Formation of embryonic mesoderm is a critical early step in vertebrate embryogenesis. Nodal members of the TGFfi family of signaling factors are essential for mesoderm formation and a variety of other developmental processes. Given these diverse developmental functions and the ability of Nodal to reinforce its own expression by positive feedback, precise control of Nodal signaling is essential for normal development. To restrict Nodal activity, multiple antagonists of the Nodal pathway are expressed in the vertebrate embryo. A central goal of this proposal is to define the mechanisms that modulate Nodal pathway function to establish the spatial organization of the embryonic mesoderm. We have identified novel functions for two Fox family genes in regulating the Nodal signaling pathway during Xenopus mesodermal development. FoxDS functions in the Spemann organizer to repress negative regulators of Nodal expression and promote mesoderm formation. Fasti (FoxH1), a transcriptional mediator of Nodal signals, unexpectedly binds to Groucho corepressors to inhibit Nodal mesoderm induction and autoregulation. This suggests a role for Fasti-Groucho4 in silencing the Nodal pathway outside of the mesodermal domain. To determine how FoxD3 and Fasti modulate the Nodal pathway three Aims are proposed: 1) developmentally important targets of FoxDS will be identified by analysis of microarray screen candidates, and by defining factors that mediate the Nodal transcriptional response to FoxDS and 2) the Fasti-Groucho4 complex will be analyzed biochemically, transcriptionally, and developmentally to determine its role in mesoderm formation and Nodal pathway regulation. These studies will elucidate conserved mechanisms of vertebrate embryogenesis, and define a transcriptional network for the Nodal pathway that may reveal general mechanisms for regulating other TGFfi signaling pathways. FoxDS also maintains pluripotency of stem cell lineages, and the proposed mechanistic studies may contribute to a better understanding of stem cell biology. Furthermore, given the role of FoxDS in neural crest development and disease, and the potential role of Fasti-Groucho in modulating proliferative control by TGFIi signals, these studies also have significance for understanding human diseases of the neural crest and cancer.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
3R01GM064768-05A1S1
Application #
7465938
Study Section
Development - 1 Study Section (DEV1)
Program Officer
Haynes, Susan R
Project Start
2002-01-01
Project End
2011-04-30
Budget Start
2007-05-01
Budget End
2008-04-30
Support Year
5
Fiscal Year
2007
Total Cost
$49,623
Indirect Cost
Name
University of Pennsylvania
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
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Reid, Christine D; Zhang, Yan; Sheets, Michael D et al. (2012) Transcriptional integration of Wnt and Nodal pathways in establishment of the Spemann organizer. Dev Biol 368:231-41
Bae, Sangwoo; Reid, Christine D; Kessler, Daniel S (2011) Siamois and Twin are redundant and essential in formation of the Spemann organizer. Dev Biol 352:367-81
Chang, Lisa L; Kessler, Daniel S (2010) Foxd3 is an essential Nodal-dependent regulator of zebrafish dorsal mesoderm development. Dev Biol 342:39-50
Blythe, Shelby A; Reid, Christine D; Kessler, Daniel S et al. (2009) Chromatin immunoprecipitation in early Xenopus laevis embryos. Dev Dyn 238:1422-32
Yaklichkin, Sergey; Steiner, Aaron B; Lu, Qun et al. (2007) FoxD3 and Grg4 physically interact to repress transcription and induce mesoderm in Xenopus. J Biol Chem 282:2548-57
Yaklichkin, Sergey; Vekker, Alexander; Stayrook, Steven et al. (2007) Prevalence of the EH1 Groucho interaction motif in the metazoan Fox family of transcriptional regulators. BMC Genomics 8:201
Steiner, Aaron B; Engleka, Mark J; Lu, Qun et al. (2006) FoxD3 regulation of Nodal in the Spemann organizer is essential for Xenopus dorsal mesoderm development. Development 133:4827-38
Hanna, Lynn A; Foreman, Ruth K; Tarasenko, Illya A et al. (2002) Requirement for Foxd3 in maintaining pluripotent cells of the early mouse embryo. Genes Dev 16:2650-61