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在具有结构不稳定性的恶性细胞中高效修复 DNA 双链断裂。

Efficient repair of DNA double-strand breaks in malignant cells with structural instability.

机构信息

Genetics Branch, National Cancer Institute, Bethesda, MD 20889-5105, USA.

出版信息

Mutat Res. 2010 Jan 5;683(1-2):115-22. doi: 10.1016/j.mrfmmm.2009.10.016.

Abstract

Aberrant repair of DNA double-strand breaks (DSBs) is thought to be important in the generation of gross chromosomal rearrangements (GCRs). To examine how DNA DSBs might lead to GCRs, we investigated the repair of a single DNA DSB in a structurally unstable cell line. An I-SceI recognition site was introduced into OVCAR-8 cells between a constitutive promoter (EF1alpha) and the Herpes simplex virus thymidine kinase (TK) gene, which confers sensitivity to gancyclovir (GCV). Expression of I-SceI in these cells caused a single DSB. Clones with aberrant repair could acquire resistance to GCV by separation of the EF1alpha promoter from the TK gene, or deletion of either the EF1alpha promoter or the TK gene. All mutations that we identified were interstitial deletions. Treatment of cells with etoposide or bleomycin, agents known to produce DNA DSBs following expression of I-SceI also did not generate GCRs. Because we identified solely interstitial deletions using the aforementioned negative selection system, we developed a positive selection system to produce GCR. A construct containing an I-SceI restriction site immediately followed by a hygromycin phosphotransferase cDNA, with no promoter, was stably integrated into OVCAR-8 cells. DNA DSBs were produced by an I-SceI expression vector. None of the hygromycin resistant clones recovered had linked the hygromycin phosphotransferase cDNA to an endogenous promoter, but had instead captured a portion of the I-SceI expression vector. These results indicate that even in a structurally unstable malignant cell line, the majority of DNA DSBs are repaired by religation of the two broken chromosome ends, without the introduction of a GCR.

摘要

DNA 双链断裂(DSBs)的异常修复被认为在产生染色体结构重排(GCRs)中很重要。为了研究 DNA DSB 如何导致 GCRs,我们研究了在结构不稳定的细胞系中单条 DNA DSB 的修复。在 OVCAR-8 细胞中,在组成型启动子(EF1alpha)和单纯疱疹病毒胸苷激酶(TK)基因之间引入了 I-SceI 识别位点,该基因赋予对更昔洛韦(GCV)的敏感性。这些细胞中 I-SceI 的表达导致单个 DSB。通过将 EF1alpha 启动子与 TK 基因分离,或缺失 EF1alpha 启动子或 TK 基因,具有异常修复的克隆可以获得对 GCV 的抗性。我们鉴定的所有突变都是染色体间缺失。用依托泊苷或博来霉素处理细胞,这些药物在表达 I-SceI 后已知会产生 DNA DSBs,但不会产生 GCRs。由于我们仅使用上述负选择系统鉴定了染色体间缺失,因此我们开发了正选择系统来产生 GCR。含有 I-SceI 限制位点的构建体紧接着是没有启动子的潮霉素磷酸转移酶 cDNA,稳定整合到 OVCAR-8 细胞中。通过 I-SceI 表达载体产生 DNA DSBs。没有一个潮霉素抗性克隆回收的带有连接到内源性启动子的潮霉素磷酸转移酶 cDNA,而是捕获了一部分 I-SceI 表达载体。这些结果表明,即使在结构不稳定的恶性细胞系中,大多数 DNA DSB 也通过两个断裂染色体末端的重新连接修复,而不会引入 GCR。

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