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在感染猿猴病毒40的细胞中复制的传染性线性DNA序列。

Infectious linear DNA sequences replicating in simian virus 40-infected cells.

作者信息

Gruss P, Sauer G

出版信息

J Virol. 1977 Feb;21(2):565-78. doi: 10.1128/JVI.21.2.565-578.1977.

DOI:10.1128/JVI.21.2.565-578.1977
PMID:189087
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC353859/
Abstract

A new class of linear duplex DNA structures that contain simian virus 40 (SV40) DNA sequences and that are replicated during productive infection of cells with SV40 is described. These structures comprise up to 35% of the radioactively labeled DNA molecules that can be isolated by selective extraction. These molecules represent a unique size class corresponding to the length of an open SV40 DNA molecule (FO III), and they contain a heterogeneous population of DNA sequences either of host or of viral origin, as shown by restriction endonuclease analysis and nucleic acid hybridization. Part of the FO III DNA molecules contain viral-host DNA sequences covalently linked with each other. They start to replicate with the onset of SV40 superhelix replication 1 day after infection. Their rate of synthesis is most pronounced 3 days after infection when superhelix replication is already declining. Furthermore, they cannot be chased into other structures. At least a fraction of these molecules is infectious when administered together with DEAE-dextran to permissive cells. After intracellular circularization, superhelical DNA FO I with an aberrant cleavage pattern accumulates. In addition, tumor and viral capsid antigen are induced, and infectious viral progeny is obtained. Infection of cells with purified SV40 FO I DNA does not result in FO III DNA molecules in the infected cells or in the viral progeny. It is suggested, therefore, that these FO III DNA molecules are perpetuated within SV40 virus pools by encapsidation into pseudovirions.

摘要

描述了一类新的线性双链DNA结构,其包含猿猴病毒40(SV40)DNA序列,并且在细胞被SV40有效感染期间进行复制。这些结构占可通过选择性提取分离的放射性标记DNA分子的35%。这些分子代表了一个独特的大小类别,对应于开放的SV40 DNA分子(FO III)的长度,并且如限制性内切酶分析和核酸杂交所示,它们包含宿主或病毒来源的异质DNA序列群体。部分FO III DNA分子包含彼此共价连接的病毒-宿主DNA序列。它们在感染后1天随着SV40超螺旋复制的开始而开始复制。它们的合成速率在感染后3天最为明显,此时超螺旋复制已经下降。此外,它们不能被追踪到其他结构中。当与DEAE-葡聚糖一起施用于允许性细胞时,这些分子中至少一部分具有感染性。细胞内环化后,具有异常切割模式的超螺旋DNA FO I会积累。此外,会诱导肿瘤和病毒衣壳抗原,并获得感染性病毒后代。用纯化的SV40 FO I DNA感染细胞不会在感染细胞或病毒后代中产生FO III DNA分子。因此,有人提出,这些FO III DNA分子通过被包装到假病毒颗粒中而在SV40病毒库中得以延续。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e51e/353859/b8faf5557c6b/jvirol00206-0147-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e51e/353859/0dd0c20fa66a/jvirol00206-0138-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e51e/353859/434bdb62cc0f/jvirol00206-0140-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e51e/353859/b8faf5557c6b/jvirol00206-0147-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e51e/353859/0dd0c20fa66a/jvirol00206-0138-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e51e/353859/434bdb62cc0f/jvirol00206-0140-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e51e/353859/b8faf5557c6b/jvirol00206-0147-a.jpg

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