Institut Pasteur, Unité Dynamique des Lyssavirus et Adaptation à l'Hôte, Paris, France.
PLoS Pathog. 2012;8(12):e1003060. doi: 10.1371/journal.ppat.1003060. Epub 2012 Dec 13.
NF-κB transcription factors are crucial for many cellular processes. NF-κB is activated by viral infections to induce expression of antiviral cytokines. Here, we identified a novel member of the human NF-κB family, denoted RelAp43, the nucleotide sequence of which contains several exons as well as an intron of the RelA gene. RelAp43 is expressed in all cell lines and tissues tested and exhibits all the properties of a NF-κB protein. Although its sequence does not include a transactivation domain, identifying it as a class I member of the NF-κB family, it is able to potentiate RelA-mediated transactivation and stabilize dimers comprising p50. Furthermore, RelAp43 stimulates the expression of HIAP1, IRF1, and IFN-β - three genes involved in cell immunity against viral infection. It is also targeted by the matrix protein of lyssaviruses, the agents of rabies, resulting in an inhibition of the NF-κB pathway. Taken together, our data provide the description of a novel functional member of the NF-κB family, which plays a key role in the induction of anti-viral innate immune response.
NF-κB 转录因子对于许多细胞过程至关重要。NF-κB 被病毒感染激活,以诱导抗病毒细胞因子的表达。在这里,我们鉴定了人类 NF-κB 家族的一个新成员,称为 RelAp43,其核苷酸序列包含几个外显子以及 RelA 基因的内含子。RelAp43 在所有测试的细胞系和组织中表达,并表现出 NF-κB 蛋白的所有特性。尽管其序列不包含转录激活域,但它被鉴定为 NF-κB 家族的 I 类成员,能够增强 RelA 介导的转录激活并稳定包含 p50 的二聚体。此外,RelAp43 刺激 HIAP1、IRF1 和 IFN-β 的表达 - 这三个基因参与细胞对病毒感染的免疫反应。它也是狂犬病病毒(狂犬病的病原体)基质蛋白的靶标,导致 NF-κB 途径的抑制。总之,我们的数据提供了 NF-κB 家族的一个新的功能成员的描述,该成员在诱导抗病毒先天免疫反应中起关键作用。