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在感染3型腺病毒的HeLa细胞中合成缺陷型病毒DNA。

Synthesis of defective viral DNA in HeLa cells infected with adenovirus type 3.

作者信息

Daniell E, Mullenbach T

出版信息

J Virol. 1978 Apr;26(1):61-70. doi: 10.1128/JVI.26.1.61-70.1978.

DOI:10.1128/JVI.26.1.61-70.1978
PMID:650739
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC354034/
Abstract

Virus-specific DNA fragments that are shorter than the full-length viral genomes have been isolated from HeLa cells productively infected with adenovirus type 3. A number of predominant size classes could be detected by gel electrophoresis and hybridization, and the array of sizes was similar or identical to the selection in DNA purified from incomplete particles of this serotype (E. Daniell, J. Virol. 19:685-708, 1976). A large fraction of these short DNA molecules contained long inverted terminal repetitions, as did DNA molecules from incomplete particles. Restriction analysis showed that these subgenomic molecules consist of sequences from the two molecular ends of the normal genome. These results suggest that the predominance of left-hand end fragments seen in packaged incomplete DNAs results from selective packaging, whereas the predominance of certain size classes of intracellular viral DNA is a function of prepackaging events. The incomplete DNAs were generated at all times during viral DNA replication, and the yield relative to complete DNA did not seem to vary significantly with time or multiplicity of infection or when the virus was propagated on different human cell types.

摘要

从被3型腺病毒有效感染的HeLa细胞中分离出了比全长病毒基因组短的病毒特异性DNA片段。通过凝胶电泳和杂交可检测到许多主要的大小类别,其大小阵列与从该血清型不完整颗粒中纯化的DNA中的选择相似或相同(E. Daniell,《病毒学杂志》19:685 - 708,1976)。这些短DNA分子中的很大一部分含有长的反向末端重复序列,不完整颗粒中的DNA分子也是如此。限制性分析表明,这些亚基因组分子由正常基因组两个分子末端的序列组成。这些结果表明,在包装的不完整DNA中看到的左手末端片段的优势是由选择性包装导致的,而细胞内病毒DNA某些大小类别的优势是预包装事件的一个函数。不完整DNA在病毒DNA复制的所有时间都产生,相对于完整DNA的产量似乎不会随时间、感染复数或病毒在不同人类细胞类型上繁殖而显著变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a197/354034/d466c901663a/jvirol00196-0079-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a197/354034/7fe13bc2dcf1/jvirol00196-0073-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a197/354034/491c53a43e51/jvirol00196-0074-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a197/354034/93725044baa6/jvirol00196-0075-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a197/354034/b22ecdd50c06/jvirol00196-0075-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a197/354034/d466c901663a/jvirol00196-0079-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a197/354034/7fe13bc2dcf1/jvirol00196-0073-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a197/354034/491c53a43e51/jvirol00196-0074-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a197/354034/93725044baa6/jvirol00196-0075-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a197/354034/b22ecdd50c06/jvirol00196-0075-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a197/354034/d466c901663a/jvirol00196-0079-a.jpg

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本文引用的文献

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Subgenomic viral DNA species synthesized in simian cells by human and simian adenoviruses.人和猴腺病毒在猴细胞中合成的亚基因组病毒DNA种类。
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Structural organization and polypeptide composition of the avian adenovirus core.禽腺病毒核心的结构组织和多肽组成
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