Nelson David M, Ye Xiaofen, Hall Caitlin, Santos Hidelita, Ma Tianlin, Kao Gary D, Yen Timothy J, Harper J Wade, Adams Peter D
Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111, USA.
Mol Cell Biol. 2002 Nov;22(21):7459-72. doi: 10.1128/MCB.22.21.7459-7472.2002.
DNA and histone synthesis are both triggered at the beginning of S phase by cyclin/cdk2 activity. Previous studies showed that inhibition of DNA synthesis with hydroxyurea or cytosine arabinoside (AraC) triggers a concerted repression of histone synthesis, indicating that sustained histone synthesis depends on continued DNA synthesis. Here we show that ectopic expression of HIRA, the likely human ortholog of two cell cycle-regulated repressors of histone gene transcription in yeast (Hir1p and Hir2p), represses transcription of histones and that this, in turn, triggers a concerted block of DNA synthesis. Thus, in mammalian cells sustained DNA synthesis and histone synthesis are mutually dependent on each other during S phase. Although cyclin/cdk2 activity drives activation of both DNA and histone synthesis at the G1/S transition of cycling cells, concerted repression of DNA or histone synthesis in response to inhibition of either one of these is not accompanied by prolonged inhibition of cyclin A/cdk2 or E/cdk2 activity. Therefore, during S phase coupling of DNA and histone synthesis occurs, at least in part, through a mechanism that is independent of cyclin/cdk2 activity. Coupling of DNA and histone synthesis in S phase presumably contributes to the prompt and orderly assembly of newly replicated DNA into chromatin.
DNA和组蛋白的合成在S期开始时均由细胞周期蛋白/周期蛋白依赖性激酶2(cyclin/cdk2)的活性触发。先前的研究表明,用羟基脲或阿糖胞苷(AraC)抑制DNA合成会引发组蛋白合成的协同抑制,这表明持续的组蛋白合成依赖于持续的DNA合成。在此我们表明,HIRA的异位表达(HIRA可能是酵母中组蛋白基因转录的两个细胞周期调节抑制因子(Hir1p和Hir2p)的人类直系同源物)会抑制组蛋白的转录,进而引发DNA合成的协同阻滞。因此,在哺乳动物细胞中,S期期间持续的DNA合成和组蛋白合成相互依赖。尽管细胞周期蛋白/周期蛋白依赖性激酶2的活性在循环细胞的G1/S转变时驱动DNA和组蛋白合成的激活,但对其中任何一种抑制的反应中,DNA或组蛋白合成的协同抑制并不伴随着细胞周期蛋白A/周期蛋白依赖性激酶2或E/周期蛋白依赖性激酶2活性的长期抑制。因此,在S期,DNA和组蛋白合成的偶联至少部分是通过一种独立于细胞周期蛋白/周期蛋白依赖性激酶2活性的机制发生的。S期DNA和组蛋白合成的偶联可能有助于将新复制的DNA迅速且有序地组装成染色质。