Biochemical and genetic characterization of dengue virus methyltransferase

被引:87
作者
Dong, Hongping [1 ]
Chang, David C. [1 ]
Xie, Xuping [1 ]
Toh, Ying Xiu [1 ,2 ]
Chung, Ka Yan [1 ,2 ]
Zou, Gang [1 ]
Lescar, Julien [2 ]
Lim, Siew Pheng [1 ]
Shi, Pei-Yong [1 ]
机构
[1] Novartis Inst Trop Dis, Singapore 138670, Singapore
[2] Nanyang Technol Univ, Sch Biol Sci, Singapore 637551, Singapore
关键词
Dengue virus; Methyltransferase; RNA cap methylation; Flavivirus replication; Antiviral target; WEST-NILE-VIRUS; MESSENGER-RNA; CRYSTAL-STRUCTURE; FLAVIVIRUS; NS5; CAP; PROTEIN; DOMAIN; METHYLATION; POLYMERASE;
D O I
10.1016/j.virol.2010.06.039
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We report that dengue virus (DENV) methyltransferase sequentially methylates the guanine N-7 and ribose 2'-O positions of viral RNA cap (GpppA -> m(7)GpppA -> m(7)GpppAm). The order of two methylations is determined by the preference of 2'-O methylation for substrate m(7)GpppA-RNA to GpppA-RNA, and the 2'-O methylation is not absolutely dependent on the prior N-7 methylation. A mutation that completely abolished the 2'-O methylation attenuated DENV replication in cell culture, whereas another mutation that abolished both methylations was lethal for viral replication, suggesting that N-7 methylation is more important than 2'-O methylation in viral replication. The latter mutant with lethal replication could be rescued by trans complementation using a wild-type DENV replicon. Furthermore, we found that chimeric DENVs containing the West Nile virus methyltransferase, polymerase, or full-length NS5 were nonreplicative, but the replication defect could also be rescued through trans complementation using the wild-type DENV replicon. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:568 / 578
页数:11
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