AIDS Research Group, IDIBAPS, E-08036 Barcelona, Spain.
Virus Res. 2013 Feb;171(2):287-303. doi: 10.1016/j.virusres.2012.09.008. Epub 2012 Sep 24.
HIV-1 reverse transcription is achieved in the newly infected cell before viral DNA (vDNA) nuclear import. Reverse transcriptase (RT) has previously been shown to function as a molecular motor, dismantling the nucleocapsid complex that binds the viral genome as soon as plus-strand DNA synthesis initiates. We first propose a detailed model of this dismantling in close relationship with the sequential conversion from RNA to double-stranded (ds) DNA, focusing on the nucleocapsid protein (NCp7). The HIV-1 DNA-containing pre-integration complex (PIC) resulting from completion of reverse transcription is translocated through the nuclear pore. The PIC nucleoprotein architecture is poorly understood but contains at least two HIV-1 proteins initially from the virion core, namely integrase (IN) and the viral protein r (Vpr). We next present a set of electron micrographs supporting that Vpr behaves as a DNA architectural protein, initiating multiple DNA bridges over more than 500 base pairs (bp). These complexes are shown to interact with NCp7 bound to single-stranded nucleic acid regions that are thought to maintain IN binding during dsDNA synthesis, concurrently with nucleocapsid complex dismantling. This unexpected binding of Vpr conveniently leads to a compacted but filamentous folding of the vDNA that should favor its nuclear import. Finally, nucleocapsid-like aggregates engaged in dsDNA synthesis appear to efficiently bind to F-actin filaments, a property that may be involved in targeting complexes to the nuclear envelope. More generally, this article highlights unique possibilities offered by in vitro reconstitution approaches combined with macromolecular imaging to gain insights into the mechanisms that alter the nucleoprotein architecture of the HIV-1 genome, ultimately enabling its insertion into the nuclear chromatin.
HIV-1 的逆转录是在新感染的细胞中进行的,在此之前病毒 DNA(vDNA)尚未进入细胞核。先前的研究表明,逆转录酶(RT)可以作为一种分子马达,一旦启动正链 DNA 合成,就会将结合病毒基因组的核衣壳复合物解体。我们首次提出了一个详细的模型,该模型与从 RNA 到双链 DNA 的顺序转换密切相关,重点是核衣壳蛋白(NCp7)。逆转录完成后形成的含有 HIV-1 DNA 的整合前复合物(PIC)通过核孔转运。PIC 的核蛋白结构尚不清楚,但至少包含两种最初来自病毒核心的 HIV-1 蛋白,即整合酶(IN)和病毒蛋白 r(Vpr)。接下来,我们展示了一组电子显微镜照片,支持 Vpr 作为一种 DNA 结构蛋白的行为,它可以在超过 500 个碱基对(bp)的区域上引发多个 DNA 桥。这些复合物被证明与结合单链核酸区域的 NCp7 相互作用,这些区域被认为在 dsDNA 合成过程中保持 IN 的结合,同时进行核衣壳复合物的解体。Vpr 的这种意外结合方便地导致了 vDNA 的压缩但丝状折叠,这应该有利于其核导入。最后,参与 dsDNA 合成的核衣壳样聚集体似乎有效地与 F-肌动蛋白丝结合,这一特性可能参与将复合物靶向核膜。更一般地说,本文强调了体外重建方法与大分子成像相结合提供的独特可能性,以深入了解改变 HIV-1 基因组核蛋白结构的机制,最终使其能够插入核染色质。