Biozentrum der Universität Basel, Basel, Switzerland.
Nat Struct Mol Biol. 2010 Jan;17(1):69-76. doi: 10.1038/nsmb.1715. Epub 2009 Dec 13.
The transforming growth factor beta (TGF-beta) family member Decapentaplegic (Dpp) is a key regulator of patterning and growth in Drosophila development. Previous studies have identified a short DNA motif called the silencer element (SE), which recruits a trimeric Smad complex and the repressor Schnurri to downregulate target enhancers upon Dpp signaling. We have now isolated the minimal enhancer of the dad gene and discovered a short motif we termed the activating element (AE). The AE is similar to the SE and recruits the Smad proteins via a conserved mechanism. However, the AE and SE differ at important nucleotide positions. As a consequence, the AE does not recruit Schnurri but rather integrates repressive input by the default repressor Brinker and activating input by the Smad signal transducers Mothers against Dpp (Mad) and Medea via competitive DNA binding. The AE allows the identification of hitherto unknown direct Dpp targets and is functionally conserved in vertebrates.
转化生长因子β(TGF-β)家族成员 Decapentaplegic(Dpp)是果蝇发育中模式形成和生长的关键调节剂。先前的研究已经确定了一个短的 DNA 基序,称为沉默元件(SE),它招募三聚体 Smad 复合物和阻遏物 Schnurri,在 Dpp 信号转导时下调靶增强子。我们现在已经分离出 dad 基因的最小增强子,并发现了一个我们称之为激活元件(AE)的短基序。AE 类似于 SE,通过保守机制招募 Smad 蛋白。然而,AE 和 SE 在重要的核苷酸位置上有所不同。因此,AE 不招募 Schnurri,而是通过默认阻遏物 Brinker 的抑制性输入和 Smad 信号转导物 Mothers against Dpp(Mad)和 Medea 的激活输入通过竞争性 DNA 结合进行整合。AE 允许鉴定迄今未知的直接 Dpp 靶标,并在脊椎动物中具有功能保守性。