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Lysozyme gene activity in chicken macrophages is controlled by positive and negative regulatory elements.

机译:鸡巨噬细胞中的溶菌酶基因活性受正调控元件和负调控元件控制。

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摘要

The chicken lysozyme gene is constitutively active in macrophages and under the control of steroid hormones in the oviduct. To investigate which DNA elements are involved in the control of its expression in macrophages we performed transient DNA transfer experiments with two different types of plasmids: 5'-deletion mutants of the upstream region of the chicken lysozyme gene and different fragments from this area in front of the thymidine kinase promoter (herpes simplex virus), each placed in front of the CAT (chloramphenicol acetyl transferase) coding sequence. Two enhancers (E-2.7 kb and E-0.2 kb) were characterized. They are active in macrophages, but not in chicken fibroblasts. Furthermore a negative element (N-2.4 kb) was identified, which is active in fibroblasts and promyelocytes, but not in mature macrophages. The combined action of all three elements contributes to the observed lysozyme gene activities: no activity in fibroblasts, moderate activity in promyelocytes and high activity in mature macrophages.
机译:鸡溶菌酶基因在巨噬细胞中具有组成性活性,并且在输卵管中类固醇激素的控制下。为了研究哪些DNA元件参与了其在巨噬细胞中的表达控制,我们使用两种不同类型的质粒进行了瞬时DNA转移实验:鸡溶菌酶基因上游区域的5'-缺失突变体以及该区域前面的不同片段胸苷激酶启动子(单纯疱疹病毒)的基因,每个都位于CAT(氯霉素乙酰基转移酶)编码序列的前面。表征了两种增强子(E-2.7 kb和E-0.2 kb)。它们在巨噬细胞中有活性,但在鸡成纤维细胞中没有活性。此外,鉴定出一种负性元件(N-2.4 kb),其在成纤维细胞和早幼粒细胞中有活性,而在成熟的巨噬细胞中则无活性。所有这三种元素的共同作用有助于观察到的溶菌酶基因活性:成纤维细胞无活性,早幼粒细胞有中等活性,成熟巨噬细胞有高活性。

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