Specification of Anterior-Posterior Identity in the Vertebrae Hindbrain

Information

  • NSF Award
  • 9816905
Owner
  • Award Id
    9816905
  • Award Effective Date
    4/1/1999 - 25 years ago
  • Award Expiration Date
    3/31/2003 - 21 years ago
  • Award Amount
    $ 255,253.00
  • Award Instrument
    Standard Grant

Specification of Anterior-Posterior Identity in the Vertebrae Hindbrain

Moens, C; IBN #9816905 The enormous functional complexity of the vertebrate nervous system is built upon events that occur during early embryogenesis when an initially homogeneous field of cells, the neural plate, is divided and subdivided into progressively more sharply restricted domains. Within the hindbrain, these domains are overtly segmental in character, containing re-iterated sets of neurons and being separated by morphologically and molecularly distinct boundaries. These hindbrain segments, or rhombomeres, acquire their distinct anterior-posterior identities through the action of the hox genes, which also pattern the body segments of invertebrate animals. As such, the vertebrate hindbrain has an archetypal significance as being patterned by mechanisms that are conserved across animal phyla.<br/> This project proposes to study the mechanism by which vertebrates establish anterior-posterior pattern within the hindbrain, and thereby co-opt the hox gens into their segmental body plan. The zebrafish is used as a model system, because its relatively simple nervous system allows the identification of individual neurons at particular anterior-posterior levels within the hindbrain. Thus, it is possible to study the specification and patterning of individual neurons both experimentally, by transplanting them to different anterior-posterior levels, and genetically, by studying mutants in which their organization is disrupted through gene deletions. Using this combination of experimental embryology, molecular biology and genetics, the experiments outlined in this proposal will address when and how individual neurons become committed to their region-specific identities, and what role candidate signalling molecules and candidate signalling sources play in this process.

  • Program Officer
    Marc D. Servetnick
  • Min Amd Letter Date
    3/24/1999 - 25 years ago
  • Max Amd Letter Date
    3/24/1999 - 25 years ago
  • ARRA Amount

Institutions

  • Name
    Fred Hutchinson Cancer Research Center
  • City
    Seattle
  • State
    WA
  • Country
    United States
  • Address
    1100 FAIRVIEW AVE N J6-300
  • Postal Code
    981094433
  • Phone Number
    2066674868

Investigators

  • First Name
    Cecilia
  • Last Name
    Moens
  • Email Address
    cmoens@fhcrc.org
  • Start Date
    3/24/1999 12:00:00 AM

FOA Information

  • Name
    Other Applications NEC
  • Code
    99