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紫外线敏感型中国仓鼠卵巢细胞(CHO)突变体与着色性干皮病成纤维细胞之间的遗传互补作用。

Genetic complementation between UV-sensitive CHO mutants and xeroderma pigmentosum fibroblasts.

作者信息

Thompson L H, Mooney C L, Brookman K W

出版信息

Mutat Res. 1985 Jun-Jul;150(1-2):423-9. doi: 10.1016/0027-5107(85)90139-3.

Abstract

The purpose of this study was to determine the feasibility of doing complementation analysis between DNA-repair mutants of CHO cells and human fibroblasts based on the recovery of hybrid cells resistant to DNA damage. Two UV-sensitive CHO mutant lines, UV20 and UV41, which belong to different genetic complementation groups, were fused with fibroblasts of xeroderma pigmentosum in various complementation groups. Selection for complementing hybrids was performed using a combination of ouabain to kill the XP cells and mitomycin C to kill the CHO mutants. Because the frequency of viable hybrid clones was generally less than 10(-6) and the frequency of revertants of each CHO mutant was approximately 2 X 10(-7), putative hybrids required verification. The hybrid character of clones was established by testing for the presence of human DNA in a dot-blot procedure. Hybrid clones were obtained from 9 of the 10 different crosses involving 5 complementation groups of XP cells. The 4 attempted crosses with 2 other XP groups yielded no hybrid colonies. Thus, a definitive complementation analysis was not possible. Hybrids were evaluated for their UV resistance using a rapid assay that measures differential cytotoxicity (DC). All 9 hybrids were more resistant than the parental mutant CHO and XP cells, indicating that in each case complementation of the CHO repair defect by a human gene had occurred. 3 hybrids were analyzed for their UV-radiation survival curves and shown to be much more resistant that the CHO mutants but less resistant than normal CHO cells. With 2 of these hybrids, sensitive subclones, which had presumably lost the complementing gene, were found to have similar sensitivity to the parental CHO mutants. We conclude that the extremely low frequency of viable hybrids in this system limits the usefulness of the approach. The possibility remains that each of the nonhybridizing XP strains could be altered in the same locus as one of the CHO mutants.

摘要

本研究的目的是基于对DNA损伤具有抗性的杂交细胞的恢复情况,确定在CHO细胞和人成纤维细胞的DNA修复突变体之间进行互补分析的可行性。将属于不同遗传互补组的两个对紫外线敏感的CHO突变株系UV20和UV41与不同互补组的着色性干皮病成纤维细胞进行融合。使用哇巴因杀死XP细胞和丝裂霉素C杀死CHO突变体的组合来选择互补杂种。由于存活杂交克隆的频率通常低于10^(-6),且每个CHO突变体的回复体频率约为2×10^(-7),因此推定的杂种需要进行验证。通过斑点印迹法检测人DNA的存在来确定克隆的杂交特性。从涉及5个XP细胞互补组的10个不同杂交组合中的9个获得了杂交克隆。与另外2个XP组进行的4次尝试杂交未产生杂交菌落。因此,无法进行明确的互补分析。使用一种测量差异细胞毒性(DC)的快速检测方法评估杂种的紫外线抗性。所有9个杂种比亲本突变CHO细胞和XP细胞更具抗性,表明在每种情况下,人基因都对CHO修复缺陷进行了互补。对3个杂种的紫外线辐射存活曲线进行了分析,结果表明它们比CHO突变体更具抗性,但比正常CHO细胞抗性低。在其中2个杂种中,发现可能失去互补基因的敏感亚克隆对亲本CHO突变体具有相似的敏感性。我们得出结论,该系统中存活杂种的极低频率限制了该方法的实用性。非杂交XP菌株中的每一个都有可能在与其中一个CHO突变体相同的位点发生改变。

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