Flaherty Maria Sol, Zavadil Jiri, Ekas Laura A, Bach Erika A
Pharmacology Department, New York University School of Medicine, New York, New York 10016, USA.
Dev Dyn. 2009 Sep;238(9):2235-53. doi: 10.1002/dvdy.21989.
Although the JAK/STAT pathway regulates numerous processes in vertebrates and invertebrates through modulating transcription, its functionally relevant transcriptional targets remain largely unknown. With one jak and one stat (stat92E), Drosophila provides a powerful system for finding new JAK/STAT target genes. Genome-wide expression profiling on eye discs in which Stat92E is hyperactivated, revealed 584 differentially regulated genes, including known targets domeless, socs36E, and wingless. Other differentially regulated genes (chinmo, lama, Mo25, Imp-L2, Serrate, Delta) were validated and may represent new Stat92E targets. Genetic experiments revealed that Stat92E cell-autonomously represses Serrate, which encodes a Notch ligand. Loss of Stat92E led to de-repression of Serrate in the dorsal eye, resulting in ectopic Notch signaling and aberrant eye growth there. Thus, our micro-array documents a new Stat92E target gene and a previously unidentified inhibitory action of Stat92E on Notch signaling. These data suggest that this study will be a useful resource for the identification of additional Stat92E targets.
尽管JAK/STAT信号通路通过调节转录来调控脊椎动物和无脊椎动物的众多生理过程,但其功能相关的转录靶点仍大多未知。果蝇只有一个jak基因和一个stat基因(stat92E),为寻找新的JAK/STAT靶基因提供了一个强大的系统。对Stat92E过度激活的眼盘进行全基因组表达谱分析,发现了584个差异调节基因,包括已知靶点无穹顶基因(domeless)、细胞因子信号转导抑制因子36E(socs36E)和无翅基因(wingless)。其他差异调节基因(Chinmo、层黏连蛋白α(lama)、Mo25、胰岛素样生长因子结合蛋白Imp-L2、锯齿蛋白(Serrate)、德尔塔蛋白(Delta))得到了验证,可能代表新的Stat92E靶点。遗传学实验表明,Stat92E在细胞自主水平上抑制锯齿蛋白的表达,锯齿蛋白编码一种Notch配体。Stat92E缺失导致背侧眼中锯齿蛋白的去抑制,从而导致异位Notch信号传导和那里的异常眼生长。因此,我们的微阵列记录了一个新的Stat92E靶基因以及Stat92E对Notch信号传导以前未被识别的抑制作用。这些数据表明,这项研究将为鉴定更多的Stat92E靶点提供有用的资源。