Wu Chun-Xiao, Zhao Wen-Pu, Kishi Hiroyuki, Dokan Junichi, Jin Zhe-Xiong, Wei Xing-Cheng, Yokoyama Kazunari K, Muraguchi Atsushi
Department of Immunology, Faculty of Medicine, Toyama Medical and Pharmaceutical University, 2630, Sugitani, Toyama 930-0194, Japan.
Biochem Biophys Res Commun. 2004 May 14;317(4):1096-102. doi: 10.1016/j.bbrc.2004.03.159.
Recombination activating gene-1 (RAG-1) and RAG-2 are expressed specifically in lymphocytes undergoing the antigen receptor gene rearrangement during the lymphocyte development. Our previous study showed that the -41 to -17 nucleotides (nt) 5' -upstream region of mouse RAG-2 were pre-requisite for the core promoter activity and that Pax-5/c-Myb/LEF-1 protein-protein complex was responsible for its activity in immature B cells. In this study, we show that the -65/-42 sequence, the non-conserved sequence between human and mouse RAG-2 promoter, is necessary for the full promoter activity for mouse RAG-2. Electrophoresis mobility shift assay revealed that Myc-associated zinc finger protein (MAZ) as well as SP1/3 binds a GA box in this region. Using chromatin immunoprecipitation, we show that MAZ binds the RAG-2 promoter region in pre-B cells. Furthermore, we show that MAZ synergistically activates the murine RAG-2 promoter with Pax-5/c-Myb/LEF-1 complex. These results first demonstrate that MAZ participates in activation of mouse RAG-2 promoter.
重组激活基因-1(RAG-1)和RAG-2在淋巴细胞发育过程中经历抗原受体基因重排的淋巴细胞中特异性表达。我们之前的研究表明,小鼠RAG-2基因5'上游区域的-41至-17核苷酸(nt)是核心启动子活性的先决条件,并且Pax-5/c-Myb/LEF-1蛋白复合物在未成熟B细胞中负责其活性。在本研究中,我们表明,-65 / -42序列,即人类和小鼠RAG-2启动子之间的非保守序列,对于小鼠RAG-2的完全启动子活性是必需的。电泳迁移率变动分析显示,Myc相关锌指蛋白(MAZ)以及SP1/3结合该区域的一个GA盒。使用染色质免疫沉淀,我们表明MAZ在pre-B细胞中结合RAG-2启动子区域。此外,我们表明MAZ与Pax-5/c-Myb/LEF-1复合物协同激活小鼠RAG-2启动子。这些结果首次证明MAZ参与小鼠RAG-2启动子的激活。