Zheng S A, McElwain C M, Taffet S M
Department of Biochemistry and Molecular Biology, S.U.N.Y. Health Science Center, Syracuse 13210.
Biochem Biophys Res Commun. 1991 Feb 28;175(1):48-54. doi: 10.1016/s0006-291x(05)81198-2.
The ability of the promotor/enhancer region of the mouse ornithine decarboxylase gene to respond to various stimuli was studied. This region was subcloned into multiple fragments and these were inserted in front of the chloramphenicol acetyltransferase gene on an expression vector, pBLCAT3. These ODC/CAT constructs were transfected into a mouse macrophage-like cell line, RAW264. The transfected cells were stimulated by bacterial lipopolysaccharide, 8-bromo cAMP or both followed by analysis of chloramphenicol acetyltransferase activity. Optimal inducible chloramphenicol acetyltransferase expression was obtained when sequences from -90 to +12 (with respect to the transcriptional start site) were tested in cells treated with a combination of lipopolysaccharide and 8-bromo cAMP. A putative cyclic AMP response element located at -48 was altered by site-directed mutagenesis but these alterations did not diminish activity in response to stimulation with lipopolysaccharide and 8-bromo cAMP.
对小鼠鸟氨酸脱羧酶基因启动子/增强子区域响应各种刺激的能力进行了研究。该区域被亚克隆为多个片段,并插入到表达载体pBLCAT3上氯霉素乙酰转移酶基因的前面。将这些ODC/CAT构建体转染到小鼠巨噬细胞样细胞系RAW264中。用细菌脂多糖、8-溴环磷腺苷或两者刺激转染细胞,随后分析氯霉素乙酰转移酶活性。当在经脂多糖和8-溴环磷腺苷联合处理的细胞中测试从-90至+12(相对于转录起始位点)的序列时,获得了最佳诱导型氯霉素乙酰转移酶表达。位于-48的一个假定的环磷腺苷反应元件通过定点诱变进行了改变,但这些改变并未降低对脂多糖和8-溴环磷腺苷刺激的反应活性。