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乳糖阻遏蛋白可在动物细胞中调控来自含有乳糖操纵子的杂交SV40早期启动子的基因表达。

lac repressor can regulate expression from a hybrid SV40 early promoter containing a lac operator in animal cells.

作者信息

Brown M, Figge J, Hansen U, Wright C, Jeang K T, Khoury G, Livingston D M, Roberts T M

出版信息

Cell. 1987 Jun 5;49(5):603-12. doi: 10.1016/0092-8674(87)90536-8.

Abstract

The E. coli lac operator and repressor were adapted for function in mammalian cells. Plasmids containing an SV40 early region (pSVlacO) or a chloramphenicol acetyl transferase gene (pSVlacOCAT) linked to a hybrid SV40 early promoter bearing a lac operator were tested for function. Identical plasmids lacking an operator (pX-8 and pX-8CAT) were controls. In vitro, early transcription from pSVlacO, but not from pX-8, was inhibited by lac repressor, and repression was overcome by IPTG. Repression of large T synthesis or CAT activity occurred in vivo only when the respective operator-containing plasmid was cotransfected with a plasmid encoding lac repressor, or when the recipient cells stably synthesized lac repressor. IPTG substantially relieved repression in both cases. CAT enzyme repression was paralleled by a decrease in CAT mRNA abundance. Thus regulatory elements of the lac operon function physiologically in mammalian cells.

摘要

大肠杆菌乳糖操纵子及其阻遏蛋白被改造以在哺乳动物细胞中发挥功能。对含有与带有乳糖操纵子的杂交SV40早期启动子相连的SV40早期区域(pSVlacO)或氯霉素乙酰转移酶基因(pSVlacOCAT)的质粒进行了功能测试。缺少操纵子的相同质粒(pX - 8和pX - 8CAT)作为对照。在体外,乳糖阻遏蛋白抑制了pSVlacO的早期转录,但不抑制pX - 8的转录,IPTG可解除这种抑制。只有当各自含操纵子的质粒与编码乳糖阻遏蛋白的质粒共转染,或者当受体细胞稳定合成乳糖阻遏蛋白时,体内才会发生大T合成或CAT活性的抑制。在这两种情况下,IPTG都能显著缓解抑制作用。CAT酶的抑制伴随着CAT mRNA丰度的降低。因此,乳糖操纵子的调控元件在哺乳动物细胞中具有生理功能。

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