The establishment of functional neural circuits in the vertebrate central nervous system depends on the correct partial positioning of distinct neural cell types. In the hindbrain this is facilitated by the appearance of segments, or rhombomeres, that act as lineage-restricted compartments in which developmental programs are reiterated. Hindbrain neural crest contributes to the structural and neuronal components of the head and neck, and disruption of the early patterning of the hindbrain results both in neurological and craniofacial defects in humans. The long-term goal of this research is to understand how hindbrain segmentation is established, how segments acquire distinct identities and how these identities result in the specification of functionally distinct neuronal cell types. The zebrafish, suited to both genetic analysis and experimental embryology, is used as a model system in which to address these questions. Lazarus and valentino are zebrafish hindbrain segmentation genes that were identified in a screen for zebrafish mutants in which hindbrain patterning is disrupted. The proposed experiments use these mutants to address the genetic and molecular basis of head segmentation as follows: (1) Genetic analysis of lazarus will address whether its function is required within the hindbrain or in the periphery to bring about global segmentation in the head. Positional cloning will establish its molecular mechanism and its position in the hierarchy of hindbrain segmentation. (2) The role of valentino in hindbrain segmentation will be studied by identifying molecular partners with which it interacts in order to subdivide rhombomeres 5 and 6 from their common precursor in the presumptive hindbrain. (3) The hypothesized role of Eph receptors and their ligands in mediating repulsive cell-cell interactions in the hindbrain will be examined by assaying the effects of Eph and ephrin expression on the characteristic behaviors of valentino and lazarus mutant cells in genetic mosaics.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD037909-03
Application #
6388139
Study Section
Special Emphasis Panel (ZRG1-MDCN-6 (01))
Program Officer
Henken, Deborah B
Project Start
1999-08-01
Project End
2004-05-31
Budget Start
2001-06-01
Budget End
2002-05-31
Support Year
3
Fiscal Year
2001
Total Cost
$210,093
Indirect Cost
Name
Fred Hutchinson Cancer Research Center
Department
Type
DUNS #
075524595
City
Seattle
State
WA
Country
United States
Zip Code
98109
Su, Chen-Ying; Kemp, Hilary A; Moens, Cecilia B (2014) Cerebellar development in the absence of Gbx function in zebrafish. Dev Biol 386:181-90
Zigman, Mihaela; Laumann-Lipp, Nico; Titus, Tom et al. (2014) Hoxb1b controls oriented cell division, cell shape and microtubule dynamics in neural tube morphogenesis. Development 141:639-49
Miller, Adam C; Obholzer, Nikolaus D; Shah, Arish N et al. (2013) RNA-seq-based mapping and candidate identification of mutations from forward genetic screens. Genome Res 23:679-86
Mapp, Oni M; Walsh, Gregory S; Moens, Cecilia B et al. (2011) Zebrafish Prickle1b mediates facial branchiomotor neuron migration via a farnesylation-dependent nuclear activity. Development 138:2121-32
Žigman, Mihaela; Trinh, Le A; Fraser, Scott E et al. (2011) Zebrafish neural tube morphogenesis requires Scribble-dependent oriented cell divisions. Curr Biol 21:79-86
Bachmann-Gagescu, Ruxandra; Phelps, Ian G; Stearns, George et al. (2011) The ciliopathy gene cc2d2a controls zebrafish photoreceptor outer segment development through a role in Rab8-dependent vesicle trafficking. Hum Mol Genet 20:4041-55
Walsh, Gregory S; Grant, Paul K; Morgan, John A et al. (2011) Planar polarity pathway and Nance-Horan syndrome-like 1b have essential cell-autonomous functions in neuronal migration. Development 138:3033-42
Feng, L; Hernandez, R E; Waxman, J S et al. (2010) Dhrs3a regulates retinoic acid biosynthesis through a feedback inhibition mechanism. Dev Biol 338:1-14
Grant, Paul K; Moens, Cecilia B (2010) The neuroepithelial basement membrane serves as a boundary and a substrate for neuron migration in the zebrafish hindbrain. Neural Dev 5:9
Kemp, Hilary A; Cooke, Julie E; Moens, Cecilia B (2009) EphA4 and EfnB2a maintain rhombomere coherence by independently regulating intercalation of progenitor cells in the zebrafish neural keel. Dev Biol 327:313-26

Showing the most recent 10 out of 25 publications