Arman Mònica, Aguilera-Montilla Noemí, Mas Virgínia, Puig-Kröger Amaya, Pignatelli Miguel, Guigó Roderic, Corbí Angel-Luis, Lozano Francisco
Servei d'Immunologia, Hospital Clínic Universitari de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Facultat de Medicina, Universitat de Barcelona, Villarroel 170, 08036 Barcelona, Spain.
Mol Immunol. 2009 Jul;46(11-12):2226-35. doi: 10.1016/j.molimm.2009.04.018. Epub 2009 May 14.
CD6 is a lymphocyte surface receptor involved in lymphocyte activation and differentiation processes that is constitutively expressed on developing and mature T cells and on the B1a cells. To define the molecular basis for the tissue-specific expression of CD6 we have identified the transcription factors that control the activity of the proximal regulatory region of the human CD6 gene. The TATA-less CD6 promoter contains multiple transcriptional start sites, and its preferential activity in human T lymphocytes is dependent on RUNX- and Ets-binding sites located within a highly conserved region. RUNX and Ets-1 factors transactivated the CD6 promoter through recognition of the -215 and -230 binding sites, respectively. Chromatin immunoprecipitation assays revealed that RUNX1 constitutively occupies the CD6 promoter in vivo, and knockdown experiments demonstrated that the steady-state level of CD6 mRNA is dependent on the expression of RUNX1, RUNX3 and Ets-1 transcription factors. Therefore, RUNX1/3 and Ets1 control the expression of CD6 in human T lymphocytes, thus expanding the range of T-cell specific and developmentally regulated lymphocyte gene targets involved in T-cell activation and differentiation.
CD6是一种参与淋巴细胞激活和分化过程的淋巴细胞表面受体,在发育中的和成熟的T细胞以及B1a细胞上组成性表达。为了确定CD6组织特异性表达的分子基础,我们鉴定了控制人类CD6基因近端调控区域活性的转录因子。无TATA盒的CD6启动子包含多个转录起始位点,其在人类T淋巴细胞中的优先活性依赖于位于高度保守区域内的RUNX和Ets结合位点。RUNX和Ets-1因子分别通过识别-215和-230结合位点来反式激活CD6启动子。染色质免疫沉淀试验表明,RUNX1在体内组成性占据CD6启动子,敲低实验表明CD6 mRNA的稳态水平依赖于RUNX1、RUNX3和Ets-1转录因子的表达。因此,RUNX1/3和Ets1控制人类T淋巴细胞中CD6的表达,从而扩大了参与T细胞激活和分化的T细胞特异性及发育调控的淋巴细胞基因靶点范围。