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Smad1 and Smad4 are components of the bone morphogenetic protein-4 (BMP-4)-induced transcription complex of the Xvent-2B promoter
被引:71
作者:

Henningfeld, KA
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机构: Univ Ulm, Biochem Abt, D-89081 Ulm, Germany

Rastegar, S
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机构: Univ Ulm, Biochem Abt, D-89081 Ulm, Germany

Adler, G
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机构: Univ Ulm, Biochem Abt, D-89081 Ulm, Germany

Knöchel, W
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机构: Univ Ulm, Biochem Abt, D-89081 Ulm, Germany
机构:
[1] Univ Ulm, Biochem Abt, D-89081 Ulm, Germany
[2] Univ Ulm, Innere Med Abt 1, D-89081 Ulm, Germany
关键词:
D O I:
10.1074/jbc.M000978200
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
To study the mechanism of transcriptional activation of the Xenopus homeobox gene Xvent-2B, we have delineated the bone morphogenetic protein-4 (BMP-4)-responsive region between -275/-152 in the proximal pro meter. Consistent with the BMP-4 inductive nature of this region, this element exhibits transcriptional activation upon ectopic expression of Smad1 and Smad4. Electrophoretic mobility shift assays with total cellular extracts demonstrated that a DNA fragment encompassing this region was competent in the formation of a BMP-4-induced protein-DNA complex containing Smad1. Two different Smad binding regions were localized, a distal binding region for Smad1 containing two GCAT motifs and proximal AGNC binding sites for Smad4, the latter being conserved in other transforming growth factor-beta-responsive elements. Mutation of the Smad4 binding motif completely abolished transcriptional activation, whereas mutation or deletion of the Smad1 recognition sequence inhibited Smad1/Smad4 responsiveness. These results provide a functional characterization and identification of a vertebrate Smad1/Smad4 DNA response element induced by BMP-4 signaling and offers insight into the transcriptional regulation of a component essential for dorsoventral patterning in Xenopus embryos.
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页码:21827 / 21835
页数:9
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