a Department of Molecular, Cell, and Systems Biology , Institute for Integrative Genome Biology, University of California , Riverside , CA , USA.
RNA Biol. 2019 May;16(5):686-695. doi: 10.1080/15476286.2019.1582954. Epub 2019 Mar 4.
RNA binding proteins regulate gene expression through several post-transcriptional mechanisms. The broadly expressed HuR/ELAVL1 is important for proper function of multiple immune cell types, and has been proposed to regulate cytokine and other mRNA 3' UTRs upon activation. However, this mechanism has not been previously dissected in stable cellular settings. In this study, HuR demonstrated strong anti-apoptotic and activation roles in Jurkat T cells. Detailed transcriptomic analysis of HuR knockout cells revealed a substantial negative impact on the activation program, coordinately preventing the expression of immune response gene categories, including all cytokines. Knockout cells showed a significant defect in IL-2 production, which was rescued upon reintroduction of HuR. Interestingly, the mechanism of HuR regulation did not involve control of the cytokine 3' UTRs: HuR knockout did not affect the activity of 3' UTR reporters in 293 cells, and had no effect on IL-2 and TNF 3' UTRs in resting or activated Jurkats. Instead, impaired cytokine production corresponded with defective induction of the IL-2 promoter upon activation. Accordingly, upregulation of NFATC1 was also impaired, without 3' UTR effects. Together, these results indicate that HuR controls cytokine production through coordinated upstream pathways, and that additional mechanisms must be considered in investigating its function.
RNA 结合蛋白通过几种转录后机制调节基因表达。广泛表达的 HuR/ELAVL1 对多种免疫细胞类型的正常功能很重要,并且据推测在激活时可以调节细胞因子和其他 mRNA 3'UTR。然而,这种机制在稳定的细胞环境中尚未被之前的研究解析过。在这项研究中,HuR 在 Jurkat T 细胞中表现出强烈的抗凋亡和激活作用。HuR 敲除细胞的详细转录组分析显示,其对激活程序有实质性的负面影响,协调地阻止了免疫反应基因类别的表达,包括所有细胞因子。敲除细胞在产生 IL-2 方面表现出明显的缺陷,而在重新引入 HuR 后得到了挽救。有趣的是,HuR 调节的机制不涉及细胞因子 3'UTR 的控制:HuR 敲除不会影响 293 细胞中 3'UTR 报告基因的活性,并且在静止或激活的 Jurkat 中对 IL-2 和 TNF 3'UTR 没有影响。相反,细胞因子产生的缺陷与激活时 IL-2 启动子的诱导缺陷相对应。因此,NFATC1 的上调也受到了损害,而没有 3'UTR 的影响。综上所述,这些结果表明 HuR 通过协调的上游途径控制细胞因子的产生,并且在研究其功能时必须考虑其他机制。