Alifragis P, Poortinga G, Parkhurst S M, Delidakis C
Institute of Molecular Biology and Biotechnology, Foundation for Research and Technology, Hellas, and Department of Biology, University of Crete, Heraklion, Greece.
Proc Natl Acad Sci U S A. 1997 Nov 25;94(24):13099-104. doi: 10.1073/pnas.94.24.13099.
Neural fate specification in Drosophila is promoted by the products of the proneural genes, such as those of the achaete-scute complex, and antagonized by the products of the Enhancer of split [E(spl)] complex, hairy, and extramacrochaetae. As all these proteins bear a helix-loop-helix (HLH) dimerization domain, we investigated their potential pairwise interactions using the yeast two-hybrid system. The fidelity of the system was established by its ability to closely reproduce the already documented interactions among Da, Ac, Sc, and Extramacrochaetae. We show that the seven E(spl) basic HLH proteins can form homo- and heterodimers inter-se with distinct preferences. We further show that a subset of E(spl) proteins can heterodimerize with Da, another subset can heterodimerize with proneural proteins, and yet another with both, indicating specialization within the E(spl) family. Hairy displays no interactions with any of the HLH proteins tested. It does interact with the non-HLH protein Groucho, which itself interacts with all E(spl) basic HLH proteins, but with none of the proneural proteins or Da. We investigated the structural requirements for some of these interactions by site-specific and deletion mutagenesis.
果蝇中的神经命运特化由原神经基因的产物促进,如无刚毛 - 缺刻复合体的那些基因,并且受到分裂增强子[E(spl)]复合体、毛状基因和超大刚毛基因产物的拮抗。由于所有这些蛋白质都带有一个螺旋 - 环 - 螺旋(HLH)二聚化结构域,我们使用酵母双杂交系统研究了它们潜在的两两相互作用。该系统的保真度通过其紧密重现已记录的Da、Ac、Sc和超大刚毛基因之间相互作用的能力得以确立。我们表明,七种E(spl)碱性HLH蛋白可以相互形成同二聚体和异二聚体,且具有不同的偏好。我们进一步表明,一部分E(spl)蛋白可以与Da异二聚化,另一部分可以与原神经蛋白异二聚化,还有一部分可以与两者都异二聚化,这表明E(spl)家族内部存在特异性。毛状基因与所测试的任何HLH蛋白都没有相互作用。它确实与非HLH蛋白毛状体相互作用,而毛状体本身与所有E(spl)碱性HLH蛋白相互作用,但与任何原神经蛋白或Da都不相互作用。我们通过位点特异性和缺失诱变研究了其中一些相互作用的结构要求。