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黄病毒 NS5 甲基转移酶对内源性腺苷的 2'-O 甲基化。

2'-O methylation of internal adenosine by flavivirus NS5 methyltransferase.

机构信息

Novartis Institute for Tropical Diseases, Singapore.

出版信息

PLoS Pathog. 2012;8(4):e1002642. doi: 10.1371/journal.ppat.1002642. Epub 2012 Apr 5.

Abstract

RNA modification plays an important role in modulating host-pathogen interaction. Flavivirus NS5 protein encodes N-7 and 2'-O methyltransferase activities that are required for the formation of 5' type I cap (m(7)GpppAm) of viral RNA genome. Here we reported, for the first time, that flavivirus NS5 has a novel internal RNA methylation activity. Recombinant NS5 proteins of West Nile virus and Dengue virus (serotype 4; DENV-4) specifically methylates polyA, but not polyG, polyC, or polyU, indicating that the methylation occurs at adenosine residue. RNAs with internal adenosines substituted with 2'-O-methyladenosines are not active substrates for internal methylation, whereas RNAs with adenosines substituted with N⁶-methyladenosines can be efficiently methylated, suggesting that the internal methylation occurs at the 2'-OH position of adenosine. Mass spectroscopic analysis further demonstrated that the internal methylation product is 2'-O-methyladenosine. Importantly, genomic RNA purified from DENV virion contains 2'-O-methyladenosine. The 2'-O methylation of internal adenosine does not require specific RNA sequence since recombinant methyltransferase of DENV-4 can efficiently methylate RNAs spanning different regions of viral genome, host ribosomal RNAs, and polyA. Structure-based mutagenesis results indicate that K61-D146-K181-E217 tetrad of DENV-4 methyltransferase forms the active site of internal methylation activity; in addition, distinct residues within the methyl donor (S-adenosyl-L-methionine) pocket, GTP pocket, and RNA-binding site are critical for the internal methylation activity. Functional analysis using flavivirus replicon and genome-length RNAs showed that internal methylation attenuated viral RNA translation and replication. Polymerase assay revealed that internal 2'-O-methyladenosine reduces the efficiency of RNA elongation. Collectively, our results demonstrate that flavivirus NS5 performs 2'-O methylation of internal adenosine of viral RNA in vivo and host ribosomal RNAs in vitro.

摘要

RNA 修饰在调节宿主-病原体相互作用中起着重要作用。黄病毒 NS5 蛋白编码 N-7 和 2'-O 甲基转移酶活性,这些活性对于病毒 RNA 基因组 5' 型 I 帽(m(7)GpppAm)的形成是必需的。在这里,我们首次报道黄病毒 NS5 具有新型的内部 RNA 甲基化活性。西尼罗河病毒和登革热病毒(血清型 4;DENV-4)的重组 NS5 蛋白特异性甲基化 polyA,但不甲基化 polyG、polyC 或 polyU,表明甲基化发生在腺苷残基上。内部腺苷被 2'-O-甲基腺苷取代的 RNA 不是内部甲基化的有效底物,而腺苷被 N⁶-甲基腺苷取代的 RNA 可以被有效地甲基化,这表明内部甲基化发生在腺苷的 2'-OH 位置。质谱分析进一步表明内部甲基化产物是 2'-O-甲基腺苷。重要的是,从 DENV 病毒粒子中纯化的基因组 RNA 含有 2'-O-甲基腺苷。内部腺苷的 2'-O 甲基化不需要特定的 RNA 序列,因为 DENV-4 的重组甲基转移酶可以有效地甲基化跨越病毒基因组、宿主核糖体 RNA 和 polyA 的不同区域的 RNA。基于结构的诱变结果表明,DENV-4 甲基转移酶的 K61-D146-K181-E217 四联体形成内部甲基化活性的活性位点;此外,甲基供体(S-腺苷-L-甲硫氨酸)口袋、GTP 口袋和 RNA 结合位点内的不同残基对于内部甲基化活性至关重要。使用黄病毒复制子和全长 RNA 的功能分析表明,内部甲基化会减弱病毒 RNA 的翻译和复制。聚合酶测定显示内部 2'-O-甲基腺苷会降低 RNA 延伸的效率。总之,我们的结果表明,黄病毒 NS5 在体内对病毒 RNA 的内部腺苷和体外对宿主核糖体 RNA 进行 2'-O 甲基化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd01/3320599/6fe4a9c4d273/ppat.1002642.g001.jpg

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