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用于真核细胞中基因表达诱导性反式激活的遗传开关的构建。

Construction of a genetic switch for inducible trans-activation of gene expression in eucaryotic cells.

作者信息

Rhode S L

出版信息

J Virol. 1987 May;61(5):1448-56. doi: 10.1128/JVI.61.5.1448-1456.1987.

Abstract

The cotransfection of selectable marker genes and the gene for the nonstructural proteins NS1 and NS2 of the autonomous parvovirus H-1 failed to produce cell lines that constitutively expressed NS1. A plasmid, pP38NS1cat, was constructed that expressed the NS1-NS2 gene from the H-1 P38 coat protein promoter in place of the natural P4 promoter. The P38 promoter is constitutively weak and is trans-activated by NS1. Stable cell lines were isolated that contained pP38NS1cat that was constitutively silent, but inducible with exogenous NS1 by superinfection or by treatment with sodium butyrate. The cells that were induced for this self-stimulatory genetic circuit did not remain in the culture, suggesting that expression of NS1-NS2 is cytotoxic or that the expression is not sustained. The properties of these cell lines and an example of the construction of a cell line inducible for expression of the viral coat protein gene and the bacterial gene for chloramphenicol acetyltransferase (cat) are described.

摘要

共转染自主细小病毒H-1的选择标记基因以及非结构蛋白NS1和NS2的基因未能产生持续表达NS1的细胞系。构建了一个质粒pP38NS1cat,其从H-1 P38衣壳蛋白启动子表达NS1-NS2基因,取代了天然的P4启动子。P38启动子组成性较弱且被NS1反式激活。分离出含有pP38NS1cat的稳定细胞系,该细胞系组成性沉默,但通过超感染或丁酸钠处理可被外源性NS1诱导。因这种自我刺激遗传回路而被诱导的细胞并未留在培养物中,这表明NS1-NS2的表达具有细胞毒性或者该表达不能持续。描述了这些细胞系的特性以及构建一个可诱导表达病毒衣壳蛋白基因和氯霉素乙酰转移酶(cat)细菌基因的细胞系的实例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a788/254122/a70a423b4a55/jvirol00096-0161-a.jpg

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