Hovanessian A G
CNRS, Institut Pasteur, 75015 Paris, France.
J Interferon Res. 1991 Aug;11(4):199-205. doi: 10.1089/jir.1991.11.199.
Treatment of cells with interferon (IFN) results in the induction of two double-stranded RNA (dsRNA)-activated enzymes: a specific protein kinase and 2'-5' linked oligoadenylate [pppA(2'p5'A)n referred to as 2-5A] synthetases. The protein kinase, when activated by dsRNA, becomes autophosphorylated and catalyzes and phosphorylation of the protein synthesis initiation factor, eIF2. The 2-5A synthetases, when activated by dsRNA, form 2-5A molecules capable of activating a latent endoribonuclease that degrades RNA. By inhibiting initiation of protein synthesis or by degrading of RNA, these enzymes play key roles in two independent pathways that regulate overall protein synthesis.
用干扰素(IFN)处理细胞会诱导产生两种双链RNA(dsRNA)激活酶:一种特异性蛋白激酶和2'-5'连接的寡聚腺苷酸[pppA(2'p5'A)n,称为2-5A]合成酶。该蛋白激酶在被dsRNA激活后会发生自身磷酸化,并催化蛋白质合成起始因子eIF2的磷酸化。2-5A合成酶在被dsRNA激活后,会形成能够激活一种潜伏性核糖核酸内切酶的2-5A分子,该核糖核酸内切酶可降解RNA。通过抑制蛋白质合成的起始或通过降解RNA,这些酶在调节整体蛋白质合成的两条独立途径中发挥关键作用。