German Cancer Research Center (DKFZ) and University of Heidelberg, Division of Signaling and Functional Genomics, University of Heidelberg, Heidelberg, Germany.
J Innate Immun. 2010;2(2):181-94. doi: 10.1159/000248649. Epub 2009 Oct 13.
Innate immune signalling pathways are evolutionarily conserved between invertebrates and vertebrates. The analysis of NF-kappaB signalling in Drosophila has contributed important insights into how organisms respond to infection. Nevertheless, significant gaps remain in our understanding of how the activation of intracellular signalling elicits specific transcriptional programs. Here we report a genome-wide RNA interference survey for transcription factors that are required for Toll-dependent immune responses. In addition to the NF-kappaB homologs Dif, Dorsal and factors of the general transcription machinery, we identified Deformed Epidermal Autoregulatory Factor 1 (Deaf1) to be required for the expression of the Toll target gene Drosomycin in cultured cells and in Drosophila in vivo. We show that Deaf1 is required for the survival of flies after fungal, but not E. coli, infection. We determine that Deaf1 acts downstream of the NF-kappaB factors Dorsal and Dif. These results indicate that Deaf1 is an important contributor to innate immune responses in vivo.
先天免疫信号通路在无脊椎动物和脊椎动物之间是进化保守的。对果蝇 NF-κB 信号的分析为生物体如何应对感染提供了重要的见解。然而,我们对细胞内信号的激活如何引发特定的转录程序的理解仍然存在很大的差距。在这里,我们报告了一个针对转录因子的全基因组 RNA 干扰筛选,这些转录因子是 Toll 依赖性免疫反应所必需的。除了 NF-κB 同源物 Dif、Dorsal 和一般转录机制的因子外,我们还发现 Deformed Epidermal Autoregulatory Factor 1(Deaf1)对于培养细胞和体内果蝇中 Toll 靶基因 Drosomycin 的表达是必需的。我们表明,Deaf1 是真菌感染后而不是大肠杆菌感染后果蝇存活所必需的。我们确定 Deaf1 作用于 NF-κB 因子 Dorsal 和 Dif 的下游。这些结果表明,Deaf1 是体内先天免疫反应的重要贡献者。