Immunoregulation, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Faculty of Information Technology and Bionics, Pázmány Péter Catholic University, Budapest, Hungary.
Front Immunol. 2021 Feb 18;12:630389. doi: 10.3389/fimmu.2021.630389. eCollection 2021.
The proprotein convertase enzyme FURIN promotes the proteolytic maturation of pro-proteins and thereby it serves as an important factor for maintaining cellular homeostasis. In T cells, FURIN is critical for maintaining the T regulatory cell dependent peripheral immune tolerance and intact T helper cell polarization. The enzymatic activity of FURIN is directly associated with its expression levels, but genetic determinants for cell-type specific gene regulation have remained elusive. By exploring the histone acetyltransferase p300 binding patterns in T helper cells, a putative regulatory region at ca. 20kB upstream of gene was identified. When this region was deleted with CRISPR/Cas9 the production of mRNA was significantly reduced in activated mouse T cells. Genome-wide RNA profiling by sequencing revealed that the novel regulator region also impacted the expression of several genes that have previously been associated with the Th1 type hall mark cytokine IFNγ regulation or function. Finally, genetic regulatory region was found to specifically promote the secretion of IFNγ by activated T cells. In sum, our data unravels the presence of expression regulatory region in T cells that has characteristics of a super-enhancer for Th1 cell fate.
蛋白水解酶 FURIN 促进前体蛋白的蛋白水解成熟,因此它是维持细胞内稳态的重要因素。在 T 细胞中,FURIN 对于维持 T 调节细胞依赖的外周免疫耐受和完整的 T 辅助细胞极化至关重要。FURIN 的酶活性与其表达水平直接相关,但细胞类型特异性基因调控的遗传决定因素仍然难以捉摸。通过探索 T 辅助细胞中的组蛋白乙酰转移酶 p300 的结合模式,在 基因的上游约 20kb 处鉴定出一个假定的调控区。当使用 CRISPR/Cas9 对该区域进行缺失时,激活的小鼠 T 细胞中 的 mRNA 产生明显减少。通过测序进行的全基因组 RNA 谱分析表明,该新的 调控区还影响了先前与 Th1 型标志性细胞因子 IFNγ 调节或功能相关的几个基因的表达。最后,发现 基因调控区可特异性促进激活的 T 细胞分泌 IFNγ。总之,我们的数据揭示了 T 细胞中存在 的表达调控区,该调控区具有 Th1 细胞命运的超级增强子特征。