Gorman M J, Kaufman T C
Howard Hughes Medical Institute, Department of Biology, Indiana University, Bloomington 47405, USA.
Genetics. 1995 Jun;140(2):557-72. doi: 10.1093/genetics/140.2.557.
The homeotic gene Sex combs reduced (Scr) of Drosophila melanogaster is expressed in the labial and prothoracic segments of the ectoderm, in parasegments two and three of the CNS, and in the visceral mesoderm of the anterior and posterior midgut. The mutationally defined function of Scr is to specify the identity of the labial and prothoracic segments and to control the development of the gastric caeca. The Scr locus occupies a chromosomal region of approximately 80 kb within the Antennapedia complex (ANT-C). To understand how Scr's spatiotemporal expression pattern is generated in the embryo, we have mapped its transcriptional regulatory elements using three approaches. First, we examined the expression pattern of Scr in embryos containing chromosomal rearrangements that remove potential Scr regulatory elements. Second, we made and analyzed a set of Scr minigene transformants. Third, we analyzed a set of Scr-lacZ enhancer tester constructs. Using more sensitive anti-SCR antisera, we discovered that Scr is expressed in tissues that were not previously thought to accumulate SCR: a stripe of ectodermal cells in the parasegment 2 region of stage 5 embryos, the embryonic salivary glands, and the dorsal ridge. Four DNA fragments that had previously been shown in an analysis of Scr-lacZ reporter constructs to contain putative Scr enhancer elements were found to have functional enhancers; similarly, another Scr fragment was found to contain a functional repressor. Our results suggest that regulation of Scr in the labial segment and the CNS requires the apparently synergistic action of multiple, widely spaced enhancer elements. Regulation in the prothorax also appears to be controlled by multiple enhancers:one complete pattern element and one subpattern element. In contrast, Scr regulation in the visceral mesoderm is controlled by an enhancer(s) located in only one DNA fragment.
果蝇黑腹果蝇的同源异型基因性梳减少(Scr)在外胚层的唇节和前胸节、中枢神经系统的副节2和3以及前后中肠的内脏中胚层中表达。Scr经突变定义的功能是确定唇节和前胸节的身份,并控制胃盲囊的发育。Scr基因座位于触角足复合体(ANT-C)内约80 kb的染色体区域。为了了解Scr在胚胎中的时空表达模式是如何产生的,我们使用了三种方法来绘制其转录调控元件。首先,我们检查了含有消除潜在Scr调控元件的染色体重排的胚胎中Scr的表达模式。其次,我们构建并分析了一组Scr微基因转化体。第三,我们分析了一组Scr-lacZ增强子测试构建体。使用更敏感的抗SCR抗血清,我们发现Scr在以前认为不会积累SCR的组织中表达:5期胚胎副节2区域的一条外胚层细胞带、胚胎唾液腺和背脊。在对Scr-lacZ报告构建体的分析中,先前显示包含推定Scr增强子元件的四个DNA片段被发现具有功能性增强子;同样,另一个Scr片段被发现包含一个功能性阻遏物。我们的结果表明,唇节和中枢神经系统中Scr的调控需要多个广泛间隔的增强子元件的明显协同作用。前胸的调控似乎也由多个增强子控制:一个完整模式元件和一个子模式元件。相比之下,内脏中胚层中Scr的调控由仅位于一个DNA片段中的一个增强子控制。