Cauvi David M, Cauvi Gabrielle, Pollard K Michael
Department of Molecular and Experimental Medicine, W. M. Keck Autoimmune Disease Center, The Scripps Research Institute, La Jolla, CA 92037, USA.
J Immunol. 2006 Sep 15;177(6):3837-47. doi: 10.4049/jimmunol.177.6.3837.
The complement regulatory protein decay-accelerating factor (DAF or CD55) protects host tissue from complement-mediated injury by inhibiting the classical and alternative complement pathways. Besides its role in complement regulation, DAF has also been shown to be a key player in T cell immunity. Modulation of DAF expression could therefore represent a critical regulatory mechanism in both innate and adaptive immune responses. To identify and characterize key transcriptional regulatory elements controlling mouse Daf1 expression, a 2.5-kb fragment corresponding to the 5' flanking region of the mouse Daf1 gene was cloned. Sequence analysis showed that the mouse Daf1 promoter lacks conventional TATA and CCAAT boxes and displays a high guanine and cytosine content. RACE was used to identify one major and two minor transcription start sites 47, 20, and 17 bp upstream of the translational codon. Positive and negative regulatory regions were identified by transiently transfecting sequential 5'deletion constructs of the 5'flanking region into NIH/3T3, M12.4, and RAW264.7 cells. Mutational analyses of the promoter region combined with Sp1-specific ELISA showed that the transcription factor Sp1 is required for basal transcription and LPS-induced expression of the Daf1 gene. These findings provide new information on the regulation of the mouse Daf1 promoter and will facilitate further studies on the expression of Daf1 during immune responses.
补体调节蛋白衰变加速因子(DAF 或 CD55)通过抑制经典和替代补体途径来保护宿主组织免受补体介导的损伤。除了在补体调节中的作用外,DAF 还被证明是 T 细胞免疫中的关键参与者。因此,DAF 表达的调节可能代表先天性和适应性免疫反应中的一种关键调节机制。为了鉴定和表征控制小鼠 Daf1 表达的关键转录调节元件,克隆了与小鼠 Daf1 基因 5'侧翼区域相对应的 2.5 kb 片段。序列分析表明,小鼠 Daf1 启动子缺乏传统的 TATA 和 CCAAT 框,并且鸟嘌呤和胞嘧啶含量很高。采用 RACE 技术鉴定了翻译密码子上游 47、20 和 17 bp 处的一个主要转录起始位点和两个次要转录起始位点。通过将 5'侧翼区域的连续 5'缺失构建体瞬时转染到 NIH/3T3、M12.4 和 RAW264.7 细胞中,鉴定了正负调节区域。启动子区域的突变分析结合 Sp1 特异性 ELISA 表明,转录因子 Sp1 是 Daf1 基因基础转录和 LPS 诱导表达所必需的。这些发现为小鼠 Daf1 启动子的调节提供了新信息,并将促进对免疫反应期间 Daf1 表达的进一步研究。