Smad3-Smad4 and AP-1 Complexes Synergize in Transcriptional Activation of the c-Jun Promoter by Transforming Growth Factor β

Author:

Wong Carolyn1,Rougier-Chapman Elissa M.1,Frederick Joshua P.1,Datto Michael B.1,Liberati Nicole T.1,Li Jian-Ming2,Wang Xiao-Fan1

Affiliation:

1. Department of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, North Carolina 27708, 1 and

2. Division of Basic Sciences, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 208922

Abstract

ABSTRACT Transcriptional regulation by transforming growth factor β (TGF-β) is a complex process which is likely to involve cross talk between different DNA responsive elements and transcription factors to achieve maximal promoter activation and specificity. Here, we describe a concurrent requirement for two discrete responsive elements in the regulation of the c-Jun promoter, one a binding site for a Smad3-Smad4 complex and the other an AP-1 binding site. The two elements are located 120 bp apart in the proximal c-Jun promoter, and each was able to independently bind its corresponding transcription factor complex. The effects of independently mutating each of these elements were nonadditive; disruption of either sequence resulted in complete or severe reductions in TGF-β responsiveness. This simultaneous requirement for two distinct and independent DNA binding elements suggests that Smad and AP-1 complexes function synergistically to mediate TGF-β-induced transcriptional activation of the c-Jun promoter.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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