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EcoRI 限制性内切酶对 CHO 突变体 EM9 及其亲本系 AA8 的染色体畸变诱导作用:电穿孔实验

Induction of chromosomal aberrations in the CHO mutant EM9 and its parental line AA8 by EcoRI restriction endonuclease: electroporation experiments.

作者信息

Cortés F, Ortiz T

机构信息

Department of Cell Biology, Faculty of Biology, Seville, Spain.

出版信息

Mutat Res. 1991 Jan;246(1):221-6. doi: 10.1016/0027-5107(91)90125-8.

Abstract

EcoRI restriction endonuclease (RE), which produces cohesive-ended double-strand breaks (dsb) in DNA, was tested in the ethyl methanesulfonate- and X-ray-sensitive CHO mutant EM9 and its parental cell strain AA8 for its chromosomal aberration-inducing effect. The RE was efficiently introduced by electroporation into AA8 cells, while the mutant cells showed a very high sensitivity to electroporation, which consistently resulted in cell death. Nevertheless, the incubation of EM9 cells in the presence of EcoRI, without electroporation, was sufficient to induce about three times the chromosome damage observed in the electroporated parental cell line AA8 for any given dose of the RE.

摘要

在DNA中产生粘性末端双链断裂(dsb)的EcoRI限制性内切酶(RE),在对甲磺酸乙酯和X射线敏感的CHO突变体EM9及其亲本细胞系AA8中,测试了其诱导染色体畸变的作用。通过电穿孔将RE有效地导入AA8细胞,而突变细胞对电穿孔表现出非常高的敏感性,这始终导致细胞死亡。然而,在没有电穿孔的情况下,在EcoRI存在下培养EM9细胞,对于任何给定剂量的RE,足以诱导出在电穿孔的亲本细胞系AA8中观察到的约三倍的染色体损伤。

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