constraints of our transgenic lines of fish, we will seek to determine if the recorded neural activity is physiologically valid. To do so, we will form functional maps of neural activity in response to stimulation of sensory systems with previously defined neural connections. These experiments should provide the pilot data necessary to begin investigating changes in functional connectomes due to memory formation in zebrafish models of neurodevelopmental disorders. Data from the proposed studies are expected to facilitate the development of effective treatments for brain diseases and disorders, including Alzheimer's disease, PTSD, schizophrenia and autism.

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    SC2
  • Administering IC
    GM
  • Application Type
    1
  • Direct Cost Amount
    100000
  • Indirect Cost Amount
    10985
  • Total Cost
    110985
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    859
  • Ed Inst. Type
    SCHOOLS OF ARTS AND SCIENCES
  • Funding ICs
    NIGMS:110985\
  • Funding Mechanism
    OTHER RESEARCH-RELATED
  • Study Section
    ZGM1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    CALIFORNIA STATE UNIVERSITY FULLERTON
  • Organization Department
    PSYCHOLOGY
  • Organization DUNS
    106670755
  • Organization City
    FULLERTON
  • Organization State
    CA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    928313014
  • Organization District
    UNITED STATES