Kraut R, Levine M
Department of Biological Sciences, Fairchild Center, Columbia University, New York, NY 10027.
Development. 1991 Feb;111(2):601-9. doi: 10.1242/dev.111.2.601.
We describe the regulated expression of the segmentation gene giant (gt) during early embryogenesis. The gt protein is expressed in two broad gradients in precellular embryos, one in anterior regions and the other in posterior regions. Double immunolocalization studies show that the gt patterns overlap with protein gradients specified by the gap genes hunchback (hb) and knirps (kni). Analysis of all known gap mutants, as well as mutations that disrupt each of the maternal organizing centers, indicate that maternal factors are responsible for initiating gt expression, while gap genes participate in the subsequent refinement of the pattern. The maternal morphogen bicoid (bcd) initiates the anterior gt pattern, while nanos (nos) plays a role in the posterior pattern. Gene dosage studies indicate that different thresholds of the bcd gradient might trigger hb and gt expression, resulting in overlapping but noncoincident patterns of expression. We also present evidence that different concentrations of hb protein are instructive in defining the limits of kni and gt expression within the presumptive abdomen. These results suggest that gt is a bona fide gap gene, which acts with hb, Krüppel and kni to initiate striped patterns of gene expression in the early embryo.
我们描述了分节基因巨头(gt)在胚胎早期发育过程中的调控表达。gt蛋白在前细胞胚胎中以两种广泛的梯度表达,一种在前部区域,另一种在后部区域。双重免疫定位研究表明,gt模式与间隙基因驼背(hb)和克尼普斯(kni)所确定的蛋白质梯度重叠。对所有已知间隙突变体以及破坏每个母体组织中心的突变的分析表明,母体因子负责启动gt表达,而间隙基因参与随后模式的细化。母体形态发生素双尾(bcd)启动前部gt模式,而纳米(nos)在后部模式中起作用。基因剂量研究表明,bcd梯度的不同阈值可能触发hb和gt表达,导致表达模式重叠但不重合。我们还提供证据表明,不同浓度的hb蛋白在确定假定腹部内kni和gt表达的界限方面具有指导作用。这些结果表明,gt是一个真正的间隙基因,它与hb、克鲁佩尔和kni共同作用,在早期胚胎中启动基因表达的条纹模式。