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单纯疱疹病毒DNA的剖析。VI. 缺陷DNA源自S成分。

Anatomy of herpes simplex virus DNA. VI. Defective DNA originates from the S component.

作者信息

Frenkeĺ N, Locker H, Batterson W, Hayward G S, Roizman B

出版信息

J Virol. 1976 Nov;20(2):527-31. doi: 10.1128/JVI.20.2.527-531.1976.

DOI:10.1128/JVI.20.2.527-531.1976
PMID:185428
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC355020/
Abstract

We previously reported that serial propagation of the Justin strain of herpes simplex virus 1 [HSV-1 (Justin)] results in the generation of defective DNA molecules consisting of tandem repetitions of sequences of limited complexity. In the present study, HSV-1 DNA was cleaved with the restriction endonucleases BglII and EcoRI. The fragments were electrophoretically separated on agarose gels, transferred to nitrocellulose strips, and then hybridized with 32P-labeled HSV-1 (Justin) defective DNA. The data allow us to conclude that DNA sequences contained in the repeat unit of defective DNA originate from the S segment of the wild-type viral DNA molecule.

摘要

我们之前报道过,单纯疱疹病毒1型(HSV-1)贾斯汀株(HSV-1 (Justin))的连续传代导致产生了由有限复杂性序列的串联重复组成的缺陷性DNA分子。在本研究中,HSV-1 DNA用限制性内切酶BglII和EcoRI进行切割。片段在琼脂糖凝胶上进行电泳分离,转移到硝酸纤维素条上,然后与32P标记的HSV-1 (Justin)缺陷性DNA杂交。这些数据使我们能够得出结论,缺陷性DNA重复单元中包含的DNA序列源自野生型病毒DNA分子的S片段。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/835e/355020/1d48b97abc37/jvirol00227-0187-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/835e/355020/dab6dfae7fdc/jvirol00227-0186-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/835e/355020/1d48b97abc37/jvirol00227-0187-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/835e/355020/dab6dfae7fdc/jvirol00227-0186-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/835e/355020/1d48b97abc37/jvirol00227-0187-a.jpg

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本文引用的文献

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Regulation of herpesvirus macromolecular synthesis. I. Cascade regulation of the synthesis of three groups of viral proteins.疱疹病毒大分子合成的调控。I. 三组病毒蛋白合成的级联调控。
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The U(L)15 gene of herpes simplex virus type 1 contains within its second exon a novel open reading frame that is translated in frame with the U(L)15 gene product.单纯疱疹病毒1型的U(L)15基因在其第二个外显子内包含一个新的开放阅读框,该阅读框与U(L)15基因产物读码框一致进行翻译。
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PCR detection of amplified 132 bp repeats in Marek's disease virus type 1 (MDV-1) DNA can serve as an indicator for critical genomic rearrangement leading to the attenuation of virus virulence.1型马立克氏病病毒(MDV-1)DNA中132bp重复序列的PCR检测可作为关键基因组重排的指标,这种重排会导致病毒毒力减弱。
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Cloning and characterization of herpes simplex virus type 1 oriL: comparison of replication and protein-DNA complex formation by oriL and oriS.单纯疱疹病毒1型oriL的克隆与特性分析:oriL与oriS的复制及蛋白质-DNA复合物形成的比较
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