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通过稳定表达Sh ble基因产生的对博来霉素抗生素的抗性并不能完全抑制博来霉素在人类细胞中诱导的DNA切割。

Resistance to the antibiotic Zeocin by stable expression of the Sh ble gene does not fully suppress Zeocin-induced DNA cleavage in human cells.

作者信息

Oliva-Trastoy Manel, Defais Martine, Larminat Florence

机构信息

IPBS, UMR 5089 CNRS, 205 Route de Narbonne, 31077 Toulouse, France.

出版信息

Mutagenesis. 2005 Mar;20(2):111-4. doi: 10.1093/mutage/gei016. Epub 2005 Mar 8.

Abstract

Zeocin is a member of the bleomycin/phleomycin family of antibiotics, known to bind and cleave DNA. We established human SK-OV-3 cells that stably express the Zeocin resistance gene (Sh ble) using an ecdysone-inducible mammalian expression system. Surprisingly, our results demonstrated that Zeocin, added in the culture medium to maintain the expression of the ecdysone receptor, was responsible for the formation of DNA strand breaks in the recombinant cells. This suggests that the Zeocin is not completely detoxified and is still able to cleave DNA, despite the stable expression of the Sh ble gene in the recombinant clones. Our study indicates that one needs to be very cautious in the interpretation of data involving stable cell lines selected with Zeocin.

摘要

博来霉素是博来霉素/腐草霉素类抗生素的一员,已知其能结合并切割DNA。我们使用蜕皮激素诱导型哺乳动物表达系统建立了稳定表达博来霉素抗性基因(Sh ble)的人SK-OV-3细胞。令人惊讶的是,我们的结果表明,添加到培养基中以维持蜕皮激素受体表达的博来霉素,是重组细胞中DNA链断裂形成的原因。这表明,尽管重组克隆中Sh ble基因稳定表达,但博来霉素并未完全解毒,仍能够切割DNA。我们的研究表明,在解释涉及用博来霉素筛选的稳定细胞系的数据时需要非常谨慎。

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