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有丝分裂中新颖的 DNA 损伤检查点:有丝分裂 DNA 损伤会在各种癌细胞中诱导无细胞分裂的再复制。

Novel DNA damage checkpoint in mitosis: Mitotic DNA damage induces re-replication without cell division in various cancer cells.

机构信息

World Class University Research Program, Department of Nanobiomedical Science, Dankook University, 29 Anseo-Dong, Cheonan 330-714, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2012 Jul 6;423(3):593-9. doi: 10.1016/j.bbrc.2012.06.023. Epub 2012 Jun 13.

Abstract

DNA damage induces multiple checkpoint pathways to arrest cell cycle progression until damage is repaired. In our previous reports, when DNA damage occurred in prometaphase, cells were accumulated in 4 N-DNA G1 phase, and mitosis-specific kinases were inactivated in dependent on ATM/Chk1 after a short incubation for repair. We investigated whether or not mitotic DNA damage causes cells to skip-over late mitotic periods under prolonged incubation in a time-lapse study. 4 N-DNA-damaged cells re-replicated without cell division and accumulated in 8 N-DNA content, and the activities of apoptotic factors were increased. The inhibition of DNA replication reduced the 8 N-DNA cell population dramatically. Induction of replication without cell division was not observed upon depletion of Chk1 or ATM. Finally, mitotic DNA damage induces mitotic slippage and that cells enter G1 phase with 4 N-DNA content and then DNA replication is occurred to 8 N-DNA content before completion of mitosis in the ATM/Chk1-dependent manner, followed by caspase-dependent apoptosis during long-term repair.

摘要

DNA 损伤诱导多种检查点途径来阻止细胞周期进程,直到损伤得到修复。在我们之前的报告中,当 DNA 损伤发生在前期时,细胞在 4N-DNA G1 期积累,并且在短时间孵育修复后,有丝分裂特异性激酶依赖于 ATM/Chk1 失活。我们在延时研究中研究了长时间孵育是否会导致有丝分裂 DNA 损伤使细胞跳过晚期有丝分裂期。4N-DNA 损伤的细胞在没有细胞分裂的情况下重新复制,并积累了 8N-DNA 含量,凋亡因子的活性增加。DNA 复制的抑制显著减少了 8N-DNA 细胞群体。在耗尽 Chk1 或 ATM 时,没有观察到无细胞分裂的复制诱导。最后,有丝分裂 DNA 损伤诱导有丝分裂滑溜,细胞进入 4N-DNA 含量的 G1 期,然后在 ATM/Chk1 依赖性方式下进行 DNA 复制到 8N-DNA 含量,然后在长期修复过程中发生 caspase 依赖性凋亡。

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