Department of Viral Infections, RIMD, Osaka Univ. 3-1 Yamadaoka, Suita, Osaka 565-0871, Japan.
Nucleic Acids Res. 2012 Jun;40(11):5012-22. doi: 10.1093/nar/gks156. Epub 2012 Feb 10.
The dimer initiation site/dimer linkage sequence (DIS/DLS) region of the human immunodeficiency virus type 1 (HIV-1) RNA genome is suggested to play essential roles at various stages of the viral life cycle. Through a novel assay we had recently developed, we reported on the necessary and sufficient region for RNA dimerization in the HIV-1 virion. Using this system, we performed further detailed mapping of the functional base pairs necessary for HIV-1 DLS structure. Interestingly, the study revealed a previously unnoticed stem formation between two distantly positioned regions. Based on this and other findings on functional base pairing in vivo, we propose new 3D models of the HIV-1 DLS which contain a unique pseudoknot-like conformation. Since this pseudoknot-like conformation appears to be thermodynamically stable, forms a foundational skeleton for the DLS and sterically restricts the spontaneous diversification of DLS conformations, its unique shape may contribute to the viral life cycle and potentially serve as a novel target for anti-HIV-1 therapies.
人免疫缺陷病毒 1 型(HIV-1)RNA 基因组的二聚体起始位点/二聚体连接序列(DIS/DLS)区域被认为在病毒生命周期的各个阶段发挥重要作用。通过我们最近开发的一种新测定法,我们报告了 HIV-1 病毒粒子中 RNA 二聚化所必需的和充分的区域。使用该系统,我们进一步详细绘制了 HIV-1 DLS 结构所必需的功能碱基对的图谱。有趣的是,该研究揭示了两个相隔较远的区域之间以前未被注意到的茎形成。基于这一点以及体内功能碱基配对的其他发现,我们提出了 HIV-1 DLS 的新 3D 模型,其中包含独特的拟似发夹状构象。由于这种拟似发夹状构象似乎在热力学上是稳定的,形成了 DLS 的基础骨架,并在空间上限制了 DLS 构象的自发多样化,因此其独特的形状可能有助于病毒生命周期,并可能成为抗 HIV-1 治疗的新靶标。