TGFβ and BMP-2 activation of the OPN promoter:: Roles of Smad- and Hox-binding elements

被引:97
作者
Hullinger, TG
Pan, Q
Viswanathan, HL
Somerman, MJ
机构
[1] Univ Michigan, Sch Dent, Dept Pharmacol, Ann Arbor, MI 48109 USA
[2] Pfizer Inc, Cardiovasc Therapeut, Ann Arbor, MI 48105 USA
[3] Univ Michigan, Sch Dent, Dept Periodont Prevent Geriatr, Ann Arbor, MI 48109 USA
关键词
D O I
10.1006/excr.2000.5074
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Members of the transforming growth factor superfamily are known to transduce signals via the activation of Smad proteins. Ligand binding to transmembrane cell surface receptors triggers the phosphorylation of pathway-specific Smads. These Smads then complex with Smad 4 and are translocated to the nucleus where they effect gene transcription. Smads 1 and 4 were recently demonstrated to mediate BMP activation of the OPN promoter by inhibiting the interaction of Hoxc-8 protein with a Hox-binding element. While previous studies have indicated that specific DNA sequences are recognized by Smad complexes in several promoters, the role of Smad-binding elements (SBEs) in activation of the OPN promoter by members of the TGF beta superfamily has not been previously evaluated. In this study we tested the hypothesis that a putative Smad-binding region containing the sequence AGACTGTCTGGAC is involved in the activation of the OPN promoter by members of the TGF beta superfamily. Functional analyses demonstrated that the both the HBE- and Smad-binding region were involved in BMP-2-induced activation of the promoter, whereas, the HBE appeared to be the primary region involved in activation by TGF beta. Deletion of the first 9 bases in the Smad-binding region substantially reduced BMP-a-mediated activation of the promoter. These results strongly suggest that both the Hox- and the Smad-binding regions play a role in BMP-2-induced activation of the OPN promoter. (C) 2001 Academic Press.
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页码:69 / 74
页数:6
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