Fleming Aaron M, Ding Yun, Alenko Anton, Burrows Cynthia J
Department of Chemistry, University of Utah , 315 South 1400 East, Salt Lake City, Utah 84112-0850, United States.
ACS Infect Dis. 2016 Oct 14;2(10):674-681. doi: 10.1021/acsinfecdis.6b00109. Epub 2016 Aug 12.
Zika virus has emerged as a global concern because neither a vaccine nor antiviral compounds targeting it exist. A structure for the positive-sense RNA genome has not been established, leading us to look for potential G-quadruplex sequences (PQS) in the genome. The analysis identified >60 PQSs in the Zika genome. To minimize the PQS population, conserved sequences in the Flaviviridae family were found by sequence alignment, identifying seven PQSs in the prM, E, NS1, NS3, and NS5 genes. Next, alignment of 78 Zika strain genomes identified a unique PQS near the end of the 3'-UTR. Structural studies on the G-quadruplex sequences found four of the conserved Zika virus sequences to adopt stable, parallel-stranded folds that bind a G-quadruplex-specific compound, and one that was studied caused polymerase stalling when folded to a G-quadruplex. Targeting these PQSs with G-quadruplex binding molecules validated in previous clinical trials may represent a new approach for inhibiting viral replication.
寨卡病毒已成为全球关注的问题,因为针对它的疫苗和抗病毒化合物均不存在。目前尚未确定正链RNA基因组的结构,这促使我们在基因组中寻找潜在的G-四链体序列(PQS)。分析在寨卡病毒基因组中鉴定出60多个PQS。为了尽量减少PQS的数量,通过序列比对在黄病毒科中发现了保守序列,在prM、E、NS1、NS3和NS5基因中鉴定出7个PQS。接下来,对78个寨卡病毒株基因组进行比对,在3'-UTR末端附近发现了一个独特的PQS。对G-四链体序列的结构研究发现,寨卡病毒的四个保守序列形成了稳定的平行链折叠结构,可与一种G-四链体特异性化合物结合,并且其中一个序列折叠成G-四链体时会导致聚合酶停滞。用先前临床试验中验证的G-四链体结合分子靶向这些PQS可能代表了一种抑制病毒复制的新方法。