Altschmied J, Muller M, Baniahmad A, Steiner C, Renkawitz R
Genzentrum, Max-Planck-Institut für Biochemie, Martinsried, FRG.
Nucleic Acids Res. 1989 Jul 11;17(13):4975-91. doi: 10.1093/nar/17.13.4975.
Expression of the lysozyme gene is a marker for the differentiation of macrophages, lysozyme transcription being gradually increased during maturation. We have analyzed the fine structure and function of two macrophage-specific enhancer elements of the chicken lysozyme gene (E-2.7 kb and E-0.2 kb). Both increase their activities upon LPS induction, both contain multiple binding sites for similar or identical nuclear factors and both can be divided into two functional modules. For the E-0.2 kb enhancer we found a synergistic activity of the modules to be dependent on their distance. Binding sites for nuclear proteins within enhancer E-0.2 kb overlap substantially with the previously identified progesterone/glucocorticoid receptor binding site, which is required for steroid induction of lysozyme transcription in the oviduct.
溶菌酶基因的表达是巨噬细胞分化的一个标志,溶菌酶转录在成熟过程中逐渐增加。我们分析了鸡溶菌酶基因的两个巨噬细胞特异性增强子元件(E-2.7 kb和E-0.2 kb)的精细结构和功能。两者在LPS诱导后活性均增强,均含有多个相似或相同核因子的结合位点,且均可分为两个功能模块。对于E-0.2 kb增强子,我们发现模块的协同活性取决于它们之间的距离。增强子E-0.2 kb内核蛋白的结合位点与先前鉴定的孕酮/糖皮质激素受体结合位点有很大重叠,该位点是输卵管中溶菌酶转录的类固醇诱导所必需的。