Mora-López Francisco, Pedreño-Horrillo Nuria, Delgado-Pérez Luis, Brieva José A, Campos-Caro Antonio
Unidad de Investigación, Hospital Universitario Puerta del Mar, Cádiz, Spain.
Eur J Immunol. 2008 Aug;38(8):2316-24. doi: 10.1002/eji.200737861.
The positive regulatory domain containing 1, encoded by the PRDM1 gene, is a transcriptional repressor considered as a master regulator that is required and sufficient for plasma cell differentiation. In the present study we have performed sequence analysis of the upstream region of the human PRDM1 gene to detect the minimal promoter region necessary for PRDM1 gene transcription. This region comprises the region upstream of the initiation site, as well as the first exon. Collectively, deletion and mutation analysis in conjunction with luciferase reporter assays, EMSA and supershift assays identified a phylogenetically conserved GC-box as an essential element for PRDM1 expression. This GC-box element matches to a binding site for multiple transcription factors such as SP1 and SP3 isoforms as well as early growth response 1. Chromatin immunoprecipitation assays confirmed the in vivo binding capability of these factors to the human PRDM1 promoter. These studies together characterize for the first time the basal activity of the human PRDM1 promoter, through which several factors, including SP1, SP3 and early growth response 1, modulate its expression through a conserved GC-box.
由PRDM1基因编码的含1的阳性调节域是一种转录抑制因子,被认为是浆细胞分化所必需且足够的主要调节因子。在本研究中,我们对人类PRDM1基因上游区域进行了序列分析,以检测PRDM1基因转录所需的最小启动子区域。该区域包括起始位点上游区域以及第一个外显子。通过缺失和突变分析并结合荧光素酶报告基因检测、电泳迁移率变动分析(EMSA)和超迁移分析,共同确定了一个系统发育保守的GC盒是PRDM1表达的必需元件。该GC盒元件与多个转录因子的结合位点匹配,如SP1和SP3亚型以及早期生长反应因子1。染色质免疫沉淀分析证实了这些因子在体内与人PRDM1启动子的结合能力。这些研究首次共同表征了人类PRDM1启动子的基础活性,通过该活性,包括SP1、SP3和早期生长反应因子1在内的多种因子通过保守的GC盒调节其表达。