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Illegitimate and homologous recombination in mammalian cells: differential sensitivity to an inhibitor of poly(ADP-ribosylation)

机译:哺乳动物细胞中的非法和同源重组:对聚(ADP-核糖基化)抑制剂的敏感性不同

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We determined the effect of 3-methoxybenzamide (3-MB), a competitive inhibitor of poly(ADP-ribose)polymerase (E.C. 2.4.2.30), on illegitimate and extrachromosomal homologous recombination in mouse Ltk? cells. Cells were transfected with a wild type Herpes thymidine klnase (tk) gene or with two defective tk gene sequences followed by selection for tk-positive colonies. Using a wild type tk gene, colony formation required uptake, integration, and expression of the tk gene. Using defective tk genes, colony formation had the additional requirement for homologous recombination to reconstruct a functional tk gene. The presence of non-cytotoxic levels of 3-MB during and after transfection reduced the number of colonies recovered with a wild type tk gene in a dose-dependent manner, with 2 mM 3-MB causing a 10 to 20-fold reduction. 3-MB reduced the number of colonies recovered with defective tk genes only to the same extent as in transfections with a wild type gene. Treatment with 3-methoxybenzoic acid, a non-inhibitory analog of 3-MB, did not reduce the recovery of colonies in any experiment. Similar results were obtained using linear or supercoiled molecules and when defective tk genes were transfected into cells on one or two different DNA molecules. By assaying for transient expression of the tk gene, we found that 3-MB did not Inhibit uptake or expression of the tk gene. We conclude that poly(ADP-ribosylation) plays a role in random integration (illegitimate recombination) of DNA but does not play an important role in extrachromosomal homologous recombination, demonstrating that these two recombination pathways in cultured mouse fibroblasts are biochemically distinct.
机译:我们确定了竞争性的聚(ADP-核糖)聚合酶抑制剂(EC 2.4.2.30)3-甲氧基苯甲酰胺(3-MB)对小鼠Ltk ?细胞中非法和染色体外同源重组的影响。用野生型疱疹胸苷激酶(tk)基因或两个有缺陷的tk基因序列转染细胞,然后选择tk阳性菌落。使用野生型tk基因,集落形成需要tk基因的摄取,整合和表达。使用有缺陷的tk基因,菌落形成对同源重组具有额外的要求,以重建功能性tk基因。转染过程中和转染后3-MB的非细胞毒性水平的存在以剂量依赖性方式减少了野生型tk基因回收的菌落数量,其中2 mM 3-MB引起了10至20倍的减少。 3-MB减少了用缺陷性tk基因回收的菌落数量,其降低程度仅与野生型基因转染时相同。在任何实验中,用3-甲氧基苯甲酸(一种3-MB的非抑制性类似物)处理都不会降低菌落的回收率。使用线性或超螺旋分子以及将有缺陷的tk基因转染到一个或两个不同DNA分子的细胞中时,也获得了相似的结果。通过检测tk基因的瞬时表达,我们发现3-MB不会抑制tk基因的摄取或表达。我们得出的结论是,聚(ADP-核糖基化)在DNA的随机整合(非法重组)中发挥作用,但在染色体外同源重组中不发挥重要作用,这表明培养的小鼠成纤维细胞中的这两种重组途径在生化上是不同的。

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