A network of interacting transcriptional regulators involved in Drosophila neural fate specification revealed by the yeast two-hybrid system

被引:67
作者
Alifragis, P
Poortinga, G
Parkhurst, SM
Delidakis, C
机构
[1] FDN RES & TECHNOL HELLAS, INST MOL BIOL & BIOTECHNOL, GR-71110 IRAKLION, GREECE
[2] UNIV CRETE, DEPT BIOL, GR-71110 IRAKLION, GREECE
[3] FRED HUTCHINSON CANC RES CTR, DIV BASIC SCI, SEATTLE, WA 98109 USA
关键词
D O I
10.1073/pnas.94.24.13099
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 home-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.
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页码:13099 / 13104
页数:6
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