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First published online May 1, 2006
doi: 10.1242/10.1242/dev.02358


Development 133, 1955-1966 (2006)
Published by The Company of Biologists 2006


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Global analysis of the transcriptional network controlling Xenopus endoderm formation

Débora Sinner1, Pavel Kirilenko2, Scott Rankin1, Eric Wei1, Laura Howard2, Matthew Kofron1, Janet Heasman1, Hugh R. Woodland2,* and Aaron M. Zorn1,*

1 Division of Developmental Biology, Cincinnati Children's Hospital Research Foundation and Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH 45299, USA.
2 Department of Biological Sciences, University of Warwick, Coventry CV4 7AL, UK.

* Authors for correspondence (e-mail: h.r.woodland{at}warwick.ac.uk; aaron.zorn{at}chmcc.org)

Accepted 13 March 2006

A conserved molecular pathway has emerged controlling endoderm formation in Xenopus zebrafish and mice. Key genes in this pathway include Nodal ligands and transcription factors of the Mix-like paired homeodomain class, Gata4-6 zinc-finger factors and Sox17 HMG domain proteins. Although a linear epistatic pathway has been proposed, the precise hierarchical relationships between these factors and their downstream targets are largely unresolved. Here, we have used a combination of microarray analysis and loss-of-function experiments to examine the global regulatory network controlling Xenopus endoderm formation. We identified over 300 transcripts enriched in the gastrula endoderm, including most of the known endoderm regulators and over a hundred uncharacterized genes. Surprisingly only 10% of the endoderm transcriptome is regulated as predicted by the current linear model. We find that Nodal genes, Mixer and Sox17 have both shared and distinct sets of downstream targets, and that a number of unexpected autoregulatory loops exist between Sox17 and Gata4-6, between Sox17 and Bix1/Bix2/Bix4, and between Sox17 and Xnr4. Furthermore, we find that Mixer does not function primarily via Sox17 as previously proposed. These data provides new insight into the complexity of endoderm formation and will serve as valuable resource for establishing a complete endoderm gene regulatory network.

Key words: Endoderm, Development, Xenopus, Nodal, Sox17, Gata, Mixer, Microarray, Gene regulatory network


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© The Company of Biologists Ltd 2006