Hunninghake G W, Monks B G, Geist L J, Monick M M, Monroy M A, Stinski M F, Webb A C, Dayer J M, Auron P E, Fenton M J
Department of Medicine, University of Iowa College of Medicine, Iowa City 52242.
Mol Cell Biol. 1992 Aug;12(8):3439-48. doi: 10.1128/mcb.12.8.3439-3448.1992.
Prointerleukin 1 beta (IL-1 beta) is a cytokine that mediates a broad range of biological activities. Genomic sequences that regulate IL-1 beta transcription include both inducible regulatory elements located more than 2,700 bp upstream of the transcriptional start site (cap site) and proximal elements located near the TATA box of this gene. In this study, we focused on the identification and characterization of trans-acting nuclear regulatory proteins that bind to the cap site-proximal region of the human IL-1 beta gene. We identified a protein, termed NFIL-1 beta A (NF beta A), that binds to a highly conserved 12-bp DNA sequence (-49 to -38) located upstream of the TATA box motif in both the human and murine IL-1 beta genes. The IL-1 alpha gene, which lacks a TATA motif, does not possess an NF beta A-binding sequence within the promoter region, suggesting that NF beta A may selectively regulate IL-1 beta expression. Using electrophoretic mobility shift assays, we identified several distinct DNA-protein complexes that are expressed in a cell-type-specific manner. In monocytic cell lines, the relative abundance of these complexes varies rapidly following stimulation of the cells with phorbol esters or lipopolysaccharide. UV cross-linking analysis identified two distinct DNA-binding polypeptides that comprise distinct complexes. The functional role of NF beta A was assessed in transient transfection assays. These data indicate that NF beta A is required for both basal and inducible promoter activity in monocytic cells. Furthermore, the human cytomegalovirus immediate-early 1 gene product requires the presence of NF beta A in order to trans-activate the proximal IL-1 beta promoter in a monocytic cell line. We propose that NF beta A is a factor that mediates either direct or indirect activation by the immediate-early 1 gene product. The proximity of this essential factor to the TATA motif suggests a possible role in transcriptional initiation.
前白细胞介素1β(IL-1β)是一种介导多种生物学活性的细胞因子。调节IL-1β转录的基因组序列包括位于转录起始位点(帽位点)上游超过2700 bp的诱导性调控元件和位于该基因TATA盒附近的近端元件。在本研究中,我们专注于鉴定和表征与人IL-1β基因帽位点近端区域结合的反式作用核调节蛋白。我们鉴定出一种名为NFIL-1βA(NFβA)的蛋白,它与人及小鼠IL-1β基因中位于TATA盒基序上游的一个高度保守的12 bp DNA序列(-49至-38)结合。缺乏TATA基序的IL-1α基因在启动子区域内不具有NFβA结合序列,这表明NFβA可能选择性地调节IL-1β的表达。使用电泳迁移率变动分析,我们鉴定出几种以细胞类型特异性方式表达的不同DNA-蛋白质复合物。在单核细胞系中,在用佛波酯或脂多糖刺激细胞后,这些复合物的相对丰度迅速变化。紫外线交联分析鉴定出构成不同复合物的两种不同的DNA结合多肽。通过瞬时转染分析评估了NFβA的功能作用。这些数据表明,NFβA是单核细胞中基础和诱导型启动子活性所必需的。此外人类巨细胞病毒立即早期1基因产物需要NFβA的存在才能在单核细胞系中转激活近端IL-1β启动子。我们提出NFβA是一种介导立即早期1基因产物直接或间接激活的因子。这个必需因子与TATA基序的接近表明其在转录起始中可能发挥作用。