Abstract

Nodal and Smad2/3 signals play pivotal roles in mesendoderm induction and axis determination during late blastulation and early gastrulation in vertebrate embryos. However, Smad2/3 direct target genes during those critical developmental stages have not been systematically identified. Here, through ChIP-chip assay, we show that the promoter/enhancer regions of 679 genes are bound by Smad2 in the zebrafish early gastrulas. Expression analyses confirm that a significant proportion of Smad2 targets are indeed subjected to Nodal/Smad2 regulation at the onset of gastrulation. The co-existence of DNA-binding sites of other transcription factors in the Smad2-bound regions allows the identification of well known Smad2-binding partners, such as FoxH1 and Lef1/β-catenin, as well as many previously unknown Smad2 partners, including Oct1 and Gata6, during embryogenesis. We demonstrate that Oct1 physically associates with and enhances the transcription and mesendodermal induction activity of Smad2, whereas Gata6 exerts an inhibitory role in Smad2 signaling and mesendodermal induction. Thus, our study systemically uncovers a large number of Smad2 targets in early gastrulas and suggests cooperative roles of Smad2 and other transcription factors in controlling target gene transcription, which will be valuable for studying regulatory cascades during germ layer formation and patterning of vertebrate embryos.

Highlights

  • During early development of vertebrate embryos, signaling molecules play essential roles in axis determination and germ layer induction and patterning

  • Nodal signals are essential for mesendoderm induction during early development of vertebrate embryos

  • The genome-wide analyses of Smad2/3-binding sites in HaCaT keratinocytes and mouse ES cells are previously reported [68, 69], the mechanisms of Nodal signaling acting through Smad2/3 targets during early embryonic development remain largely unclear

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Summary

EXPERIMENTAL PROCEDURES

Fish Embryos—The Tuebingen line of zebrafish was used. Embryos were collected from natural matings, raised in Holtfreter’s solution at 28.5 °C, and staged by morphology as described previously [28]. The probes were re-mapped to the Zv7 genome, and only uniquemapped ones were retained, which represented promoter regions of 10,117 zebrafish genes. The 1000-bp sequences upstream of TSS of zebrafish Refseq mRNA were chosen as the control set To determine whether this motif is significantly enriched in foreground versus background, Z-score and p values were calculated as described previously [34, 35]. We investigated the emergence frequency of significantly enriched motifs in the 200-bp peaks containing the Smad2/4-binding motif. Site-specific PCR Analysis—To confirm the enrichment of selected Smad target sites, a subset of primers (see supplemental “Experimental Procedures” for details) corresponding to the predicted binding sites was designed to amplify a 200 –300-bp region around the peak probes. Each experiment was performed in triplicate, and the data represent the means Ϯ S.D. of three independent experiments after normalization to Renilla activity

RESULTS
Emergence frequency
DISCUSSION
Full Text
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