Kaz'min S D, Smirnova I A
R.E. Kavetsky Institute for Oncology Problems, Ukrainian SSR, Academy of Sciences, Kiev.
Folia Biol (Praha). 1989;35(3):143-51.
Using ascites tumour cells (Ehrlich carcinoma, plasmacytoma MOPS-21, leukaemia P-388, lympholeukaemia NK/Ly) and bone marrow cells from normal rats, we have demonstrated that transcription of a gene coding for the 35S RNA can be regulated via alteration of the Na+/K+ ratio in the cells. The 35S RNA was transcriptionally active within the range 1 less than or equal to Na+/K+ less than 3 but was switched off at Na+/K+ less than 1. In synchronized Ehrlich carcinoma cells this gene was activated in the early phases of the cell cycle, when the Na+/K+ ratio in the cells exceeded 1. It was concluded that so-called cationic mechanism of regulation of transcription determines the time and sequence of stimulation of certain genes during the course of the cell cycle and that it accounts for transcription of normally repressed genes as a result of malignant transformation.
利用腹水肿瘤细胞(艾氏癌、骨髓瘤MOPS - 21、白血病P - 388、淋巴细胞白血病NK/Ly)以及正常大鼠的骨髓细胞,我们已经证明,编码35S RNA的基因转录可通过改变细胞内的Na⁺/K⁺比值来调控。35S RNA在1≤Na⁺/K⁺<3的范围内具有转录活性,但在Na⁺/K⁺<1时则关闭。在同步化的艾氏癌细胞中,该基因在细胞周期的早期阶段被激活,此时细胞内的Na⁺/K⁺比值超过1。得出的结论是,所谓的转录调控阳离子机制决定了细胞周期过程中某些基因刺激的时间和顺序,并且它解释了恶性转化导致正常情况下被抑制的基因的转录。