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中国仓鼠卵巢X射线敏感突变细胞xrs 5和xrs 6的细胞遗传学特征。VII. 使用早熟染色体凝聚技术对X射线照射的野生型CHO-K1和xrs突变细胞进行互补分析。

Cytogenetical characterization of Chinese hamster ovary X-ray-sensitive mutant cells xrs 5 and xrs 6. VII. Complementation analysis of X-irradiated wild-type CHO-K1 and xrs mutant cells using the premature chromosome condensation technique.

作者信息

Darroudi F, Natarajan A T

机构信息

Department of Radiation Genetics and Chemical Mutagenesis, State University of Leiden, The Netherlands.

出版信息

Mutat Res. 1989 Aug;213(2):249-55. doi: 10.1016/0027-5107(89)90157-7.

DOI:10.1016/0027-5107(89)90157-7
PMID:2761559
Abstract

The complementation effect of wild-type CHO-K1 and xrs mutants after fusion, as judged by the frequencies of X-ray-induced G1 and G2 premature chromosome condensation (PCC), was studied. For induction of PCC, X-irradiated interphase cells (G1 and G2) were fused immediately with untreated mitotic cells of the same cell line or with mitotic cells of another line. The frequencies of breaks in G1-PCC, or breaks and chromatid exchanges in G2-PCC were determined and the latter parameter was compared with the frequency of chromosomal aberrations in mitotic cells following G2 irradiation. CHO-K1 cells were capable of complementing the X-ray sensitivity of both xrs 5 and xrs 6 cells. However, full restoration of the repair defect in xrs cells could never be accomplished. The mutants failed to complement each other. In CHO-K1 cells, the incidence of chromosomal aberrations was significantly higher in G2-PCC (2.5-fold) than that observed in mitotic cells at 2.5 h after irradiation. The ratio of the induced frequency of aberrations in G2-PCC to that in mitotic cells was correlated with the degree of repair of DNA double-strand breaks (dsb) and reached almost 1 in xrs 5 cells indicating no repair. In addition the data indicated that, during the period of recovery of CHO-K1 cells, X-ray-induced breaks decreased but exchanges remained at the same level. In contrast, due to a deficiency in rejoining of dsb in xrs mutants, breaks remained open for a long period of time, allowing the formation of additional chromatid exchanges during recovery time.

摘要

通过X射线诱导的G1期和G2期早熟染色体凝集(PCC)频率,研究了野生型CHO-K1和xrs突变体融合后的互补效应。为了诱导PCC,将经X射线照射的间期细胞(G1期和G2期)立即与同一细胞系未经处理的有丝分裂细胞或另一细胞系的有丝分裂细胞融合。测定G1-PCC中的断裂频率,或G2-PCC中的断裂和染色单体交换频率,并将后一参数与G2期照射后有丝分裂细胞中的染色体畸变频率进行比较。CHO-K1细胞能够互补xrs 5和xrs 6细胞的X射线敏感性。然而,xrs细胞修复缺陷的完全恢复从未实现。这些突变体不能相互互补。在CHO-K1细胞中,G2-PCC中的染色体畸变发生率(2.5倍)显著高于照射后2.5小时有丝分裂细胞中的发生率。G2-PCC中诱导的畸变频率与有丝分裂细胞中诱导的畸变频率之比与DNA双链断裂(dsb)的修复程度相关,在xrs 5细胞中几乎达到1,表明没有修复。此外,数据表明,在CHO-K1细胞恢复期间,X射线诱导的断裂减少,但交换保持在相同水平。相反,由于xrs突变体中dsb重新连接的缺陷,断裂长时间保持开放,在恢复期间允许形成额外的染色单体交换。

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