Allen A M, Anreiter I, Vesterberg A, Douglas S J, Sokolowski M B
a Department of Cell and Systems Biology , University of Toronto , Toronto , Canada.
b Department of Ecology and Evolutionary Biology , University of Toronto , Toronto , Canada.
J Neurogenet. 2018 Sep;32(3):256-266. doi: 10.1080/01677063.2018.1500572. Epub 2018 Oct 10.
Little is known about the molecular underpinning of behavioral pleiotropy. The Drosophila melanogaster foraging gene is highly pleiotropic, affecting many independent larval and adult phenotypes. Included in foraging's multiple phenotypes are larval foraging path length, triglyceride levels, and food intake. foraging has a complex structure with four promoters and 21 transcripts that encode nine protein isoforms of a cGMP dependent protein kinase (PKG). We examined if foraging's complex molecular structure underlies the behavioral pleiotropy associated with this gene. Using a promotor analysis strategy, we cloned DNA fragments upstream of each of foraging's transcription start sites and generated four separate for-Gal4s. Supporting our hypothesis of modular function, they had discrete, restricted expression patterns throughout the larva. In the CNS, for-Gal4 and for-Gal4 were expressed in neurons while for-Gal4 and for-Gal4 were expressed in glia cells. In the gastric system, for-Gal4 and for-Gal4 were expressed in enteroendocrine cells of the midgut while for-Gal4 was expressed in the stem cells of the midgut. for-Gal4 was expressed in the midgut enterocytes, and midgut and hindgut visceral muscle. for-Gal4's gastric system expression was restricted to the hindgut. We also found promoter specific expression in the larval fat body, salivary glands, and body muscle. The modularity of foraging's molecular structure was also apparent in the phenotypic rescues. We rescued larval path length, triglyceride levels (bordered on significance), and food intake of for null larvae using different for-Gal4s to drive UAS-for. In a foraging null genetic background, for-Gal4 was the only promoter driven Gal4 to rescue larval path length, for-Gal4 altered triglyceride levels, and for-Gal4 rescued food intake. Our results refine the spatial expression responsible for foraging's associated phenotypes, as well as the sub-regions of the locus responsible for their expression. foraging's pleiotropy arises at least in part from the individual contributions of its four promoters.
关于行为多效性的分子基础,我们知之甚少。果蝇的觅食基因具有高度多效性,会影响许多独立的幼虫和成虫表型。觅食的多种表型包括幼虫觅食路径长度、甘油三酯水平和食物摄入量。觅食基因具有复杂的结构,有四个启动子和21个转录本,可编码一种环鸟苷酸依赖性蛋白激酶(PKG)的九种蛋白质异构体。我们研究了觅食基因复杂的分子结构是否是与该基因相关的行为多效性的基础。使用启动子分析策略,我们克隆了觅食基因每个转录起始位点上游的DNA片段,并生成了四个独立的for-Gal4。支持我们关于模块化功能的假设,它们在整个幼虫中具有离散、受限的表达模式。在中枢神经系统中,for-Gal4和for-Gal4在神经元中表达,而for-Gal4和for-Gal4在神经胶质细胞中表达。在胃系统中,for-Gal4和for-Gal4在中肠的肠内分泌细胞中表达,而for-Gal4在中肠的干细胞中表达。for-Gal4在中肠肠上皮细胞、中肠和后肠内脏肌肉中表达。for-Gal4在胃系统中的表达仅限于后肠。我们还在幼虫脂肪体、唾液腺和身体肌肉中发现了启动子特异性表达。觅食基因分子结构的模块化在表型拯救中也很明显。我们使用不同的for-Gal4驱动UAS-for,拯救了觅食基因缺失幼虫的幼虫路径长度、甘油三酯水平(接近显著水平)和食物摄入量。在觅食基因缺失的遗传背景下,for-Gal4是唯一能拯救幼虫路径长度的启动子驱动的Gal4,for-Gal4改变了甘油三酯水平,for-Gal4拯救了食物摄入量。我们的结果细化了负责觅食相关表型的空间表达,以及负责其表达的基因座子区域。觅食基因的多效性至少部分源于其四个启动子的个体贡献。