Chen C K, Kühnlein R P, Eulenberg K G, Vincent S, Affolter M, Schuh R
Max-Planck-Institut für biophysikalische Chemie, Abt. Molekulare Entwicklungsbiologie, Am Fassberg, D-37077 Göttingen, Germany.
Development. 1998 Dec;125(24):4959-68. doi: 10.1242/dev.125.24.4959.
Cell migration during embryonic tracheal system development in Drosophila requires DPP and EGF signaling to generate the archetypal branching pattern. We show that two genes encoding the transcription factors KNIRPS and KNIRPS RELATED possess multiple and redundant functions during tracheal development. knirps/knirps related activity is necessary to mediate DPP signaling which is required for tracheal cell migration and formation of the dorsal and ventral branches. Ectopic knirps or knirps related expression in lateral tracheal cells respecifies their anteroposterior to a dorsoventral migration behavior, similar to that observed in the case of ectopic DPP expression. In dorsal tracheal cells knirps/knirps related activity represses the transcription factor SPALT; this repression is essential for secondary and terminal branch formation. However, in cells of the dorsal trunk, spalt expression is required for normal anteroposterior cell migration and morphogenesis. spalt expression is maintained by the EGF receptor pathway and, hence, some of the opposing activities of the EGF and DPP signaling pathways are mediated by spalt and knirps/knirps related. Furthermore, we provide evidence that the border between cells acquiring dorsal branch and dorsal trunk identity is established by the direct interaction of KNIRPS with a spalt cis-regulatory element.
在果蝇胚胎气管系统发育过程中,细胞迁移需要DPP和EGF信号传导来生成典型的分支模式。我们发现,编码转录因子KNIRPS和KNIRPS RELATED的两个基因在气管发育过程中具有多种冗余功能。knirps/knirps related活性对于介导DPP信号传导是必需的,而DPP信号传导是气管细胞迁移以及背侧和腹侧分支形成所必需的。在外侧气管细胞中异位表达knirps或knirps related会将它们的前后迁移行为重新指定为背腹迁移行为,这与异位表达DPP时观察到的情况相似。在背侧气管细胞中,knirps/knirps related活性会抑制转录因子SPALT;这种抑制对于二级和终末分支的形成至关重要。然而,在背干细胞中,spalt表达对于正常的前后细胞迁移和形态发生是必需的。spalt表达由EGF受体途径维持,因此,EGF和DPP信号传导途径的一些相反活性是由spalt和knirps/knirps related介导的。此外,我们提供的证据表明,获得背侧分支和背干身份的细胞之间的边界是由KNIRPS与spalt顺式调控元件的直接相互作用建立的。