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A combinatorial enhancer recognized by Mad TCF and Brinker first activates then represses dpp expression in the posterior spiracles of Drosophila

机译:由MadTCF和Brinker识别的组合增强剂首先激活然后抑制果蝇后气门中的dpp表达

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摘要

A previous genetic analysis of a reporter gene carrying a 375bp region from a dpp intron (dppMX-lacZ) revealed that the Wingless and Dpp pathways are required to activate dpp expression in posterior spiracle formation. Here we report that within the dppMX region there is an enhancer with binding sites for TCF and Mad that are essential for activating dppMX expression in posterior spiracles. There is also a binding site for Brinker likely employed to repress dppMX expression. This combinatorial enhancer may be the first identified with the ability to integrate temporally distinct positive (TCF and Mad) and negative (Brinker) inputs in the same cells. Cuticle studies on a unique dpp mutant lacking this enhancer showed that it is required for viability and that the Filzkorper are U-shaped rather than straight. Together with gene expression data from these mutants and from brk mutants, our results suggest that there are two rounds of Dpp signaling in posterior spiracle development. The first round is associated with dorsal-ventral patterning and is necessary for designating the posterior spiracle field. The second is governed by the combinatorial enhancer and begins during germ band retraction. The second round appears necessary for proper spiracle internal morphology and fusion with the remainder of the tracheal system. Intriguingly, several aspects of dpp posterior spiracle expression and function are similar to demonstrated roles for Wnt and BMP signaling in proximal-distal outgrowth of the mammalian embryonic lung.
机译:先前对来自dpp内含子(dppMX-lacZ)的375bp区域的报道基因进行的遗传分析表明,需要Wingless和Dpp途径来激活后鼻孔形成中的dpp表达。在这里我们报告说,在dppMX区域内,存在一个具有TCF和Mad结合位点的增强子,这对于激活后气孔中的dppMX表达是必不可少的。 Brinker还有一个结合位点,可能用于抑制dppMX表达。这种组合增强子可能是第一个具有在同一单元格中整合时间上不同的正输入(TCF和Mad)和负输入(Brinker)的能力的。对缺少该增强子的独特dpp突变体的表皮研究表明,它是生存力所必需的,并且Filzkorper是U形而不是直形。连同来自这些突变体和brk突变体的基因表达数据,我们的结果表明在后气孔发育中有两轮Dpp信号传导。第一轮与背腹模式有关,是指定后椎间隙的必要条件。第二种是由组合增强剂控制的,并且在细菌带回缩期间开始。第二轮似乎是适当的气门内部形态和与气管系统其余部分融合的必要条件。有趣的是,dpp后气门的表达和功能的几个方面与已证明的Wnt和BMP信号在哺乳动物胚胎肺近端-远端生长中的作用相似。

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