Genetic Biochemical Studies of Plant Steroid Signaling

Information

  • Research Project
  • 10254337
  • ApplicationId
    10254337
  • Core Project Number
    R01GM066258
  • Full Project Number
    5R01GM066258-19
  • Serial Number
    066258
  • FOA Number
    PA-19-056
  • Sub Project Id
  • Project Start Date
    8/1/2002 - 22 years ago
  • Project End Date
    6/30/2024 - 8 months ago
  • Program Officer Name
    XU, JIANHUA
  • Budget Start Date
    7/1/2021 - 3 years ago
  • Budget End Date
    6/30/2022 - 2 years ago
  • Fiscal Year
    2021
  • Support Year
    19
  • Suffix
  • Award Notice Date
    8/31/2021 - 3 years ago

Genetic Biochemical Studies of Plant Steroid Signaling

Modified Project Summary/Abstract Section The long-term goal of this project is to understand the molecular networks through which hormones, environmental factors, and nutrients together control plant growth and development. Plants have evolved robust cellular signaling systems to regulate growth and metabolism according to internal status and environmental conditions. Dissecting these plant regulatory systems is important not only for food security and environmental sustainability, but also for understanding cellular regulation in general, as many mechanisms are highly conserved in animals and plants. This research program focuses on the cellular signaling and regulatory network impinged upon by the steroid hormone brassinosteroid (BR), a major growth-promoting hormone that impact a wide range of developmental and physiological processes. Using a combination of genetic, genomic, biochemical, and proteomic approaches in the Arabidopsis model system, we have elucidated molecular mechanisms by which BR binding to receptor kinase BRI1 leads to activation of transcription factor BZR1 through the evolutionarily conserved BSU1 family of phosphatases and GSK3-like kinases. Furthermore, we have revealed at molecular level how the BR signaling pathway is integrated with many other signaling pathways into regulatory networks that control gene transcription program driving cell elongation and various specific developmental programs. Our ongoing research has uncovered many posttranslational mechanisms by which BR signaling directly modulates cellular reorganization and metabolic programs through direct protein-protein interactions and posttranslational modifications. We proposed to focus on these mechanisms that link signaling pathways with major cellular activities such as membrane trafficking, cell division, and carbon metabolism. In addition, we will investigate how BR signaling cross talks with other signaling pathways to balance metabolism with growth demand and to program cellular differentiation in plant development. The research outlined in this proposal will continue to use combinations of genetic and proteomic approaches and will significantly advance our understanding of the molecular mechanisms of cellular signal integration and information processing.

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R01
  • Administering IC
    GM
  • Application Type
    5
  • Direct Cost Amount
    347537
  • Indirect Cost Amount
    213840
  • Total Cost
    561377
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    859
  • Ed Inst. Type
  • Funding ICs
    NIGMS:561377\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    CSRS
  • Study Section Name
    Cellular Signaling and Regulatory Systems Study Section
  • Organization Name
    CARNEGIE INSTITUTION OF WASHINGTON, D.C.
  • Organization Department
  • Organization DUNS
    072641707
  • Organization City
    WASHINGTON
  • Organization State
    DC
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    200051305
  • Organization District
    UNITED STATES