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Molecular characterisation of ILRUN a novel inhibitor of proinflammatory and antimicrobial cytokines

机译:ILRUN促炎和抗菌细胞因子的新型抑制剂的分子表征

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摘要

Regulation of type-I interferon (IFN) production is essential to the balance between antimicrobial defence and autoimmune disorders. The human protein-coding gene ILRUN (inflammation and lipid regulator with UBA-like and NBR1-like domains, previously C6orf106) was recently characterised as an inhibitor of antiviral and proinflammatory cytokine (interferon-alpha/beta and tumor necrosis factor alpha) transcription. Currently there is a paucity of information about the molecular characteristics of ILRUN, despite it being associated with several diseases including virus infection, coronary artery disease, obesity and cancer. Here, we characterise ILRUN as a highly phylogenetically conserved protein containing UBA-like and a NBR1-like domains that are both essential for inhibition of type-I interferon and tumor necrosis factor alpha) transcription in human cells. We also solved the crystal structure of the NBR1-like domain, providing insights into its potential role in ILRUN function. This study provides critical information for future investigations into the role of ILRUN in health and disease.
机译:调节I型干扰素(IFN)的产生对于抗菌防御和自身免疫性疾病之间的平衡至关重要。人类蛋白编码基因ILRUN(具有UBA样和NBR1样结构域的炎症和脂质调节剂,以前称为C6orf106)最近被表征为抗病毒和促炎细胞因子(干扰素-α/β和肿瘤坏死因子α)转录的抑制剂。尽管ILRUN与几种疾病有关,包括病毒感染,冠状动脉疾病,肥胖和癌症,但目前缺乏有关ILRUN分子特征的信息。在这里,我们将ILRUN表征为高度系统保守的蛋白质,其中包含UBA样和NBR1样域,这两个域对于抑制人细胞中的I型干扰素和肿瘤坏死因子α)转录都是必不可少的。我们还解决了NBR1样域的晶体结构,提供了其在ILRUN功能中潜在作用的见解。该研究为ILRUN在健康和疾病中的作用的未来研究提供了重要信息。

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