Omori S A, Smale S, O'Shea-Greenfield A, Wall R
Molecular Biology Institute and Department of Microbiology and Immunology, University of California School of Medicine, Los Angeles 90095, USA.
J Immunol. 1997 Aug 15;159(4):1800-8.
The leukocyte-specific, cytoskeleton-binding pp52 (LSP-1, WP-34) protein is widely expressed in multiple leukocyte lineages, including B and T lymphocytes, granulocytes, and macrophages. We previously detected a tissue-specific promoter preceding the exon encoding the N terminus of the pp52 leukocyte protein. Here we describe the functional characterization of this promoter and identification of the factors in B and T cells that regulate its activity. The pp52 promoter contains an initiator specifying the unique 5' terminus of pp52 mRNA, tandem pairs of Ets and SP1 motifs, and a lone C/EBP motif. All these motifs are essential and collectively control transcriptional activity. DNA binding studies and Ab supershift assays revealed that different combinations of factors interact with these motifs in B cells vs T cells. The Ets motifs are preferentially bound by PU-1 in B cell extracts from all stages of development, whereas a different Ets family member reacts with these motifs in T cell extracts. The C/EBP motif is bound by Ig/EBP-1 in pre-B cell and T cell extracts, but is replaced by nuclear factor-IL-6beta or a nuclear factor-IL-6beta-Ig/EBP-1 heterodimer in plasmacytoma cell extracts. Despite its reported role as a negative regulator of transcription, Ig/EBP-1 appears to exert a stimulatory effect on this promoter. These findings reveal the features controlling the pp52 promoter in B and T cells and provide the foundation for determining the regulation of this promoter in other leukocyte lineages.
白细胞特异性细胞骨架结合蛋白pp52(LSP-1,WP-34)在多种白细胞谱系中广泛表达,包括B淋巴细胞、T淋巴细胞、粒细胞和巨噬细胞。我们之前在编码pp52白细胞蛋白N端的外显子之前检测到一个组织特异性启动子。在此,我们描述了该启动子的功能特性,并鉴定了B细胞和T细胞中调节其活性的因子。pp52启动子包含一个决定pp52 mRNA独特5'末端的起始子、Ets和SP1基序的串联对以及一个单独的C/EBP基序。所有这些基序都是必需的,并共同控制转录活性。DNA结合研究和抗体超迁移分析表明,B细胞和T细胞中不同的因子组合与这些基序相互作用。在发育各阶段的B细胞提取物中,Ets基序优先与PU-1结合,而在T细胞提取物中,另一个Ets家族成员与这些基序反应。在pre-B细胞和T细胞提取物中,C/EBP基序与Ig/EBP-1结合,但在浆细胞瘤细胞提取物中被核因子-IL-6β或核因子-IL-6β-Ig/EBP-1异二聚体取代。尽管据报道Ig/EBP-1作为转录负调节因子发挥作用,但它似乎对该启动子发挥刺激作用。这些发现揭示了B细胞和T细胞中控制pp52启动子的特征,并为确定该启动子在其他白细胞谱系中的调控奠定了基础。