Cited by 71Developmental Biology and Gene RegulationWnt/β-catenin signaling in development and cancerPluripotent Stem Cells Research

Global analysis of the transcriptional network controlling Xenopus endoderm formation

Sinner, Débora, Kirilenko, Pavel, Rankin, Scott, Wei, Eric, Howard, Laura, Kofron, Matthew, Heasman, Janet, Woodland, Hugh R. +1 more·2006·Development

Abstract

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.

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Crossref · 10.1242/dev.02358

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Authors
Sinner, D., Kirilenko, P., Rankin, S., Wei, E., Howard, L., Kofron, M., Heasman, J., Woodland, H. R., & Zorn, A. M.
Affiliations
  • Division of Developmental Biology, Cincinnati Children's Hospital Research Foundation and Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH 45299, USA.
  • University of Warwick (GB)
  • Cincinnati Children's Hospital Medical Center (US)
Venue
Development
Published
2006-05-15
Volume
133
Issue
10
Pages
1955-1966
ISSN
  • 0950-1991 (ISSN-L)
  • 1477-9129
OpenAlex
W2164498165
Cited by
71
References
0
Citations by year
2025: 1 · 2023: 1 · 2022: 2 · 2021: 2 · 2020: 4 · 2019: 4 · 2017: 1 · 2016: 4 · 2015: 2 · 2014: 6 · 2013: 1 · 2012: 4
FWCI
4.07
Type
journal article
Language
en
Open access
closed
Locations
  • Development (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Wellcome Trust
  • National Institute of Diabetes and Digestive and Kidney Diseases (R24DK064403, DK064403)
  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (R01HD033002, HD42572, R01HD042572, HD33002)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Wnt/β-catenin signaling in development and cancer
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Pluripotent Stem Cells Research
Keywords
endoderm formation, gene regulatory networks, Xenopus gastrula, Nodal signaling, mixer, SOX17, autoregulatory loop, transcriptional regulation, endoderm specification
MeSH terms
Animals, Embryo, Nonmammalian, Endoderm, Gastrula, Microinjections, Organ Culture Techniques, Transcription Factors, Transcription, Genetic, Xenopus, Oligonucleotides, Antisense, In Situ Hybridization, Gene Expression Regulation, Developmental, Reverse Transcriptase Polymerase Chain Reaction, Oligonucleotide Array Sequence Analysis, Xenopus Proteins

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