Malachin Giulia, Reiten Malin R, Salvesen Øyvind, Aanes Håvard, Kamstra Jorke H, Skovgaard Kerstin, Heegaard Peter M H, Ersdal Cecilie, Espenes Arild, Tranulis Michael A, Bakkebø Maren K
Faculty of Veterinary Medicine, Norwegian University of Life Sciences, Oslo, Norway.
Department of Microbiology, Division of diagnostics and intervention, Institute of Clinical Medicine, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
PLoS One. 2017 Jun 26;12(6):e0179881. doi: 10.1371/journal.pone.0179881. eCollection 2017.
The cellular prion protein (PrPC) has been extensively studied because of its pivotal role in prion diseases; however, its functions remain incompletely understood. A unique line of goats has been identified that carries a nonsense mutation that abolishes synthesis of PrPC. In these animals, the PrP-encoding mRNA is rapidly degraded. Goats without PrPC are valuable in re-addressing loss-of-function phenotypes observed in Prnp knockout mice. As PrPC has been ascribed various roles in immune cells, we analyzed transcriptomic responses to loss of PrPC in peripheral blood mononuclear cells (PBMCs) from normal goat kids (n = 8, PRNP+/+) and goat kids without PrPC (n = 8, PRNPTer/Ter) by mRNA sequencing. PBMCs normally express moderate levels of PrPC. The vast majority of genes were similarly expressed in the two groups. However, a curated list of 86 differentially expressed genes delineated the two genotypes. About 70% of these were classified as interferon-responsive genes. In goats without PrPC, the majority of type I interferon-responsive genes were in a primed, modestly upregulated state, with fold changes ranging from 1.4 to 3.7. Among these were ISG15, DDX58 (RIG-1), MX1, MX2, OAS1, OAS2 and DRAM1, all of which have important roles in pathogen defense, cell proliferation, apoptosis, immunomodulation and DNA damage response. Our data suggest that PrPC contributes to the fine-tuning of resting state PBMCs expression level of type I interferon-responsive genes. The molecular mechanism by which this is achieved will be an important topic for further research into PrPC physiology.
细胞朊蛋白(PrPC)因其在朊病毒疾病中的关键作用而受到广泛研究;然而,其功能仍未完全明确。已鉴定出一种独特的山羊品系,其携带一种无义突变,该突变可消除PrPC的合成。在这些动物中,编码PrP的mRNA会迅速降解。缺乏PrPC的山羊对于重新研究在Prnp基因敲除小鼠中观察到的功能丧失表型具有重要价值。由于PrPC在免疫细胞中具有多种作用,我们通过mRNA测序分析了正常山羊幼崽(n = 8,PRNP+/+)和缺乏PrPC的山羊幼崽(n = 8,PRNPTer/Ter)外周血单个核细胞(PBMC)中PrPC缺失后的转录组反应。PBMC通常表达中等水平的PrPC。绝大多数基因在两组中表达相似。然而,一份精心挑选的86个差异表达基因列表区分了这两种基因型。其中约70%被归类为干扰素反应基因。在缺乏PrPC的山羊中,大多数I型干扰素反应基因处于预激活、适度上调状态,倍数变化范围为1.4至3.7。其中包括ISG15、DDX58(RIG-1)、MX1、MX2、OAS1、OAS2和DRAM1,所有这些基因在病原体防御、细胞增殖、凋亡、免疫调节和DNA损伤反应中都发挥着重要作用。我们的数据表明,PrPC有助于微调静息状态PBMC中I型干扰素反应基因的表达水平。实现这一过程的分子机制将是进一步研究PrPC生理学的一个重要课题。