Dolby T W, Belmont A, Borun T W, Nicolini C
J Cell Biol. 1981 Apr;89(1):78-85. doi: 10.1083/jcb.89.1.78.
The onset of DNA replication normally is coincident with an increase in histone 1 phosphorylation and a relaxation in chromatin structure. In this paper we show that 5 mM theophylline, added 2 h after selective detachment to synchronized HeLa-S-3 cells, delays the onset and reduces the rate of DNA synthesis while theophylline treatment beginning at 8 h has no effect on subsequent DNA synthesis. These actions of theophylline are accompanied by an inhibition of histone 1 phosphorylation and a prevention of the normal relaxation in chromatin structure between G1 and S phases as revealed by image analysis of Feulgen-stained nuclei. The time courses of intracellular cyclic AMP levels, nonhistone protein phosphorylation, and [3H]lysine incorporation are also compared in the same treated and untreated synchronized HeLa cells. Comparison with experiments using 1-beta-D-arabinofuranosylcytosine (Ara-C) shows that the above phenomena are not a direct result of inhibition of DNA synthesis. We interpret our results as evidence that the associations between histone 1 phosphorylation, chromatin relaxation, and the onset of DNA synthesis are temporally and causally related.
DNA复制的起始通常与组蛋白1磷酸化的增加以及染色质结构的松弛同时发生。在本文中,我们表明,在选择性脱离后2小时向同步化的HeLa-S-3细胞中添加5 mM茶碱,会延迟DNA合成的起始并降低其速率,而在8小时开始的茶碱处理对随后的DNA合成没有影响。如通过对福尔根染色的细胞核进行图像分析所揭示的,茶碱的这些作用伴随着组蛋白1磷酸化的抑制以及G1期和S期之间染色质结构正常松弛的预防。在相同处理和未处理的同步化HeLa细胞中,还比较了细胞内环磷酸腺苷水平、非组蛋白磷酸化和[3H]赖氨酸掺入的时间进程。与使用1-β-D-阿拉伯呋喃糖基胞嘧啶(Ara-C)的实验比较表明,上述现象不是DNA合成抑制的直接结果。我们将我们的结果解释为组蛋白1磷酸化、染色质松弛和DNA合成起始之间的关联在时间和因果关系上相关的证据。