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野生型和中心DNA瓣缺陷型HIV-1慢病毒载体基因组:超微结构分辨率水平下的细胞内可视化

Wild-type and central DNA flap defective HIV-1 lentiviral vector genomes: intracellular visualization at ultrastructural resolution levels.

作者信息

Arhel Nathalie J, Souquere-Besse Sylvie, Charneau Pierre

机构信息

Groupe de Virologie Moléculaire et Vectorologie, Institut Pasteur, 25-28 rue du Dr, Roux, 75724 Paris, France.

出版信息

Retrovirology. 2006 Jun 26;3:38. doi: 10.1186/1742-4690-3-38.

Abstract

HIV-1 and other lentiviruses have the unique ability among retroviruses to efficiently replicate in non-dividing cells as a result of the active nuclear import of their DNA genome across an interphasic nuclear membrane. Previous work has shown that a three-stranded DNA structure synthesized during HIV-1 reverse transcription, called the central DNA flap, acts as a cis-determinant of HIV-1 genome nuclear import. Concordantly, DNA Flap re-insertion in lentiviral-derived gene therapy vectors stimulates gene transfer efficiencies and complements the level of nuclear import to wild-type levels quantitatively indistinguishable from wild-type virus in all cell types and tissues examined so far. In order to define the precise nature of the replicative defect of DNA flap mutant viruses, we carried out in situ DNA hybridization experiments with electron microscopy to determine the subcellular localization of DNA flap mutant and wild-type HIV-1 genomes. We found that Flap defective DNA genomes accumulate at the cytoplasmic face of the nuclear membrane with no overlap across the nuclear membrane, whereas wild-type genomes localize throughout the nuclear compartment. These data provide an unequivocal confirmation of the role of the DNA flap in HIV-1 nuclear import and further establish that the DNA flap controls a step that immediately precedes translocation through the nuclear pore. Further, the widespread distribution of wild-type genomes within the open chromatin confirms the recent genome-wide mapping of HIV-1 cDNA integration sites and points to an as-yet poorly understood step of intranuclear transport of HIV-1 pre-integration complexes.

摘要

HIV-1和其他慢病毒在逆转录病毒中具有独特能力,能够在非分裂细胞中高效复制,这是由于其DNA基因组通过间期核膜进行主动核输入的结果。先前的研究表明,HIV-1逆转录过程中合成的一种三链DNA结构,称为中央DNA瓣,作为HIV-1基因组核输入的顺式决定因素。相应地,在慢病毒衍生的基因治疗载体中重新插入DNA瓣可提高基因转移效率,并在所有已检测的细胞类型和组织中,将核输入水平补充到与野生型病毒在数量上难以区分的野生型水平。为了确定DNA瓣突变病毒复制缺陷的确切性质,我们进行了电子显微镜原位DNA杂交实验,以确定DNA瓣突变体和野生型HIV-1基因组的亚细胞定位。我们发现,有瓣缺陷的DNA基因组聚集在核膜的细胞质面,没有穿过核膜的重叠,而野生型基因组则分布在整个核区室。这些数据明确证实了DNA瓣在HIV-1核输入中的作用,并进一步确定DNA瓣控制着一个紧接通过核孔转运之前的步骤。此外,野生型基因组在开放染色质中的广泛分布证实了最近对HIV-1 cDNA整合位点的全基因组图谱分析,并指出了HIV-1预整合复合物核内运输中一个尚未充分理解的步骤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a178/1538615/4f60483ac85e/1742-4690-3-38-1.jpg

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