Roark M, Raghavan K V, Todo T, Mayeda C A, Meyerowitz E M
Division of Biology, California Institute of Technology, Pasadena 91125.
Dev Biol. 1990 May;139(1):121-33. doi: 10.1016/0012-1606(90)90283-o.
The Drosophila glue gene Sgs-3 is specifically expressed in the secretory cells of the salivary glands of third instar larvae. We have assayed the expression of gene fusions to determine the role of cis-acting Sgs-3 sequences in conferring this pattern of expression. These experiments define two regulatory regions required for expression of reporter genes from the Sgs-3 promoter. One region, between 106 and 56 bp upstream of the Sgs-3 mRNA 5' end is sufficient for low but correct tissue- and stage-specific expression. A second region, lying between 629 and 130 bp 5' of the RNA start site is functionally equivalent; that is, it alone will also direct low level, specific expression. These two regions act synergistically to give high level expression. More distant upstream regions function to further increase levels of expression. These two regulatory elements can confer a salivary gland-specific pattern of expression on a heterologous promoter and are also sufficient to drive gene expression in other Drosophila species, implying conservation of regulators.
果蝇黏胶基因Sgs - 3在三龄幼虫唾液腺的分泌细胞中特异性表达。我们检测了基因融合体的表达,以确定顺式作用的Sgs - 3序列在赋予这种表达模式中的作用。这些实验确定了从Sgs - 3启动子表达报告基因所需的两个调控区域。一个区域在Sgs - 3 mRNA 5'端上游106至56 bp之间,足以实现低水平但正确的组织和阶段特异性表达。第二个区域位于RNA起始位点5'端的629至130 bp之间,在功能上是等效的;也就是说,它本身也能指导低水平的特异性表达。这两个区域协同作用以实现高水平表达。更远的上游区域起到进一步提高表达水平的作用。这两个调控元件可以赋予异源启动子唾液腺特异性的表达模式,并且也足以驱动其他果蝇物种中的基因表达,这意味着调控因子具有保守性。