Ring Colleen, Ogata Souichi, Meek Lauren, Song Jihwan, Ohta Tatsuru, Miyazono Kohei, Cho Ken W Y
Department of Developmental and Cell Biology, and Developmental Biology Center, University of California, Irvine, California 92697-2300, USA.
Genes Dev. 2002 Apr 1;16(7):820-35. doi: 10.1101/gad.963802.
We investigated the regulation of the activin/nodal-inducible distal element (DE) of the Xenopus goosecoid (gsc) promoter. On the basis of its interaction with the DE, we isolated a Xenopus homolog of the human Williams-Beuren syndrome critical region 11 (XWBSCR11), and further, show that it interacts with pathway-specific Smad2 and Smad3 in a ligand-dependent manner. Interestingly, we also find that XWBSCR11 functions cooperatively with FoxH1 (Fast-1) to stimulate DE-dependent transcription. We propose a mechanism in which FoxH1 functions together with Smads as a cofactor for the recruitment of transcription factors like XWBSCR11 in the process of activin/nodal-mediated gsc-specific induction. This mechanism provides considerable opportunities for modulation of transcription across a variety of activin/nodal-inducible genes, increasing diversity in promoter selection, thus leading to the differential induction of activin/nodal target genes.
我们研究了非洲爪蟾鹅膏蕈氨酸(gsc)启动子的激活素/节点诱导远端元件(DE)的调控机制。基于其与DE的相互作用,我们分离出了人类威廉姆斯-博伦综合征关键区域11(XWBSCR11)的非洲爪蟾同源物,并进一步表明它以配体依赖的方式与特定途径的Smad2和Smad3相互作用。有趣的是,我们还发现XWBSCR11与FoxH1(Fast-1)协同作用以刺激DE依赖的转录。我们提出了一种机制,即在激活素/节点介导的gsc特异性诱导过程中,FoxH1与Smads一起作为辅助因子,用于招募像XWBSCR11这样的转录因子。这种机制为调控多种激活素/节点诱导基因的转录提供了大量机会,增加了启动子选择的多样性,从而导致激活素/节点靶基因的差异诱导。