Sotillos S, Campuzano S
Centro de Biología Molecular Severo Ochoa, CSIC and UAM Cantoblanco, Spain.
Development. 2000 Dec;127(24):5427-38. doi: 10.1242/dev.127.24.5427.
We have identified a novel Drosophila gene, DRacGAP, which behaves as a negative regulator of &Rgr;-family GTPases DRac1 and DCdc42. Reduced function of DRacGAP or increased expression of DRac1 in the wing imaginal disc cause similar effects on vein and sensory organ development and cell proliferation. These effects result from enhanced activity of the EGFR/Ras signalling pathway. We find that in the wing disc, DRac1 enhances EGFR/Ras-dependent activation of MAP Kinase in the prospective veins. Interestingly, DRacGAP expression is negatively regulated by the EGFR/Ras pathway in these regions. During vein formation, local DRacGAP repression would ensure maximal activity of Rac and, in turn, of Ras pathways in vein territories. Additionally, maximal expression of DRacGAP at the vein/intervein boundaries would help to refine the width of the veins. Hence, control of DRacGAP expression by the EGFR/Ras pathway is a previously undescribed feedback mechanism modulating the intensity and/or duration of its signalling during Drosophila development.
我们鉴定出一个新的果蝇基因DRacGAP,它作为Rho家族GTP酶DRac1和DCdc42的负调控因子发挥作用。翅成虫盘内DRacGAP功能的降低或DRac1表达的增加,对翅脉和感觉器官发育以及细胞增殖产生相似的影响。这些影响是由EGFR/Ras信号通路活性增强所致。我们发现,在翅盘中,DRac1增强了预期翅脉中EGFR/Ras依赖的丝裂原活化蛋白激酶(MAP激酶)的激活。有趣的是,在这些区域中,DRacGAP的表达受到EGFR/Ras通路的负调控。在翅脉形成过程中,局部DRacGAP的抑制将确保Rac以及进而Ras通路在翅脉区域的最大活性。此外,DRacGAP在翅脉/翅脉间边界处的最大表达将有助于细化翅脉的宽度。因此,EGFR/Ras通路对DRacGAP表达的调控是一种先前未被描述的反馈机制,在果蝇发育过程中调节其信号传导的强度和/或持续时间。