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首页> 外文期刊>G3: Genes, Genomes, Genetics >A Flippase-Mediated GAL80/GAL4 Intersectional Resource for Dissecting Appendage Development in Drosophila
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A Flippase-Mediated GAL80/GAL4 Intersectional Resource for Dissecting Appendage Development in Drosophila

机译:Flippase介导的GAL80 / GAL4交叉资源,用于解剖果蝇的附件发育。

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摘要

Drosophila imaginal discs provide an ideal model to study processes important for cell signaling and cell specification, tissue differentiation, and cell competition during development. One challenge to understanding genetic control of cellular processes and cell interactions is the difficulty in effectively targeting a defined subset of cells in developing tissues in gene manipulation experiments. A recently developed Flippase-induced intersectional GAL80/GAL4 repression method incorporates several gene manipulation technologies in Drosophila to enable such fine-scale dissection in neural tissues. In particular, this approach brings together existing GAL4 transgenes, newly developed enhancer-trap flippase transgenes, and GAL80 transgenes flanked by Flippase recognition target sites. The combination of these tools enables gene activation/repression in particular subsets of cells within a GAL4 expression pattern. Here, we expand the utility of a large collection of these enhancer-trap flippase transgenic insertion lines by characterizing their expression patterns in third larval instar imaginal discs. We screened 521 different enhancer-trap flippase lines and identified 28 that are expressed in imaginal tissues, including two transgenes that show sex-specific expression patterns. Using a line that expresses Flippase in the wing imaginal disc, we demonstrate the utility of this intersectional approach for studying development by knocking down gene expression of a key member of the planar cell polarity pathway. The results of our experiments show that these enhancer-trap flippase lines enable fine-scale manipulation in imaginal discs.
机译:果蝇假想盘为研究在发育过程中对细胞信号传导和细胞规格,组织分化以及细胞竞争至关重要的过程提供了理想的模型。理解细胞过程和细胞相互作用的遗传控制的一个挑战是在基因操作实验中难以有效地靶向发育中的组织中定义的细胞子集。最近开发的Flippase诱导的相交GAL80 / GAL4抑制方法在果蝇中结合了几种基因操作技术,可在神经组织中进行这种精细的解剖。特别是,这种方法将现有的GAL4转基因,新开发的增强子诱集的flippase转基因和侧接Flippase识别靶位点的GAL80转基因结合在一起。这些工具的组合可在GAL4表达模式内的特定细胞亚群中实现基因激活/抑制。在这里,我们通过表征它们在第三龄幼虫假想盘中的表达模式,扩展了这些增强子捕获翻转酶转基因插入系的大量收集。我们筛选了521种不同的增强子捕获翻转酶系,并鉴定了在假体组织中表达的28种,包括两个显示性别特异性表达模式的转基因。使用在机翼假想盘中表达Flippase的线,我们通过敲低平面细胞极性途径关键成员的基因表达,证明了这种交叉方法在研究发育中的效用。我们的实验结果表明,这些增强子捕获的翻转酶谱系能够在假想椎间盘中进行精细操作。

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