The focus of research in the three laboratories that constitute this Program Project is the molecular basis of regulatory flow in early embryonic development. The Program Project will utilize the highly developed sea urchin and ascidian model systems for this research. Major objective are to develop functional comprehension of cis-regulatory systems that control genes expressed spatially in the early embryo, using genes that operate at different levels of the gene regulatory network; to discern the overall architecture of this network; and to discern the molecular mechanisms by which maternal transcription factors are activated, and control is transformed from maternal to zygotic regulatory processes. The three Research Components are:(1) Davidson Component, """"""""Gene Regulatory Mechanisms and the Control of Early Embryogenesis""""""""; (2) Fraser Component, """"""""In Vivo Imaging of Gene Regulatory Events in the Early Embryo""""""""; (3) Levine Component """"""""Gene Regulation in the Ascidian Ciona intestinalis."""""""" The major aims of the Davidson Component are cis-regulatory analysis of genes expressed differentially in the sea urchin embryo, and identification and characterization of the maternal and zygotic transcription factors which control this expression. The major focus of the Fraser Component is visualization of the state of cis-regulatory elements in vivo and spatial visualization by new imaging methods of modifications of maternal transcription factors, using experimental systems characterized in the Davidson Component. The major focus of the Levine Component will be cis-regulatory analysis of certain key regulatory genes expressed in ascidian embryos, which are also to be characterized in the sea urchin embryo in the Davidson Component, and interphyletic gene transfer experiments to be carried out collaboratively between the Davidson and Levine labs. A salient characteristic of the proposed research is the engagement of powerful new technologies, some entirely novel. All the Components. Will rely on two Research Core Facilities, viz the SUMS Facility at Caltech's Marine Laboratory, which will provide sea urchins, gametes and nuclear extracts from which transcription factors are purified; and the Microsequencing Facility, where partially purified transcription factors are sequenced at picomole levels. An Administrative Core will oversee management, budget, and interlaboratory communication, with respect to material, financial, and intellectual matters.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Program Projects (P01)
Project #
1P01HD037105-01
Application #
2739292
Study Section
Special Emphasis Panel (ZHD1-DRG-D (H))
Program Officer
Tasca, Richard J
Project Start
1999-04-01
Project End
2004-03-31
Budget Start
1999-04-01
Budget End
2000-03-31
Support Year
1
Fiscal Year
1999
Total Cost
Indirect Cost
Name
California Institute of Technology
Department
Type
Schools of Arts and Sciences
DUNS #
078731668
City
Pasadena
State
CA
Country
United States
Zip Code
91125
Slota, Leslie A; McClay, David R (2018) Identification of neural transcription factors required for the differentiation of three neuronal subtypes in the sea urchin embryo. Dev Biol 435:138-149
Hutchins, Erica J; Kunttas, Ezgi; Piacentino, Michael L et al. (2018) Migration and diversification of the vagal neural crest. Dev Biol :
Kerosuo, Laura; Neppala, Pushpa; Hsin, Jenny et al. (2018) Enhanced expression of MycN/CIP2A drives neural crest toward a neural stem cell-like fate: Implications for priming of neuroblastoma. Proc Natl Acad Sci U S A 115:E7351-E7360
Rogers, Crystal D; Sorrells, Lisa K; Bronner, Marianne E (2018) A catenin-dependent balance between N-cadherin and E-cadherin controls neuroectodermal cell fate choices. Mech Dev 152:44-56
McClay, David R; Miranda, Esther; Feinberg, Stacy L (2018) Neurogenesis in the sea urchin embryo is initiated uniquely in three domains. Development 145:
Roellig, Daniela; Tan-Cabugao, Johanna; Esaian, Sevan et al. (2017) Dynamic transcriptional signature and cell fate analysis reveals plasticity of individual neural plate border cells. Elife 6:
Lignell, Antti; Kerosuo, Laura; Streichan, Sebastian J et al. (2017) Identification of a neural crest stem cell niche by Spatial Genomic Analysis. Nat Commun 8:1830
Martik, Megan L; McClay, David R (2017) New insights from a high-resolution look at gastrulation in the sea urchin, Lytechinus variegatus. Mech Dev 148:3-10
Murko, Christina; Bronner, Marianne E (2017) Tissue specific regulation of the chick Sox10E1 enhancer by different Sox family members. Dev Biol 422:47-57
Peter, Isabelle S (2017) Regulatory states in the developmental control of gene expression. Brief Funct Genomics 16:281-287

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