Lee Gap Ryol, Fields Patrick E, Griffin Thomas J, Flavell Richard A
Section of Immunobiology, Yale University School of Medicine, Yale University, New Haven, CT 06520, USA.
Immunity. 2003 Jul;19(1):145-53. doi: 10.1016/s1074-7613(03)00179-1.
The Th2 cytokine genes IL4, IL5, and IL13 are clustered and expressed in a cell lineage-specific manner. We investigated the global locus-specific regulation of these genes using BAC transgenic mice containing the murine Th2 cytokine cluster carrying an IL4 promoter-luciferase reporter. IL4 promoter activity in effector CD4 T cells from these transgenic mice was strong, Th2 specific, and copy number dependent, suggesting the presence of an LCR in the locus. The production of IL4 and IL13, but not IL5, by these cells was also copy number dependent. Deletion analysis defined a 25 kb fragment in the RAD50 gene as the region containing the LCR activity. Expression of the IL4 promoter-luciferase reporter was transactivated by GATA-3 irrespective of position in the locus, suggesting the global nature of this regulation. The LCR itself, however, does not respond directly to GATA-3.
Th2细胞因子基因IL4、IL5和IL13成簇存在,并以细胞谱系特异性方式表达。我们使用携带含有IL4启动子-荧光素酶报告基因的小鼠Th2细胞因子簇的BAC转基因小鼠,研究了这些基因的全基因组位点特异性调控。来自这些转基因小鼠的效应CD4 T细胞中,IL4启动子活性很强,具有Th2特异性且依赖拷贝数,提示该位点存在一个LCR。这些细胞产生IL4和IL13,但不产生IL5,也依赖拷贝数。缺失分析确定RAD50基因中的一个25 kb片段为含有LCR活性的区域。无论在基因座中的位置如何,IL4启动子-荧光素酶报告基因的表达都被GATA-3反式激活,提示这种调控具有全局性。然而,LCR本身并不直接对GATA-3作出反应。