Smekens-Etienne M, Goldstein J, Ooms H A, Dumont J E
Eur J Biochem. 1983 Feb 1;130(2):269-73. doi: 10.1111/j.1432-1033.1983.tb07146.x.
The interferon-induced double-stranded RNA-activated (2'-5')oligo(adenylate) synthetase converts ATP into (2'-5')oligo(adenylate) [(2'-5')oligo(A)] and pyrophosphate. In turn, (2'-5')oligo(A) activates a latent endoribonuclease which cleaves single-stranded RNA. (2'-5')Oligo(A) synthetase activity has been characterized in liver cells of normal and germ-free rats. This enzyme is predominantly nuclear. After partial hepatectomy, (2'-5')oligo(A) synthetase activity decreased rapidly (after 10 h) and markedly to a minimum of 25% of the control after 20 h. This decrease was followed by a slow restoration of the activity. No such change was observed in sham-operated animals. This important decrease of enzymatic activity occurred during the first few hours of liver regeneration (6-24 h). This period corresponds also to the prereplicative and replicative (18-24 h after hepatectomy) phases of DNA. Detailed kinetics indicated that the loss of (2'-5')oligo(A) synthetase activity preceded the onset of the incorporation of tritiated thymidine in DNA and was minimal when the rate of DNA synthesis was maximal. These results and those obtained in culture of cells in vitro are compatible with the hypothesis that the (2'-5')oligo(A) system participates in the negative control of cell proliferation.
干扰素诱导的双链RNA激活的(2'-5')寡腺苷酸合成酶将ATP转化为(2'-5')寡腺苷酸[(2'-5')寡聚腺苷酸]和焦磷酸。反过来,(2'-5')寡聚腺苷酸激活一种潜在的核糖核酸内切酶,该酶可切割单链RNA。已在正常大鼠和无菌大鼠的肝细胞中对(2'-5')寡腺苷酸合成酶活性进行了表征。这种酶主要存在于细胞核中。部分肝切除术后,(2'-5')寡腺苷酸合成酶活性迅速下降(10小时后),并在20小时后显著降至对照值的25%的最低水平。这种下降之后是活性的缓慢恢复。在假手术动物中未观察到这种变化。酶活性的这种重要下降发生在肝再生的最初几个小时(6-24小时)。这个时期也对应于DNA的复制前期和复制期(肝切除术后18-24小时)。详细的动力学表明,(2'-5')寡腺苷酸合成酶活性的丧失先于氚标记的胸腺嘧啶核苷掺入DNA,并且在DNA合成速率最大时降至最低。这些结果以及在体外细胞培养中获得的结果与(2'-5')寡聚腺苷酸系统参与细胞增殖的负调控这一假设相符。