Lightfoot K, Duarte R, Segev O
Int J Oncol. 1995 Nov;7(5):1193-201. doi: 10.3892/ijo.7.5.1193.
The Drosophila ras2 promoter is an authentic bidirectional promoter governing the expression of both the Dras2 and rop genes by a single mechanism. Characterisation of the Dras2/rop promoter has revealed that a unitary complex (M) interacts with two promoter sub-domains (regions A and B). Two distinct transcription factors (factors A and B),which make up the major complex (M), bind regions A and B, respectively. We have analyzed the putative CACCC element and AP-1-Iike sequence contained within region B (-41 to -20) of the Dras2/rop promoter. It was found that AP-1 is not involved in Dras2 expression as is the case for the human Ha-ras1 gene. The entire CACCC motif (-34 to -21) shares 83% homology with the conserved mammalian element. Detailed mutational analysis has however revealed that the CACCC core sequence (-27 to -23) is vital for Dras2/rop recognition by factor B. The cytosine residues at positions -27, -25, -24 and -23 were observed to play a critical role in factor B recognition. Factor B has been purified as a 43 kD polypeptide as measured by SDS-PAGE and the relative mass was confirmed by photo-chemical crosslinking. Our findings are the first report of the conservation of the mammalian CACCC motif in Drosophila.
果蝇ras2启动子是一个真正的双向启动子,通过单一机制调控Dras2和rop基因的表达。对Dras2/rop启动子的表征显示,一个单一复合物(M)与两个启动子亚结构域(区域A和B)相互作用。构成主要复合物(M)的两种不同转录因子(因子A和因子B)分别结合区域A和B。我们分析了Dras2/rop启动子区域B(-41至-20)中包含的假定CACCC元件和类AP-1序列。结果发现,与人类Ha-ras1基因的情况不同,AP-1不参与Dras2的表达。整个CACCC基序(-34至-21)与保守的哺乳动物元件具有83%的同源性。然而,详细的突变分析表明,CACCC核心序列(-27至-23)对于因子B识别Dras2/rop至关重要。观察到-27、-25、-24和-23位的胞嘧啶残基在因子B识别中起关键作用。通过SDS-PAGE测定,因子B已被纯化,为一种43 kD的多肽,其相对分子量通过光化学交联得到证实。我们的发现是关于果蝇中哺乳动物CACCC基序保守性的首次报道。