Hartman Institute for Therapeutic Organ Regeneration

An Oct-1 binding site mediates activation of the gata2 promoter by BMP signaling.

TitleAn Oct-1 binding site mediates activation of the gata2 promoter by BMP signaling.
Publication TypeJournal Article
Year of Publication2005
AuthorsOren T, Torregroza I, Evans T
JournalNucleic Acids Res
Volume33
Issue13
Pagination4357-67
Date Published2005
ISSN1362-4962
KeywordsAnimals, Binding Sites, Bone Morphogenetic Protein 4, Bone Morphogenetic Proteins, DNA-Binding Proteins, GATA2 Transcription Factor, Gene Expression Regulation, Developmental, Octamer Transcription Factor-1, Promoter Regions, Genetic, Response Elements, Sequence Deletion, Signal Transduction, Smad Proteins, Trans-Activators, Transcription Factors, Transcriptional Activation, Xenopus Proteins, Zebrafish, Zebrafish Proteins
Abstract

The gata2 gene encodes a transcription factor implicated in regulating early patterning of ectoderm and mesoderm, and later in numerous cell-specific gene expression programs. Activation of the gata2 gene during embryogenesis is dependent on the bone morphogenetic protein (BMP) signaling pathway, but the mechanism for how signaling controls gene activity has not been defined. We developed an assay in Xenopus embryos to analyze regulatory sequences of the zebrafish gata2 promoter that are necessary to mediate the response to BMP signaling during embryogenesis. We show that activation is Smad dependent, since it is blocked by expression of the inhibitory Smad6. Deletion analysis identified an octamer binding site that is necessary for BMP-mediated induction, and that interacts with the POU homeodomain protein Oct-1. However, this element is not sufficient to transfer a BMP response to a heterologous promoter, requiring an additional more proximal cooperating element. Based on recent studies with other BMP-dependent promoters (Drosophila vestigial and Xenopus Xvent-2), our studies of the gata2 gene suggest that POU-domain proteins comprise a common component of the BMP signaling pathway, cooperating with Smad proteins and other transcriptional activators.

DOI10.1093/nar/gki746
Alternate JournalNucleic Acids Res
PubMed ID16061939
PubMed Central IDPMC1182169
Grant ListR01 HL056182 / HL / NHLBI NIH HHS / United States
R37 HL056182 / HL / NHLBI NIH HHS / United States
HL056182 / HL / NHLBI NIH HHS / United States

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Hartman Institute for Therapeutic Organ Regeneration
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