Ranjith-Kumar C T, Gutshall Les, Kim Min-Ju, Sarisky Robert T, Kao C Cheng
Department of Biology, Indiana University, 1001 E. Third Street, Bloomington, IN 47405, USA.
J Virol. 2002 Dec;76(24):12526-36. doi: 10.1128/jvi.76.24.12526-12536.2002.
RNA-dependent RNA polymerases (RdRps) that initiate RNA synthesis by a de novo mechanism should specifically recognize the template initiation nucleotide, T1, and the substrate initiation nucleotide, the NTPi. The RdRps from hepatitis C virus (HCV), bovine viral diarrhea virus (BVDV), and GB virus-B all can initiate RNA synthesis by a de novo mechanism. We used RNAs and GTP analogs, respectively, to examine the use of the T1 nucleotide and the initiation nucleotide (NTPi) during de novo initiation of RNA synthesis. The effects of the metal ions Mg(2+) and Mn(2+) on initiation were also analyzed. All three viral RdRps require correct base pairing between the T1 and NTPi for efficient RNA synthesis. However, each RdRp had some distinct tolerances for modifications in the T1 and NTPi. For example, the HCV RdRp preferred an NTPi lacking one or more phosphates regardless of whether Mn(2+) was present or absent, while the BVDV RdRp efficiently used GDP and GMP for initiation of RNA synthesis only in the presence of Mn(2+). These and other results indicate that although the three RdRps share a common mechanism of de novo initiation, each has distinct preferences.
通过从头合成机制起始RNA合成的RNA依赖性RNA聚合酶(RdRps)应特异性识别模板起始核苷酸T1和底物起始核苷酸NTPi。丙型肝炎病毒(HCV)、牛病毒性腹泻病毒(BVDV)和GB病毒B的RdRps都可以通过从头合成机制起始RNA合成。我们分别使用RNA和GTP类似物来研究RNA合成从头起始过程中T1核苷酸和起始核苷酸(NTPi)的使用情况。还分析了金属离子Mg(2+)和Mn(2+)对起始的影响。所有三种病毒RdRps都需要T1和NTPi之间正确的碱基配对才能进行有效的RNA合成。然而,每种RdRp对T1和NTPi修饰都有一些不同的耐受性。例如,无论是否存在Mn(2+) ,HCV RdRp都更喜欢缺少一个或多个磷酸基团的NTPi,而BVDV RdRp仅在存在Mn(2+)时才能有效地使用GDP和GMP起始RNA合成。这些以及其他结果表明,尽管这三种RdRps具有共同的从头起始机制,但每种都有不同的偏好。