Smith R E, Furuichi Y
J Biol Chem. 1982 Jan 10;257(1):485-94.
Two structurally different classes of oligonucleotides accumulate in vitro in cytoplasmic polyhedrosis virus (CPV) transcription mixtures in molar excess as compared to the completed RNA products. The first class consists of oligonucleotides which correspond to the 5'-terminal sequence of the virus mRNAs (referred to as initiator oligonucleotides). The major species of initiator oligonucleotides are (p)ppApG and (p)ppApGpN together with smaller amounts of homologous capped structures (Furuichi, Y. (1981) J. Biol. Chem. 256, 483-493). In addition to initiator oligonucleotides, CPV transcription mixtures yielded a second new class of compounds which were radiolabeled by [alpha-32P]GTP and resistant to phosphatase digestion. Their structures were identified as G(5')pppp(5')A, G(5')pppp(5')C, G(5')pppp(5')G, and G(5')pppp(5')U. With the exception of G(5')pppp(5')G, these compounds have not been observed previously. The mechanism of synthesis of these unique compounds was elucidated as pppG + pppN leads to GppppN + PPi. The reaction resembles, in principle, a guanylylation reaction which occurs during cap formation in CPV and other eukaryotic mRNA syntheses. It is likely that these compounds are formed in a similar way by a condensation reaction involving a viral guanylyltransferase-pG intermediate complex and ribonucleoside triphosphate. When the amounts of G(5')pppp(5')N were measured, it was found that G(5')pppp(5')N reached maximum concentrations (0.4 to 0.7 microM) shortly after the onset of RNA synthesis (1 h) and these levels were maintained or diminished gradually. By contrast, mRNA and (p)ppApG were continuously synthesized. The relative molar ratios of total G(5')pppp(5')N and (p)ppApG versus mRNA were comparable (74:24:1 and 30:27:1 during 1 to 4 h transcription, respectively). The results imply that these unusual compounds G(5')pppp(5')N as well as initiator oligonucleotides may be produced reiteratively during initiation when RNA chain elongation and capping are uncoupled.
与完整的RNA产物相比,两类结构不同的寡核苷酸以摩尔过量的形式在体外细胞质多角体病毒(CPV)转录混合物中积累。第一类由与病毒mRNA 5'末端序列相对应的寡核苷酸组成(称为起始寡核苷酸)。起始寡核苷酸的主要种类是(p)ppApG和(p)ppApGpN,还有少量同源的加帽结构(古市洋一(1981年)《生物化学杂志》256卷,483 - 493页)。除了起始寡核苷酸外,CPV转录混合物还产生了第二类新的化合物,这些化合物被[α - 32P]GTP放射性标记且对磷酸酶消化有抗性。它们的结构被鉴定为G(5')pppp(5')A、G(5')pppp(5')C、G(5')pppp(5')G和G(5')pppp(5')U。除了G(5')pppp(5')G外,这些化合物以前未曾被观察到。这些独特化合物的合成机制被阐明为pppG + pppN生成GppppN + PPi。该反应原则上类似于CPV和其他真核mRNA合成中帽形成过程中发生的鸟苷酸化反应。这些化合物很可能是通过涉及病毒鸟苷酸转移酶 - pG中间复合物和核糖核苷三磷酸的缩合反应以类似方式形成的。当测量G(5')pppp(5')N的量时,发现G(5')pppp(5')N在RNA合成开始后不久(1小时)达到最大浓度(0.4至0.7微摩尔),并且这些水平保持不变或逐渐降低。相比之下,mRNA和(p)ppApG是持续合成的。总G(5')pppp(5')N和(p)ppApG与mRNA的相对摩尔比是相当的(在1至4小时转录期间分别为74:24:1和30:27:1)。结果表明,当RNA链延伸和加帽解偶联时,这些不寻常的化合物G(5')pppp(5')N以及起始寡核苷酸可能在起始过程中反复产生。