Ma X, Yuan D, Scarborough T, Ma J
Division of Developmental Biology, Children's Hospital Research Foundation, University of Cincinnati College of Medicine, 3333 Burnet Avenue, Cincinnati, OH 45229-3039, USA.
Biochem J. 1999 Mar 1;338 ( Pt 2)(Pt 2):447-55.
Bicoid is a Drosophila morphogenetic protein required for the development of anterior structures in the embryo. To gain a better understanding of how Bicoid works as a transcriptional activator, we systematically analysed various functions of Bicoid required for gene activation. We provide evidence suggesting that Bicoid is an intrinsically weak activator. First, our biochemical experiments demonstrate that the Bicoid-DNA complexes are very unstable, suggesting a weak DNA-binding function of Bicoid. This idea is further supported by our experiments demonstrating that the same number of LexA-Bicoid fusion molecules can activate transcription more effectively from LexA sites than from Bicoid sites. Secondly, we demonstrate that transcriptional activation by the weak activator Bicoid is readily influenced by the local enhancer environment. These influences are decreased when the Bicoid function is enforced by attaching to it either a known dimerization domain or the strong activation domain VP16. VP16 can also compensate for the loss of some Bicoid sites in an enhancer element. Our experiments demonstrate that the outcome of transcriptional activation by Bicoid is determined by multiple weak functions that are interconnected, a finding that can further help us to understand how this morphogenetic protein achieves its molecular functions.
双尾是果蝇胚胎中发育前体结构所需的一种形态发生蛋白。为了更好地理解双尾作为转录激活因子的作用机制,我们系统地分析了基因激活所需的双尾的各种功能。我们提供的证据表明双尾是一种内在的弱激活因子。首先,我们的生化实验表明双尾 - DNA复合物非常不稳定,这表明双尾的DNA结合功能较弱。我们的实验进一步支持了这一观点,即相同数量的LexA - 双尾融合分子从LexA位点比从双尾位点能更有效地激活转录。其次,我们证明了弱激活因子双尾的转录激活很容易受到局部增强子环境的影响。当通过连接已知的二聚化结构域或强激活结构域VP16来增强双尾功能时,这些影响会减弱。VP16还可以补偿增强子元件中一些双尾位点的缺失。我们的实验表明,双尾转录激活的结果是由多个相互关联的弱功能决定的,这一发现可以进一步帮助我们理解这种形态发生蛋白是如何实现其分子功能的。