New roles for FoxH1 in patterning the early embryo

FoxH1 (Fast1) was first characterized as the transcriptional partner for Smad proteins. Together with Smad2/4, it forms the activin response factor (ARF) that binds to the Mix.2 promoter in Xenopus embryos. Foxh1 is expressed maternally in Xenopus . Depletion of maternal Foxh1 mRNA results in abnorm...

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Veröffentlicht in:Development (Cambridge) 2004-10, Vol.131 (20), p.5065-5078
Hauptverfasser: Kofron, Matt, Puck, Helbert, Standley, Henrietta, Wylie, Chris, Old, Robert, Whitman, Malcolm, Heasman, Janet
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Sprache:eng
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Zusammenfassung:FoxH1 (Fast1) was first characterized as the transcriptional partner for Smad proteins. Together with Smad2/4, it forms the activin response factor (ARF) that binds to the Mix.2 promoter in Xenopus embryos. Foxh1 is expressed maternally in Xenopus . Depletion of maternal Foxh1 mRNA results in abnormalities of head and dorsal axis formation. We show that FoxH1 is required, together with XTcf3/β catenin, to activate the zygotic expression of the nodal gene, Xnr3 in a Smad2-independent manner. In contrast, maternal FoxH1 acts as an inhibitor of Xnr5 and 6 transcription, preventing their upregulation on the ventral side of the embryo, by the maternal T-box transcription factor VegT. We conclude that maternal FoxH1 has essential, context-dependent roles in regulating the pattern of zygotic gene expression in the early embryo.
ISSN:0950-1991
1477-9129
DOI:10.1242/dev.01396