Andrioli Luiz Paulo Moura, Vasisht Vikram, Theodosopoulou Ekaterina, Oberstein Adam, Small Stephen
Department of Biology, New York University, 1009 Main Building, 100 Washington Square East, New York 10003-6688, USA.
Development. 2002 Nov;129(21):4931-40. doi: 10.1242/dev.129.21.4931.
The striped expression pattern of the pair-rule gene even skipped (eve) is established by five stripe-specific enhancers, each of which responds in a unique way to gradients of positional information in the early Drosophila embryo. The enhancer for eve stripe 2 (eve 2) is directly activated by the morphogens Bicoid (Bcd) and Hunchback (Hb). As these proteins are distributed throughout the anterior half of the embryo, formation of a single stripe requires that enhancer activation is prevented in all nuclei anterior to the stripe 2 position. The gap gene giant (gt) is involved in a repression mechanism that sets the anterior stripe border, but genetic removal of gt (or deletion of Gt-binding sites) causes stripe expansion only in the anterior subregion that lies adjacent to the stripe border. We identify a well-conserved sequence repeat, (GTTT)(4), which is required for repression in a more anterior subregion. This site is bound specifically by Sloppy-paired 1 (Slp1), which is expressed in a gap gene-like anterior domain. Ectopic Slp1 activity is sufficient for repression of stripe 2 of the endogenous eve gene, but is not required, suggesting that it is redundant with other anterior factors. Further genetic analysis suggests that the (GTTT)(4)-mediated mechanism is independent of the Gt-mediated mechanism that sets the anterior stripe border, and suggests that a third mechanism, downregulation of Bcd activity by Torso, prevents activation near the anterior tip. Thus, three distinct mechanisms are required for anterior repression of a single eve enhancer, each in a specific position. Ectopic Slp1 also represses eve stripes 1 and 3 to varying degrees, and the eve 1 and eve 3+7 enhancers each contain GTTT repeats similar to the site in the eve 2 enhancer. These results suggest a common mechanism for preventing anterior activation of three different eve enhancers.
配对规则基因“even skipped”(eve)的条纹表达模式由五个条纹特异性增强子建立,每个增强子对早期果蝇胚胎中位置信息的梯度以独特方式做出反应。eve条纹2(eve 2)的增强子直接由形态发生素双胸(Bcd)和驼背(Hb)激活。由于这些蛋白质分布在胚胎前半部分,形成单一条纹需要防止条纹2位置前方所有细胞核中的增强子激活。间隙基因“giant”(gt)参与设定条纹前边界的抑制机制,但基因去除gt(或删除Gt结合位点)仅导致条纹在与条纹边界相邻的前亚区域扩展。我们鉴定出一个保守性良好的序列重复(GTTT)⁴,它是在前一个更靠前的亚区域进行抑制所必需的。这个位点特异性地结合松散配对1(Slp1),Slp1在类似间隙基因的前结构域中表达。异位Slp1活性足以抑制内源性eve基因的条纹2,但并非必需,这表明它与其他前部因子功能冗余。进一步的遗传分析表明,(GTTT)⁴介导的机制独立于设定条纹前边界的Gt介导的机制,并且表明第三种机制,即躯干蛋白(Torso)下调Bcd活性,可防止在前部顶端附近激活。因此,单个eve增强子的前部抑制需要三种不同机制,每种机制处于特定位置。异位Slp1也不同程度地抑制eve条纹1和3,并且eve 1和eve 3 + 7增强子各自包含与eve 2增强子中的位点相似的GTTT重复序列。这些结果表明存在一种防止三种不同eve增强子前部激活的共同机制。