We have discovered a secreted, soluble protein that is able to inhibit primary neurogenesis in Xenopus embryos. This 394 amino acid protein contains three serine proteinase inhibitor domains of the Kunitz class. This novel protein has been named Trinein and was isolated during a differential screen for maternally-encoded mRNAs present in the Xenopus laevis egg. Strikingly, microinjection of Trinein mRNA into Xenopus embryos seems to have little effect on mesodermal (marked by Xbra, sonic hedgehog, chordin) and neural plate (marked by Sox-2) cell differentiation; however, differentiation of definitive mature neurons (positive for neurotubulin and neurogenin) is blocked in the neural plate (unpublished data). This proposal builds upon these functional data of Trinein to understand its function in mammalian neurogenesis.

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 #
5F32HD040708-03
Application #
6655695
Study Section
Special Emphasis Panel (ZRG1-MDCN-6 (01))
Program Officer
Henken, Deborah B
Project Start
2002-05-15
Project End
Budget Start
2003-05-15
Budget End
2004-05-14
Support Year
3
Fiscal Year
2003
Total Cost
$48,148
Indirect Cost
Name
University of California Los Angeles
Department
Biochemistry
Type
Schools of Medicine
DUNS #
092530369
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Wessely, Oliver; Kim, James I; Tran, Uyen et al. (2005) xBtg-x regulates Wnt/beta-Catenin signaling during early Xenopus development. Dev Biol 283:17-28
Wessely, Oliver; Kim, James I; Geissert, Douglas et al. (2004) Analysis of Spemann organizer formation in Xenopus embryos by cDNA macroarrays. Dev Biol 269:552-66