Chen Li-Ying, Wang Juinn-Chin, Hyvert Yann, Lin Hui-Ping, Perrimon Norbert, Imler Jean-Luc, Hsu Jui-Chou
Department of Life Science, Institute of Molecular Medicine, National Tsing Hua University, Hsinchu, Taiwan 30034, Republic of China.
Curr Biol. 2006 Jun 20;16(12):1183-93. doi: 10.1016/j.cub.2006.05.050.
The Drosophila Toll pathway takes part in both establishment of the embryonic dorsoventral axis and induction of the innate immune response in adults. Upon activation by the cytokine Spätzle, Toll interacts with the adaptor proteins DmMyD88 and Tube and the kinase Pelle and triggers degradation of the inhibitor Cactus, thus allowing the nuclear translocation of the transcription factor Dorsal/Dif. weckle (wek) was previously identified as a new dorsal group gene that encodes a putative zinc finger transcription factor. However, its role in the Toll pathway was unknown.
Here, we isolated new wek alleles and demonstrated that cactus is epistatic to wek, which in turn is epistatic to Toll. Consistent with this, Wek localizes to the plasma membrane of embryos, independently of Toll signaling. Wek homodimerizes and associates with Toll. Moreover, Wek binds to and localizes DmMyD88 to the plasma membrane. Thus, Wek acts as an adaptor to assemble/stabilize a Toll/Wek/DmMyD88/Tube complex. Remarkably, unlike the DmMyD88/tube/pelle/cactus gene cassette of the Toll pathway, wek plays a minimal role, if any, in the immune defense against Gram-positive bacteria and fungi.
We conclude that Wek is an adaptor to link Toll and DmMyD88 and is required for efficient recruitment of DmMyD88 to Toll. Unexpectedly, wek is dispensable for innate immune response, thus revealing differences in the Toll-mediated activation of Dorsal in the embryo and Dif in the fat body of adult flies.
果蝇Toll信号通路参与胚胎背腹轴的建立以及成虫先天免疫反应的诱导。在细胞因子Spätzle激活后,Toll与接头蛋白DmMyD88和Tube以及激酶Pelle相互作用,并触发抑制剂Cactus的降解,从而使转录因子Dorsal/Dif发生核转位。weckle(wek)先前被鉴定为一个新的背侧组基因,编码一种假定的锌指转录因子。然而,其在Toll信号通路中的作用尚不清楚。
在此,我们分离出了新的wek等位基因,并证明cactus对wek呈上位性,而wek对Toll呈上位性。与此一致的是,Wek定位于胚胎的质膜,与Toll信号无关。Wek形成同源二聚体并与Toll结合。此外,Wek将DmMyD88结合并定位到质膜上。因此,Wek作为一种接头蛋白来组装/稳定Toll/Wek/DmMyD88/Tube复合物。值得注意的是,与Toll信号通路的DmMyD88/tube/pelle/cactus基因盒不同,wek在针对革兰氏阳性细菌和真菌的免疫防御中作用极小(如果有作用的话)。
我们得出结论,Wek是连接Toll和DmMyD88的接头蛋白,是将DmMyD88有效招募到Toll所必需的。出乎意料的是,wek对于先天免疫反应是可有可无的,从而揭示了Toll介导的胚胎中Dorsal激活与成年果蝇脂肪体中Dif激活的差异。