Jennings B H, Tyler D M, Bray S J
Department of Anatomy, University of Cambridge, Cambridge CB2 3DY, United Kingdom.
Mol Cell Biol. 1999 Jul;19(7):4600-10. doi: 10.1128/MCB.19.7.4600.
Seven Enhancer of split genes in Drosophila melanogaster encode basic-helix-loop-helix transcription factors which are components of the Notch signalling pathway. They are expressed in response to Notch activation and mediate some effects of the pathway by regulating the expression of target genes. Here we have determined that the optimal DNA binding site for the Enhancer of split proteins is a palindromic 12-bp sequence, 5'-TGGCACGTG(C/T)(C/T)A-3', which contains an E-box core (CACGTG). This site is recognized by all of the individual Enhancer of split basic helix-loop-helix proteins, consistent with their ability to regulate similar target genes in vivo. We demonstrate that the 3 bp flanking the E-box core are intrinsic to DNA recognition by these proteins and that the Enhancer of split and proneural proteins can compete for binding on specific DNA sequences. Furthermore, the regulation conferred on a reporter gene in Drosophila by three closely related sequences demonstrates that even subtle sequence changes within an E box or flanking bases have dramatic consequences on the overall repertoire of proteins that can bind in vivo.
果蝇中的七个分裂增强子基因编码碱性螺旋-环-螺旋转录因子,它们是Notch信号通路的组成部分。它们在Notch激活时表达,并通过调节靶基因的表达介导该通路的一些效应。我们在此确定,分裂增强子蛋白的最佳DNA结合位点是一个回文12碱基序列,5'-TGGCACGTG(C/T)(C/T)A-3',其中包含一个E-box核心(CACGTG)。所有单个的分裂增强子碱性螺旋-环-螺旋蛋白都能识别该位点,这与其在体内调节相似靶基因的能力一致。我们证明,E-box核心两侧的3个碱基对于这些蛋白识别DNA至关重要,并且分裂增强子蛋白和原神经蛋白能够竞争结合特定的DNA序列。此外,三个密切相关序列对果蝇中报告基因的调控表明,即使E-box或侧翼碱基内的细微序列变化也会对体内能够结合的蛋白总体库产生显著影响。