Gergen J P, Wieschaus E F
Dev Biol. 1985 Jun;109(2):321-35. doi: 10.1016/0012-1606(85)90459-2.
The runt gene is required in a developing Drosophila embryo for proper segmentation. Mutant embryos fail to hatch but secrete a larval cuticle in which pattern defects are apparent. In runt embryos, there are pattern deletions spaced at two segment intervals along the antero-posterior axis of the animal. The deleted regions are replaced by mirror-image duplications of the remaining regions. This paper investigates the localized requirements for runt+ activity by analyzing the segmentation patterns in larval genetic mosaics. This analysis is aided by the faintoid and shavenbaby mutations which affect larval cuticle morphology without affecting segmentation. These two mutations serve as markers of the regions of larval cuticle secreted by genetically runt cells. The analysis of the runt mosaic patterns indicates the effects of the gene on segmentation are primarily cell autonomous. This includes both the pattern deletions and the associated mirror-image duplications. This indicates the mirror-image duplications are not due to regeneration but result from a more direct effect of runt on patterning in the embryo. The mosaic patterns also reveal other aspects of the process of pattern formation in the larval epidermis. Based on these results a model is presented for the generation of the larval pattern.
在发育中的果蝇胚胎中,矮小基因对于正确的体节形成是必需的。突变胚胎无法孵化,但会分泌出一种幼虫表皮,其中的模式缺陷很明显。在矮小基因胚胎中,沿着动物的前后轴,存在以两个体节间隔排列的模式缺失。缺失区域被其余区域的镜像重复所取代。本文通过分析幼虫遗传嵌合体中的体节模式,研究了矮小基因活性的局部需求。这种分析借助了微弱突变和无毛幼虫突变,这两种突变影响幼虫表皮形态但不影响体节形成。这两种突变作为由遗传上矮小细胞分泌的幼虫表皮区域的标记。对矮小基因嵌合模式的分析表明,该基因对体节形成的影响主要是细胞自主的。这包括模式缺失和相关的镜像重复。这表明镜像重复不是由于再生,而是矮小基因对胚胎模式形成更直接作用的结果。嵌合模式还揭示了幼虫表皮模式形成过程的其他方面。基于这些结果,提出了一个幼虫模式生成的模型。