Genetic neuroscience: How human genes and alleles shape neuronal phenotypes

Information

  • Research Project
  • 10223999
  • ApplicationId
    10223999
  • Core Project Number
    U01MH115727
  • Full Project Number
    5U01MH115727-05
  • Serial Number
    115727
  • FOA Number
    PAR-17-179
  • Sub Project Id
  • Project Start Date
    9/20/2017 - 7 years ago
  • Project End Date
    7/31/2022 - 2 years ago
  • Program Officer Name
    ARGUELLO, ALEXANDER
  • Budget Start Date
    8/1/2021 - 3 years ago
  • Budget End Date
    7/31/2022 - 2 years ago
  • Fiscal Year
    2021
  • Support Year
    05
  • Suffix
  • Award Notice Date
    9/3/2021 - 3 years ago
Organizations

Genetic neuroscience: How human genes and alleles shape neuronal phenotypes

Genetic studies have identified many specific loci with significant associations to psychiatric disorders. However, unless we can develop useful approaches for systematically turning genetic information into neurobiological insights about brain disorders, there is a danger that costly and hard-won genetic findings will not be exploitable to understand pathophysiology and generate important therapeutic hypotheses. The goal of our collaborative, interdisciplinary effort is to develop powerful, generalizable approaches for discovering how risk variants for psychiatric disorders shape neurobiological processes at multiple levels of analysis, and to identify the processes whose dysregulation underlies disease. To do this, we propose to develop new experimental and inferential systems to bridge a longstanding gap between human genetics and experimental biology. We aim to identify biological causes and effects that span the genetic, molecular, and cellular levels of the nervous system. Our interdisciplinary team will develop new experimental systems that measure genetic influences across levels of analysis (RNA, proteins, and cellular function including physiology) in precise, scalable, well- controlled ways. We will make use of emerging cellular systems including three-dimensional cortical spheroids and organoids, and radically novel ?population in a dish? experimental systems that collect data on cells from hundreds of donors in a shared environment, inferring donor identity at the time of phenotypic readout. The analysis of such systems in turn requires sophisticated inferential strategies and new ideas from computer science. We propose to develop and widely share experimental and computational resources, including cell lines, methods, datasets, and analytic tools. The successful completion of this work will identify key neurobiological processes for multiple psychiatric disorders, and fortify many other scientists in making such connections in their own work. We hope in so doing to create a new kind of interdisciplinary science that ? by combining the strengths of data-driven, unbiased human genetics with the power of emerging experimental systems ? transforms the rate at which human- genetic leads lead to insights about disease mechanisms.

IC Name
NATIONAL INSTITUTE OF MENTAL HEALTH
  • Activity
    U01
  • Administering IC
    MH
  • Application Type
    5
  • Direct Cost Amount
    2860176
  • Indirect Cost Amount
    1166410
  • Total Cost
    4026586
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    242
  • Ed Inst. Type
  • Funding ICs
    NIMH:4026586\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    BROAD INSTITUTE, INC.
  • Organization Department
  • Organization DUNS
    623544785
  • Organization City
    CAMBRIDGE
  • Organization State
    MA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    021421027
  • Organization District
    UNITED STATES