Carroll S B, Winslow G M, Schüpbach T, Scott M P
Nature. 1986;323(6085):278-80. doi: 10.1038/323278a0.
Several genes have been identified that are involved in establishing the segmented body pattern during development of the fruit-fly Drosophila melanogaster. These fall into several classes on the basis of the kind of alteration to the wild-type segmentation pattern observed in mutant embryos. For example, mutations of the pair-rule class, such as fushi tarazu (ftz), cause the deletion of pattern elements with a two-segment periodicity; those of the gap class, such as knirps, cause the deletion of contiguous groups of segments. The availability of antibodies against the ftz protein has allowed its spatial pattern of expression to be studied during the development of wild-type and mutant embryos. The aim of the latter kind of experiment is to investigate possible interactions between these important genes. We have recently reported that knirps mutations cause a striking alteration to the pattern of transverse stripes of ftz expression usually seen during embryogenesis. Knirps is a zygotically-expressed gene, but recently a class of maternally-active genes has been identified that causes similar defects in pattern formation. We have now investigated the pattern of ftz expression in mutants of this class and have found that while they do have features seen in knirps mutants, they also exhibit significant differences between the different mutations reflecting the distinct but overlapping domains of gene activity. These observations demonstrate that maternally-active segmentation genes regulate zygotic gene expression, and that some of their effects on ftz may be directed through the knirps gene.
在果蝇黑腹果蝇的发育过程中,已经鉴定出几个参与建立分节身体模式的基因。根据在突变胚胎中观察到的对野生型分节模式的改变类型,这些基因可分为几类。例如,成对规则类的突变,如ftz(腹节基因),会导致具有两体节周期性的模式元素缺失;间隙类的突变,如克尼普斯基因,会导致相邻节段组的缺失。针对ftz蛋白的抗体的可用性使得能够在野生型和突变胚胎的发育过程中研究其空间表达模式。后一种实验的目的是研究这些重要基因之间可能的相互作用。我们最近报道,克尼普斯突变会导致胚胎发生过程中通常出现的ftz表达横向条纹模式发生显著改变。克尼普斯是一个合子表达基因,但最近已经鉴定出一类母体活性基因,它们在模式形成中会导致类似的缺陷。我们现在研究了这一类突变体中ftz的表达模式,发现虽然它们确实具有克尼普斯突变体中所见的特征,但不同突变之间也存在显著差异,这反映了基因活性的不同但重叠的结构域。这些观察结果表明,母体活性分节基因调节合子基因表达,并且它们对ftz的一些影响可能是通过克尼普斯基因介导的。