Cadigan K M, Grossniklaus U, Gehring W J
Biozentrum, University of Basel, Switzerland.
Genes Dev. 1994 Apr 15;8(8):899-913. doi: 10.1101/gad.8.8.899.
During germ-band extension in the Drosophila embryo, intercellular communication is required to maintain gene expression patterns initiated at cellular blastoderm. For example, the wingless (wg) single-cell-wide stripe in each parasegment (PS) is dependent on a signal from the adjacent, posterior cells, which express engrailed (eN). This signal is thought to be the hedgehog (hh) gene product, which antagonizes the activity of patched (ptc), a repressor of wg expression. Genetic evidence indicates that the hh signal is bidirectional, but wg transcription is only derepressed on the anterior side of the en/hh stripes. To explain the asymmetric response of the wg promoter to the hh signal, current models predict that each PS is divided into cells that are competent to express either wg or en, but not both. The sloppy paired (slp) locus contains two transcription units, both encoding proteins containing a forkhead domain, a DNA-binding motif. Removal of slp gene function causes embryos to exhibit a severe pair-rule/segment polarity phenotype. We show that the en stripes expand anteriorly in slp mutant embryos and that slp activity is an absolute requirement for maintenance of wg expression at the same time that wg transcription is dependent on hh. The slp proteins are expressed in broad stripes just anterior of the en-positive cells, overlapping the narrow wg stripes. We propose that by virtue of their ability to activate wg and repress en expression, the distribution of the slp proteins define the wg-competent and en-competent groups. Consistent with this hypothesis, ubiquitous expression of slp protein throughout the PS abolishes en expression and, in ptc mutant embryos, results in a near ubiquitous distribution of wg transcripts. In addition to demonstrating the role of slp in maintaining segment polarity, our results suggest that slp works in, or parallel with, the ptc/hh signal transduction pathway to regulate wg transcription.
在果蝇胚胎的胚带延伸过程中,需要细胞间通讯来维持在细胞胚盘阶段启动的基因表达模式。例如,每个副节(PS)中单个细胞宽度的无翅(wg)条纹依赖于来自相邻后细胞的信号,这些后细胞表达 engrailed(en)。该信号被认为是刺猬(hh)基因产物,它拮抗patched(ptc)的活性,ptc是wg表达的抑制因子。遗传证据表明hh信号是双向的,但wg转录仅在en/hh条纹的前侧被解除抑制。为了解释wg启动子对hh信号的不对称反应,目前的模型预测每个PS被分为有能力表达wg或en但不能同时表达两者的细胞。草率配对(slp)基因座包含两个转录单元,两者都编码含有叉头结构域(一种DNA结合基序)的蛋白质。去除slp基因功能会导致胚胎表现出严重的成对规则/节段极性表型。我们发现en条纹在slp突变胚胎中向前扩展,并且slp活性是维持wg表达的绝对必要条件,同时wg转录依赖于hh。slp蛋白在en阳性细胞前方的宽条纹中表达,与狭窄的wg条纹重叠。我们提出,凭借其激活wg和抑制en表达的能力,slp蛋白的分布定义了wg有能力和en有能力的细胞群。与该假设一致,在整个PS中普遍表达slp蛋白会消除en表达,并且在ptc突变胚胎中,会导致wg转录本几乎普遍分布。除了证明slp在维持节段极性中的作用外,我们的结果还表明slp在ptc/hh信号转导途径中起作用或与之平行,以调节wg转录。