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本文引用的文献

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Expression and maturation of human foamy virus Gag precursor polypeptides.人泡沫病毒Gag前体多肽的表达与成熟
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Reverse transcription. Foamy viruses bubble on.逆转录。泡沫病毒继续存在。
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In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector.慢病毒载体介导的非分裂细胞的体内基因递送与稳定转导
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Human foamy virus replication: a pathway distinct from that of retroviruses and hepadnaviruses.人泡沫病毒复制:一条不同于逆转录病毒和嗜肝DNA病毒的途径。
Science. 1996 Mar 15;271(5255):1579-82. doi: 10.1126/science.271.5255.1579.
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Intracellular transport of the murine leukemia virus during acute infection of NIH 3T3 cells: nuclear import of nucleocapsid protein and integrase.小鼠白血病病毒在NIH 3T3细胞急性感染期间的细胞内运输:核衣壳蛋白和整合酶的核输入
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Foamy virus vectors.泡沫病毒载体
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Human foamy virus polypeptides: identification of env and bel gene products.人泡沫病毒多肽:env和bel基因产物的鉴定
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Transient immunosuppressive effect induced in rabbits and mice by the human spumaretrovirus prototype HFV (human foamy virus).
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9
Passage through mitosis is required for oncoretroviruses but not for the human immunodeficiency virus.致肿瘤逆转录病毒需要经历有丝分裂,而人类免疫缺陷病毒则不需要。
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A defective human foamy provirus generated by pregenome splicing.由前基因组剪接产生的有缺陷的人类泡沫病毒前病毒。
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进入的人泡沫病毒Gag蛋白的核靶向涉及一个中心粒步骤。

Nuclear targeting of incoming human foamy virus Gag proteins involves a centriolar step.

作者信息

Saïb A, Puvion-Dutilleul F, Schmid M, Périès J, de Thé H

机构信息

CNRS UPR 9051, Hôpital Saint-Louis, Paris, France.

出版信息

J Virol. 1997 Feb;71(2):1155-61. doi: 10.1128/JVI.71.2.1155-1161.1997.

DOI:10.1128/JVI.71.2.1155-1161.1997
PMID:8995637
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC191168/
Abstract

The pathways used in the transport of retroviral genomes to the nucleus are poorly identified. Analyzing the intracellular localization of incoming foamy viruses, we have found that the Gag antigens and the viral genome accumulate in a distinct perinuclear domain identified as the centrosome. Colchicine treatment completely abolished pericentriolar targeting of human foamy virus (HFV) proteins, suggesting a role for microtubules in the transport of the incoming viral proteins to the centrioles. Finally, we demonstrate that, similarly to human immunodeficiency virus DNA, HFV DNA can enter the nucleus of G1/S-phase-arrested cells, although no viral gene expression can be observed. Recent observations have demonstrated that foamy viruses have several features not shared by other retroviruses. The intracellular route of the incoming Gag antigens may constitute a new specificity of this class of viruses.

摘要

逆转录病毒基因组向细胞核运输所使用的途径目前还不太明确。通过分析传入的泡沫病毒在细胞内的定位,我们发现Gag抗原和病毒基因组聚集在一个被确定为中心体的独特核周区域。秋水仙碱处理完全消除了人类泡沫病毒(HFV)蛋白向中心粒周围的靶向定位,这表明微管在将传入的病毒蛋白运输到中心粒过程中发挥了作用。最后,我们证明,与人类免疫缺陷病毒DNA类似,HFV DNA可以进入G1/S期阻滞细胞的细胞核,尽管未观察到病毒基因表达。最近的观察结果表明,泡沫病毒具有其他逆转录病毒所没有的几个特征。传入的Gag抗原的细胞内途径可能构成了这类病毒的一种新特性。