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Analysis of the termini of the DNA of bovine parvovirus: demonstration of sequence inversion at the left terminus and its implication for the replication model.

作者信息

Chen K C, Shull B C, Lederman M, Stout E R, Bates R C

机构信息

Department of Biology, Virginia Polytechnic Institute and State University, Blacksburg 24061.

出版信息

J Virol. 1988 Oct;62(10):3807-13. doi: 10.1128/JVI.62.10.3807-3813.1988.

DOI:10.1128/JVI.62.10.3807-3813.1988
PMID:2843676
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC253526/
Abstract

The distribution of terminal-sequence orientations in the viral DNA of bovine parvovirus (BPV), an autonomous parvovirus, was studied by end labeling and restriction enzyme digestion and also by cloning. The left (3') end of the minus strand of BPV was found in two alternative sequence orientations (designated as flip and flop, which are reverse complements of each other), with a 10-fold excess of flip. This is in contrast to the autonomous rodent parvoviruses which encapsidate minus-strand DNA with only the flip orientation at this end. The right (5') end of the minus strand of BPV contained both sequence orientations with equal frequencies, as in the rodent parvoviruses. Sequence inversions were also detected at both ends of the plus strand, which makes up about 10% of the encapsidated BPV DNA. Each terminus of BPV DNA had a characteristic ratio of flip to flop forms, and this ratio was restored in the progeny DNA resulting from transfection with genomic clones of different defined terminal conformations. Replicative-form DNA showed the same distribution of terminal-sequence orientations as the reannealed plus and minus virion DNAs, suggesting that the distribution of flip and flop forms observed in virion DNA is not due to selective encapsidation, but rather to the specific distribution of replicative forms. The current replication model for autonomous parvoviruses, which was based on the available data for the rodent parvoviruses, cannot account for the observed distribution of BPV DNA. An alternative model is suggested.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab16/253526/ee7915565b65/jvirol00089-0280-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab16/253526/6992d22f4b27/jvirol00089-0278-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab16/253526/ada4d3b959cb/jvirol00089-0279-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab16/253526/ee7915565b65/jvirol00089-0280-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab16/253526/6992d22f4b27/jvirol00089-0278-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab16/253526/ada4d3b959cb/jvirol00089-0279-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab16/253526/ee7915565b65/jvirol00089-0280-a.jpg

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本文引用的文献

1
Maturation of parvovirus LuIII in a subcellular system. I. Optimal conditions for in vitro synthesis and encapsidation of viral DNA.细小病毒LuIII在亚细胞系统中的成熟。I. 病毒DNA体外合成与衣壳化的最佳条件。
J Gen Virol. 1983 May;64(Pt 5):1043-54. doi: 10.1099/0022-1317-64-5-1043.
2
Autonomous parvovirus LuIII encapsidates equal amounts of plus and minus DNA strands.自主细小病毒LuIII包裹等量的正链和负链DNA。
J Virol. 1984 Feb;49(2):319-24. doi: 10.1128/JVI.49.2.319-324.1984.
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Buffer gradient gels and 35S label as an aid to rapid DNA sequence determination.
Cold Spring Harb Perspect Biol. 2013 Feb 1;5(2):a012989. doi: 10.1101/cshperspect.a012989.
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Detection of head-to-tail DNA sequences of human bocavirus in clinical samples.检测临床样本中人博卡病毒的头对头 DNA 序列。
PLoS One. 2011 May 4;6(5):e19457. doi: 10.1371/journal.pone.0019457.
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Identification and molecular cloning of a novel porcine parvovirus.鉴定和分子克隆一种新型猪细小病毒。
Arch Virol. 2010 May;155(5):801-6. doi: 10.1007/s00705-010-0646-8. Epub 2010 Mar 26.
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Molecular characterization of infectious clones of the minute virus of canines reveals unique features of bocaviruses.犬微小病毒感染性克隆的分子特征揭示了博卡病毒的独特特性。
J Virol. 2009 Apr;83(8):3956-67. doi: 10.1128/JVI.02569-08. Epub 2009 Feb 11.
7
The transcription profile of the bocavirus bovine parvovirus is unlike those of previously characterized parvoviruses.博卡病毒牛细小病毒的转录谱不同于先前已鉴定的细小病毒。
J Virol. 2007 Nov;81(21):12080-5. doi: 10.1128/JVI.00815-07. Epub 2007 Aug 22.
8
Symmetric-strand packaging of recombinant parvovirus LuIII genomes that retain only the terminal regions.仅保留末端区域的重组细小病毒LuIII基因组的对称链包装。
J Virol. 1995 Apr;69(4):2692-6. doi: 10.1128/JVI.69.4.2692-2696.1995.
9
The mismatched nucleotides in the 5'-terminal hairpin of minute virus of mice are required for efficient viral DNA replication.小鼠微小病毒5'末端发夹结构中的错配核苷酸是高效病毒DNA复制所必需的。
J Virol. 1995 Dec;69(12):7489-96. doi: 10.1128/JVI.69.12.7489-7496.1995.
10
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J Virol. 1989 Jul;63(7):3180-4. doi: 10.1128/JVI.63.7.3180-3184.1989.
缓冲液梯度凝胶和35S标记辅助快速DNA序列测定。
Proc Natl Acad Sci U S A. 1983 Jul;80(13):3963-5. doi: 10.1073/pnas.80.13.3963.
4
Aphidicolin inhibition of the production of replicative-form DNA during bovine parvovirus infection.阿非科林对牛细小病毒感染期间复制型DNA产生的抑制作用。
J Virol. 1984 Mar;49(3):652-7. doi: 10.1128/JVI.49.3.652-657.1984.
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Nucleic Acids Res. 1983 Feb 25;11(4):999-1018. doi: 10.1093/nar/11.4.999.
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DNA sequence of the 5' terminus containing the replication origin of parvovirus replicative form DNA.包含细小病毒复制型DNA复制起点的5'末端的DNA序列。
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Cloning of adeno-associated virus into pBR322: rescue of intact virus from the recombinant plasmid in human cells.将腺相关病毒克隆至pBR322:在人细胞中从重组质粒拯救完整病毒。
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Terminal transferase-catalyzed addition of nucleotides to the 3' termini of DNA.末端转移酶催化的核苷酸添加到DNA的3'末端。
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9
Nucleotide sequence of the inverted terminal repetition in adeno-associated virus DNA.腺相关病毒DNA中反向末端重复序列的核苷酸序列。
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Characterization and molecular cloning of a human parvovirus genome.人类细小病毒基因组的特征分析与分子克隆
Science. 1984 Dec 7;226(4679):1161-5. doi: 10.1126/science.6095448.