This proposal concerns the cellular, genetic and molecular basis for the formation of the prechordal plate which can act as an inductive center. The foundation for the studies originates from a mutagenesis screen of the zebrafish genome and discovering 6 loci which affect prechordal plate development or function. One of these mutants, one-eyed pinhead (oep), is required in prospective prechordal plate cells by the onset of gastrulation as defined by various molecular markers. The notochord is unaffected in the oep mutant so the gene could be involved in the segregation of the prechordal plate lineage and acts autonomously as judged from labeling studies. There are three alleles available at the locus, two ENU induced and one by irradiation.
The first aim will be to determine the origin and behavior of prechordal plate cells in pregastrula wildtype and oep embryos. The question being posed is when do the prechordal plate cells become distinct from other dorsal cell types and become regionalized? Classical fate mapping will be performed by labeling single cells before gastrulation and following their lineage by time-lapse video microscopy. Additionally, labeled wildtype and oep mutant cells will be co-transplanted into unlabeled hosts and their behavior and fate will be compared.
The second aim will attempt to isolate and identify the oep gene using the current methodologies available such as exon trap. The third specific aim involves the characterization of the other loci which affect prechordal development. Additional alleles will be generated at the loci with further phenotypic characterization and epistatic relationships to oep being established. Also the mutations will be placed on the zebrafish genetic map.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM056211-04
Application #
6180850
Study Section
Human Embryology and Development Subcommittee 1 (HED)
Program Officer
Zatz, Marion M
Project Start
1997-09-01
Project End
2002-08-31
Budget Start
2000-09-01
Budget End
2001-08-31
Support Year
4
Fiscal Year
2000
Total Cost
$260,747
Indirect Cost
Name
New York University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
City
New York
State
NY
Country
United States
Zip Code
10016
Almuedo-Castillo, María; Bläßle, Alexander; Mörsdorf, David et al. (2018) Scale-invariant patterning by size-dependent inhibition of Nodal signalling. Nat Cell Biol 20:1032-1042
Freyer, Laina; Hsu, Chih-Wei; Nowotschin, Sonja et al. (2017) Loss of Apela Peptide in Mice Causes Low Penetrance Embryonic Lethality and Defects in Early Mesodermal Derivatives. Cell Rep 20:2116-2130
Rogers, Katherine W; Lord, Nathan D; Gagnon, James A et al. (2017) Nodal patterning without Lefty inhibitory feedback is functional but fragile. Elife 6:
Montague, Tessa G; Schier, Alexander F (2017) Vg1-Nodal heterodimers are the endogenous inducers of mesendoderm. Elife 6:
Norris, Megan L; Pauli, Andrea; Gagnon, James A et al. (2017) Toddler signaling regulates mesodermal cell migration downstream of Nodal signaling. Elife 6:
Thyme, Summer B; Akhmetova, Laila; Montague, Tessa G et al. (2016) Internal guide RNA interactions interfere with Cas9-mediated cleavage. Nat Commun 7:11750
McKenna, Aaron; Findlay, Gregory M; Gagnon, James A et al. (2016) Whole-organism lineage tracing by combinatorial and cumulative genome editing. Science 353:aaf7907
Thyme, Summer B; Schier, Alexander F (2016) Polq-Mediated End Joining Is Essential for Surviving DNA Double-Strand Breaks during Early Zebrafish Development. Cell Rep 15:707-714
Chew, Guo-Liang; Pauli, Andrea; Schier, Alexander F (2016) Conservation of uORF repressiveness and sequence features in mouse, human and zebrafish. Nat Commun 7:11663
Li-Villarreal, Nanbing; Forbes, Meredyth M; Loza, Andrew J et al. (2016) Dachsous1b cadherin regulates actin and microtubule cytoskeleton during early zebrafish embryogenesis. Development 143:1832

Showing the most recent 10 out of 54 publications