Dunne Jonathan C, Kondylis Vangelis, Rabouille Catherine
The Wellcome Trust Centre for Cell Biology, ICMB, The Michael Swann Building, University of Edinburgh, Mayfield Road, Edinburgh EH9 3JR, Scotland, UK.
Dev Biol. 2002 May 1;245(1):172-86. doi: 10.1006/dbio.2002.0632.
One of the most significant morphogenic events in the development of Drosophila melanogaster is the elongation of imaginal discs during puparium formation. We have shown that this macroscopic event is accompanied by the formation of Golgi stacks from small Golgi larval clusters of vesicles and tubules that are present prior to the onset of disc elongation. We have shown that the fly steroid hormone 20-hydroxyecdysone triggers both the elongation itself and the formation of Golgi stacks (V. Kondylis, S. E. Goulding, J. C. Dunne, and C. Rabouille, 2001, Mol. Biol. Cell, 12, 2308). Using mRNA in situ hybridisation, we show here that ecdysone triggers the upregulation of a subset of genes encoding Golgi-related proteins (such as dnsf1, dsec23, dsed5, and drab1) and downregulates the expression of others (such as dergic53, dbeta'COP, and drab6). We show that the transcription factor Broad-complex, itself an "early" ecdysone target, mediates this regulation. And we show that the ecdysone-independent upregulation of dnsf1 and dsnap prior to the ecdysone peak leads to a precocious formation of large Golgi stacks. The ecdysone-triggered biogenesis of Golgi stacks at the onset of imaginal disc elongation offers the exciting possibility of advancing our understanding of the relationship between gene expression and organelle biogenesis.
黑腹果蝇发育过程中最重要的形态发生事件之一是化蛹期成虫盘的伸长。我们已经表明,这一宏观事件伴随着高尔基体堆叠的形成,这些高尔基体堆叠由盘伸长开始前就存在的小的高尔基体幼虫囊泡和小管簇形成。我们已经表明,果蝇类固醇激素20-羟基蜕皮激素触发了伸长本身以及高尔基体堆叠的形成(V. 康迪利斯、S. E. 古尔丁、J. C. 邓恩和C. 拉布耶,2001年,《分子生物学细胞》,12卷,2308页)。利用mRNA原位杂交技术,我们在此表明蜕皮激素触发了一组编码高尔基体相关蛋白(如dnsf1、dsec23、dsed5和drab1)的基因的上调,并下调了其他一些基因(如dergic53、dbeta'COP和drab6)的表达。我们表明转录因子Broad-complex本身是一个“早期”蜕皮激素靶点,介导了这种调控。并且我们表明在蜕皮激素峰值之前dnsf1和dsnap的不依赖蜕皮激素的上调导致了大型高尔基体堆叠的早熟形成。在成虫盘伸长开始时蜕皮激素触发的高尔基体堆叠的生物发生为推进我们对基因表达与细胞器生物发生之间关系的理解提供了令人兴奋的可能性。