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Identification of DEAD-Box RNA Helicase DDX41 as a Trafficking Protein That Involves in Multiple Innate Immune Signaling Pathways in a Zebrafish Model

机译:DEAD-Box RNA解旋酶DDX41作为涉及斑马鱼模型中多个先天免疫信号通路的贩运蛋白的鉴定

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摘要

DDX41 is an important sensor for host recognition of DNA viruses and initiation of nuclear factor-κB (NF-κB) and IFN signaling pathways in mammals. However, its occurrence and functions in other vertebrates remain poorly defined. Here, a DDX41 ortholog [Danio rerio DDX41 (DrDDX41)] with various conserved structural features to its mammalian counterparts was identified from a zebrafish model. This DrDDX41 was found to be a trafficking protein distributed in the nucleus of resting cells but transported into the cytoplasm under DNA stimulation. Two nuclear localization signal motifs were localized beside the coiled-coil domain, whereas one nuclear export signal motif existed in the DEADc domain. DrDDX41 acts as an initiator for the activation of NF-κB and IFN signaling pathways in a Danio rerio STING (DrSTING)-dependent manner through its DEADc domain, which is a typical performance of mammalian DDX41. These observations suggested the conservation of DDX41 proteins throughout the vertebrate evolution, making zebrafish an alternative model in understanding DDX41-mediated immunology. With this model system, we found that DrDDX41 contributes to DrSTING–Danio rerio STAT6 (DrSTAT6)-mediated chemokine (Danio rerio CCL20) production through its DEADc domain. To the best of our knowledge, this work is the first report showing that DDX41 is an upstream initiator in this newly identified signaling pathway. The DrDDX41-mediated signaling pathways play important roles in innate antibacterial immunity because knockdown of either DrDDX41 or DrSTING/DrSTAT6 significantly reduced the survival of zebrafish under Aeromonas hydrophilia or Edwardsiella tarda infection. Our findings would enrich the current knowledge of DDX41-mediated immunology and the evolutionary history of the DDX41 family.
机译:DDX41是一种重要的传感器,可用于宿主识别DNA病毒以及哺乳动物中核因子-κB(NF-κB)和IFN信号通路的启动。但是,它在其他脊椎动物中的发生和功能仍然不清楚。在这里,从斑马鱼模型中鉴定了具有与哺乳动物对应物不同的保守结构特征的DDX41直系同源物[Danio rerio DDX41(DrDDX41)]。发现该DrDDX41是一种运输蛋白,分布在静止细胞的细胞核中,但在DNA刺激下被运输到细胞质中。在线圈螺旋结构域旁边定位了两个核定位信号基序,而在DEADc结构域中存在一个核输出信号基序。 DrDDX41通过其DEADc结构域以依赖Danio rerio STING(DrSTING)的方式作为激活NF-κB和IFN信号通路的引发剂,这是哺乳动物DDX41的典型表现。这些观察结果表明,DDX41蛋白在整个脊椎动物进化过程中都得到了保护,使得斑马鱼成为了理解DDX41介导的免疫学的替代模型。通过此模型系统,我们发现DrDDX41通过其DEADc结构域有助于DrSTING–Danio rerio STAT6(DrSTAT6)介导的趋化因子(Danio rerio CCL20)的生产。据我们所知,这项工作是第一个报告,表明DDX41是这一新发现的信号通路的上游启动子。 DrDDX41介导的信号通路在先天的抗菌免疫中起着重要的作用,因为击倒DrDDX41或DrSTING / DrSTAT6会大大降低斑马鱼在嗜水气单胞菌或感染下的存活率。我们的发现将丰富DDX41介导的免疫学的最新知识以及DDX41家族的进化史。

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