The broad objective of this research is to determine how the morphogenetic movements of amphibian neurulation are controlled by tissue interactions. The specific objective is to test the hypothesis that the detailed shaping of the neural anlagen of the amphibian, Xenopus laevis is controlled by two tissue interactions: 1) an edgewise induction of the dorsal ectoderm by the dorsal axial mesoderm to produce simple lengthening (extension) and narrowing (convergence) of the neural plate; 2) a basal induction of the dorsal ecotderm by dorsal mesoderm to produce cell shape changes (columnarization and wedging) in the dorsal ectoderm. Furthermore, we predict that the type of dorsal mesoderm will determine what cell shape changes are induced. We have been able to obtain different morphogenetic reswponses from dorsal ecectoderm, depending on the type of mesoderm used as an inductor and whether it is placed edgewise to the ectoderm or beneath it. We will test the above two-inductor hypothesis by explanting dorsal, axial mesoderm, or parts of it, and placing it in edgewise or basal apposition to specific regions of the ectoderm. We will monitor the degrtee and pattern of extension and convergence with high resolution video-optical disk recordings and cell shape changes in cross-fractured material with SEM. By using these two inductive routes to call forth different morphogenetic components of neural plate morphogenesis, separately and together, we hope to characterize the role of each in the overall process. These results will be basic to our understanding of the early steps in neural development of vertebrates and the methods and concepts developed will be applicable to a variety of other apporaches to analysis of neurogenesis at the molecular and cellular levels.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
1R01HD025594-01
Application #
3326773
Study Section
Neurology B Subcommittee 1 (NEUB)
Project Start
1989-04-01
Project End
1992-03-31
Budget Start
1989-04-01
Budget End
1990-03-31
Support Year
1
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of California Berkeley
Department
Type
Schools of Arts and Sciences
DUNS #
094878337
City
Berkeley
State
CA
Country
United States
Zip Code
94704
Pfister, Katherine; Shook, David R; Chang, Chenbei et al. (2016) Molecular model for force production and transmission during vertebrate gastrulation. Development 143:715-27
Edlund, Anna F; Davidson, Lance A; Keller, Raymond E (2013) Cell segregation, mixing, and tissue pattern in the spinal cord of the Xenopus laevis neurula. Dev Dyn 242:1134-46
Skoglund, Paul; Keller, Ray (2010) Integration of planar cell polarity and ECM signaling in elongation of the vertebrate body plan. Curr Opin Cell Biol 22:589-96
Rolo, Ana; Skoglund, Paul; Keller, Ray (2009) Morphogenetic movements driving neural tube closure in Xenopus require myosin IIB. Dev Biol 327:327-38
Shook, David R; Keller, Ray (2008) Morphogenic machines evolve more rapidly than the signals that pattern them: lessons from amphibians. J Exp Zool B Mol Dev Evol 310:111-35
Keller, Ray; Poznanski, Ann; Elul, Tamira (2008) Experimental embryological methods for analysis of neural induction in the amphibian. Methods Mol Biol 461:405-46
Davidson, Lance A; Dzamba, Bette D; Keller, Ray et al. (2008) Live imaging of cell protrusive activity, and extracellular matrix assembly and remodeling during morphogenesis in the frog, Xenopus laevis. Dev Dyn 237:2684-92
Shook, David R; Keller, Ray (2008) Epithelial type, ingression, blastopore architecture and the evolution of chordate mesoderm morphogenesis. J Exp Zool B Mol Dev Evol 310:85-110
Goto, Toshiyasu; Keller, Ray; Asashima, Makoto (2008) Concentrations of TATA box-binding protein (TBP)-type genes affect chordamesodermal gene expression. Int J Dev Biol 52:371-5
Davidson, Lance A; Marsden, Mungo; Keller, Raymond et al. (2006) Integrin alpha5beta1 and fibronectin regulate polarized cell protrusions required for Xenopus convergence and extension. Curr Biol 16:833-44

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