Romero Tammy A, Tumban Ebenezer, Jun Jeongwon, Lott William B, Hanley Kathryn A
Molecular Biology Program, New Mexico State University (NMSU), Las Cruces, NM 88003, USA.
School of Life Sciences, Queensland University of Technology, Brisbane, QLD 4001, Australia.
J Gen Virol. 2006 Nov;87(Pt 11):3291-3296. doi: 10.1099/vir.0.82182-0.
Several studies have generated computer-based predictions of secondary structure of the 3' untranslated region (UTR) of Dengue virus (DEN); however, experimental verification of the formation of these structures in vitro is lacking. This study assessed the congruence of Mfold predictions of secondary structure of the core region of the DEN type 4 3' UTR with nuclease maps of this region. Maps and predictions were largely consistent. Maps supported the existence of previously predicted pseudoknots and identified putative regions of dynamic folding. Additionally, this study investigated previously identified conserved elements in the flavivirus 3' UTR that differ among viruses with different modes of transmission. Specific regions of mosquito-borne DEN type 4 were either deleted or replaced with homologous sequences from tick-borne Langat virus. All of these mutations caused substantial distortion of secondary structure, yet viruses carrying these mutations were viable.
多项研究已生成基于计算机的登革病毒(DEN)3'非翻译区(UTR)二级结构预测;然而,缺乏对这些结构在体外形成的实验验证。本研究评估了登革4型3'UTR核心区域二级结构的Mfold预测与该区域核酸酶图谱的一致性。图谱和预测结果基本一致。图谱支持了先前预测的假结的存在,并确定了动态折叠的推定区域。此外,本研究调查了黄病毒3'UTR中先前确定的保守元件,这些元件在具有不同传播模式的病毒之间存在差异。蚊媒传播的登革4型的特定区域被删除或用蜱媒传播的兰加特病毒的同源序列取代。所有这些突变都导致二级结构严重扭曲,但携带这些突变的病毒仍具有活性。