Jaźwińska A, Rushlow C, Roth S
Institut fuer Entwicklungsbiologie, Universitaet zu Koeln, Gyrhofstr. 17, Germany.
Development. 1999 Aug;126(15):3323-34. doi: 10.1242/dev.126.15.3323.
Brinker (Brk), a novel protein with features of a transcriptional repressor, regulates the graded response to Decapentaplegic (Dpp) in appendage primordia of Drosophila. Here, we show that in the embryo brk also has differential effects on Dpp target genes, depending on the level of Dpp activity required for their activation. Low-level target genes, like dpp itself, tolloid and early zerknüllt, show strong ectopic expression in ventrolateral regions of brk mutant embryos; intermediate-level target genes like pannier show weak ectopic expression, while high-level target genes like u-shaped and rhomboid are not affected. Ectopic target gene activation in the absence of brk is independent of Dpp, Tkv and Medea, indicating that Dpp signaling normally antagonizes brk's repression of these target genes. brk is expressed like short gastrulation (sog) in ventrolateral regions of the embryo abutting the dpp domain. Here, both brk and sog antagonize the antineurogenic activity of Dpp so that only in brk sog double mutants is the neuroectoderm completely deleted.
Brinker(Brk)是一种具有转录抑制因子特征的新型蛋白质,它在果蝇附肢原基中调节对Decapentaplegic(Dpp)的梯度反应。在这里,我们表明,在胚胎中,Brk对Dpp靶基因也有不同的影响,这取决于激活它们所需的Dpp活性水平。低水平靶基因,如dpp本身、类 tolloid 蛋白和早期 zerknüllt,在Brk突变胚胎的腹侧区域显示出强烈的异位表达;中等水平靶基因,如 pannier,显示出较弱的异位表达,而高水平靶基因,如 u-shaped 和 rhomboid,则不受影响。在没有Brk的情况下异位激活靶基因独立于Dpp、Tkv和Medea,这表明Dpp信号通常拮抗Brk对这些靶基因的抑制作用。Brk在胚胎腹侧区域与dpp结构域相邻处的表达类似于短原肠胚形成基因(sog)。在这里,Brk和sog都拮抗Dpp的抗神经发生活性,因此只有在Brk和sog双突变体中神经外胚层才会完全缺失。