Akam M
Department of Genetics, Cambridge, UK.
Development. 1987 Sep;101(1):1-22.
The metameric organization of the Drosophila embryo is generated in the first 5 h after fertilization. An initially rather simple pattern provides the foundation for subsequent development and diversification of the segmented part of the body. Many of the genes that control the formation of this pattern have been identified and at least twenty have been cloned. By combining the techniques of genetics, molecular biology and experimental embryology, it is becoming possible to unravel the role played by each of these genes. The repeating segment pattern is defined by the persistent expression of engrailed and of other genes of the 'segment polarity' class. The establishment of this pattern is directed by a transient molecular prepattern that is generated in the blastoderm by the activity of the 'pair-rule' genes. Maternal determinants at the poles of the egg coordinate this prepattern and define the anteroposterior sequence of pattern elements. The primary effect of these determinants is not known, but genes required for their production have been identified and the product of one of these, bicoid is known to be localized at the anterior of the egg. One early consequence of their activity is to define domains along the A-P axis within which a series of 'cardinal' genes are transcribed. The activity of the cardinal genes is required both to coordinate the process of segmentation and to define the early domains of homeotic gene expression. Further interactions between the homeotic genes and other classes of segmentation genes refine the initial establishment of segment identities.
果蝇胚胎的体节组织在受精后的最初5小时内形成。最初相当简单的模式为身体分节部分的后续发育和多样化奠定了基础。许多控制这种模式形成的基因已被识别,其中至少有二十个已被克隆。通过结合遗传学、分子生物学和实验胚胎学技术,逐渐有可能阐明这些基因各自所起的作用。重复的体节模式由engrailed以及“体节极性”类别的其他基因的持续表达所定义。这种模式的建立由一种短暂的分子预模式引导,该预模式在囊胚层中由“成对规则”基因的活动产生。卵两极的母体决定因素协调这种预模式,并确定模式元件的前后顺序。这些决定因素的主要作用尚不清楚,但已识别出产生它们所需的基因,其中一个基因bicoid的产物已知定位于卵的前部。它们活动的一个早期结果是沿前后轴定义区域,在这些区域内一系列“关键”基因被转录。关键基因的活动对于协调分节过程以及定义同源异型基因表达的早期区域都是必需的。同源异型基因与其他类别的分节基因之间的进一步相互作用完善了体节身份的初始建立。