Bienz M, Tremml G
Zoological Institute, University of Zürich, Switzerland.
Nature. 1988 Jun 9;333(6173):576-8. doi: 10.1038/333576a0.
Domains of differential homeotic gene activity are formed at specific positions along the anteroposterior axis of the early Drosophila embryo. Homeotic genes are required continuously throughout development, so that homeotic gene activity has to be maintained independently of the positional information provided in the early embryo. In the ectoderm, the domains of homeotic gene activity partially overlap, but we have found that in the visceral mesoderm at least three of these genes are expressed in adjacent and mutually exclusive domains. It has been proposed that stable, sharply demarcated domains of this type could be established if a homeotic gene product stimulated its own expression locally and inhibited the expression of other homeotic genes, which Meinhardt has termed autocatalysis and mutual exclusion respectively. Furthermore, autocatalysis of this kind can in principle account for the maintenance of homeotic gene activity throughout development. We find that the unique domain of Ultrabithorax (Ubx) expression in the visceral mesoderm is dependent both on autocatalysis and on an exclusion mechanism: Ubx product is required for its own synthesis, whereas the product of the posteriorly adjacent gene abdominal-A represses Ubx expression.
差异同源异型基因活性结构域沿着早期果蝇胚胎的前后轴在特定位置形成。同源异型基因在整个发育过程中持续发挥作用,因此同源异型基因的活性必须独立于早期胚胎中提供的位置信息来维持。在外胚层中,同源异型基因活性结构域部分重叠,但我们发现在内脏中胚层中,这些基因中至少有三个在相邻且相互排斥的结构域中表达。有人提出,如果一个同源异型基因产物在局部刺激自身表达并抑制其他同源异型基因的表达,就可以建立这种稳定、界限分明的结构域,迈因哈特分别将其称为自催化和相互排斥。此外,这种自催化原则上可以解释同源异型基因活性在整个发育过程中的维持。我们发现,内脏中胚层中超双胸(Ubx)表达的独特结构域既依赖于自催化,也依赖于一种排斥机制:Ubx产物是其自身合成所必需的,而后方相邻基因腹部A的产物则抑制Ubx的表达。