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首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Isolation and characterization of the chicken m2 acetylcholine receptor promoter region: Induction of gene transcription by leukemia inhibitory factor and ciliary neurotrophic factor
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Isolation and characterization of the chicken m2 acetylcholine receptor promoter region: Induction of gene transcription by leukemia inhibitory factor and ciliary neurotrophic factor

机译:鸡m2乙酰胆碱受体启动子区的分离和鉴定:白血病抑制因子和睫状神经营养因子诱导基因转录

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摘要

We have isolated the promoter region and determined the start sites of transcription for the gene encoding the chicken m2 (cm2) muscarinic acetylcholine receptor. Transfection experiments, using cm2-luciferase re- porter gene constructs, demonstrated that a 789-bp genomic fragment was sufficient to drive high level expression in chicken heart primary cultures, while an additional 1.2-kb region was required for maximal expression in mouse septal/ neuroblastoma (SN56) cells. Treatment of SN56 cells with the cytokines ciliary neurotrophic factor and leukemia inhibitory factor increases expression of endogenous muscarinic acetyl- choline receptors and results in a 4- to 6-fold induction of cm2 promoter driven luciferase expression. We have mapped a region of the cm2 promoter that is necessary for induction by cytokines.
机译:我们已经分离出启动子区域,并确定了编码鸡m2(cm2)毒蕈碱型乙酰胆碱受体的基因的转录起始位点。使用cm2-荧光素酶报告基因构建体进行的转染实验表明,一个789-bp的基因组片段足以驱动鸡心原代培养物中的高水平表达,而在小鼠中隔/小鼠中最大表达则需要一个额外的1.2-kb区域。神经母细胞瘤(SN56)细胞。用细胞因子睫状神经营养因子和白血病抑制因子处理SN56细胞会增加内源性毒蕈碱型乙酰胆碱受体的表达,并导致4至6倍诱导cm2启动子驱动的荧光素酶表达。我们已经绘制了由细胞因子诱导所必需的cm2启动子区域。

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