We have found that inhibition of the MAPK p38 in sea urchin embryos results in the disruption of larval skeletal patterning. Patterning involves the interaction of ectoderm and mesoderm, but the mechanism and molecular details are unknown in this and other patterning models, such as the vertebrate limb or the insect imaginal disc.
In Aim 1, we will assess whether patterning cues within the ectoderm are local or global by expressing p38 mutants in restricted ectodermal regions.
In Aim 2, we will characterize the interaction of ectoderm and mesoderm, and assess the contribution of thin filopodia to the transduction of patterning signals.
In Aim 3, we will identify proteins involved in patterning through the use of subtractive hybridization. Together, the results of this study will define the molecules and mechanisms underlying embryonic pattern formation in a simple model system.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32HD041802-01
Application #
6445448
Study Section
Cell Development and Function Integrated Review Group (CDF)
Program Officer
Klein, Steven
Project Start
2002-03-01
Project End
Budget Start
2002-03-01
Budget End
2003-02-28
Support Year
1
Fiscal Year
2002
Total Cost
$46,192
Indirect Cost
Name
Duke University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
071723621
City
Durham
State
NC
Country
United States
Zip Code
27705
Bradham, Cynthia A; Oikonomou, Catherine; Kühn, Alexander et al. (2009) Chordin is required for neural but not axial development in sea urchin embryos. Dev Biol 328:221-33
Bradham, Cynthia A; McClay, David R (2006) p38 MAPK is essential for secondary axis specification and patterning in sea urchin embryos. Development 133:21-32
Bradham, C A; Miranda, E L; McClay, D R (2004) PI3K inhibitors block skeletogenesis but not patterning in sea urchin embryos. Dev Dyn 229:713-21