Mauhin V, Lutz Y, Dennefeld C, Alberga A
Laboratoire de Génétique Moléculaire des Eucaryotes du CNRS, Unité 184 de Biologie Moléculaire et de Génie Génétique de l'INSERM, Faculté de Médecine, Strasbourg, France.
Nucleic Acids Res. 1993 Aug 25;21(17):3951-7. doi: 10.1093/nar/21.17.3951.
The Drosophila gene snail (sna) which encodes a zinc finger protein is essential for dorsal-ventral pattern formation in the developing embryo. We have defined a repertoire of SNAIL (SNA) binding sites using recombinant SNA proteins to select specific binding sequences from a pool of random sequence nucleotides. The bound sequences which were selected by multiple rounds of gel retardation and amplification by the polymerase chain reaction (PCR) were subsequently cloned and sequenced. The consensus sequence, 5'G/A A/t G/A A CAGGTG C/t A C 3', with a highly conserved core of 6 bases, CAGGTG, shares no significant homology with known binding sequences of other Drosophila zinc finger proteins. However, the CAGGTG core is identical to the core motif of aHLH (helix-loop-helix) binding sites. The strongest SNA binding is obtained with sequences containing this core motif whereas reduced binding is seen for sequences with canonical CANNTG HLH motifs. Interestingly, SNA binding is detected in the promoter region of the snail gene. Transient expression in co-transfection experiments using a SNA binding element (SBE) linked to a heterologous promoter indicates that SNA has the ability to function as a transcription activator.
果蝇的蜗牛基因(sna)编码一种锌指蛋白,对发育中胚胎的背腹模式形成至关重要。我们利用重组SNA蛋白从随机序列核苷酸池中选择特定结合序列,确定了一系列SNAIL(SNA)结合位点。通过多轮凝胶阻滞和聚合酶链反应(PCR)扩增选择出的结合序列随后被克隆并测序。共有序列5'G/A A/t G/A A CAGGTG C/t A C 3',具有高度保守的6碱基核心CAGGTG,与其他果蝇锌指蛋白的已知结合序列没有显著同源性。然而,CAGGTG核心与aHLH(螺旋-环-螺旋)结合位点的核心基序相同。含有该核心基序的序列能获得最强的SNA结合,而具有典型CANNTG HLH基序的序列结合力降低。有趣的是,在蜗牛基因的启动子区域检测到SNA结合。使用与异源启动子相连的SNA结合元件(SBE)进行共转染实验中的瞬时表达表明,SNA具有作为转录激活因子发挥作用的能力。