Suppr超能文献

具有可反转L组分的伪狂犬病病毒变异体中重组连接点处的核苷酸序列。

Nucleotide sequences at recombinational junctions present in pseudorabies virus variants with an invertible L component.

作者信息

Lu Z Q, DeMarchi J M, Harper L, Rall G F, Ben-Porat T

机构信息

Department of Microbiology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232.

出版信息

J Virol. 1989 Jun;63(6):2690-8. doi: 10.1128/JVI.63.6.2690-2698.1989.

Abstract

The genome of pseudorabies virus (PrV) consists of two components--a noninvertible long (L) and an invertible short (S) component. The S component is bracketed by inverted repeats. In some variant strains of PrV (which have a selective growth advantage in certain cell lines), a sequence normally present at the left end of the L component has been translocated to the right end of the L component next to the inverted repeat. Consequently, these strains have acquired a genome with an L component that is bracketed by inverted repeats and that also inverts. We have determined the restriction maps and have analyzed the nucleotide sequences of those parts of the genome of three strains with invertible L components that contain the translocated segment of DNA. The results were as follows. The translocated fragments were derived in all cases from the extreme left end of the L component only. The sizes of the translocated fragments were similar, ranging from 1.3 to 1.4 kilobase pairs. The junction between the L and S components in these strains was the same as that in standard viral concatemeric DNA. The translocation of sequences from the left end of the genome next to the inverted repeats was always accompanied by a deletion of sequences from the right end of the L component. The sizes of the deleted fragments varied considerably, ranging from 0.8 to 2.3 kilobase pairs. Sequence homology at the points of recombination, i.e., at the junction between the right end and the left end of the L component, existed sometimes but not always. A model depicting how a virus with a class 2 genome (such as PrV) may acquire a genome with characteristics of a class 3 genome (such as herpes simplex virus) is presented.

摘要

伪狂犬病病毒(PrV)的基因组由两个部分组成——一个不可反转的长(L)组分和一个可反转的短(S)组分。S组分由反向重复序列包围。在PrV的一些变异株中(这些变异株在某些细胞系中具有选择性生长优势),通常位于L组分左端的一个序列已易位至L组分右端紧邻反向重复序列的位置。因此,这些毒株获得了一个基因组,其L组分被反向重复序列包围且也会发生反转。我们已经确定了三种具有可反转L组分且包含DNA易位片段的毒株基因组部分的限制性图谱,并分析了其核苷酸序列。结果如下。所有情况下,易位片段均仅源自L组分的最左端。易位片段的大小相似,范围为1.3至1.4千碱基对。这些毒株中L和S组分之间的连接与标准病毒串联DNA中的连接相同。基因组左端紧邻反向重复序列处的序列易位总是伴随着L组分右端序列的缺失。缺失片段的大小差异很大,范围为0.8至2.3千碱基对。重组位点处,即L组分右端和左端之间的连接处,有时存在序列同源性,但并非总是如此。本文提出了一个模型,描述具有2类基因组的病毒(如PrV)如何获得具有3类基因组特征的基因组(如单纯疱疹病毒)。

相似文献

3
Functions of the sequences at the ends of the inverted repeats of pseudorabies virus.
J Virol. 1992 Mar;66(3):1506-19. doi: 10.1128/JVI.66.3.1506-1519.1992.
6
Structural organization of the termini of the L and S components of the genome of pseudorabies virus.
J Virol. 1990 Oct;64(10):4968-77. doi: 10.1128/JVI.64.10.4968-4977.1990.
8
Low-level inversion of the L component of pseudorabies virus is not dependent on sequence homology.
J Virol. 1991 Dec;65(12):7016-9. doi: 10.1128/JVI.65.12.7016-7019.1991.
10
Fine mapping of the immediate-early gene of the Indiana-Funkhauser strain of pseudorabies virus.
J Virol. 1988 Dec;62(12):4763-6. doi: 10.1128/JVI.62.12.4763-4766.1988.

引用本文的文献

2
New nucleotide sequence data on the EMBL File Server.
Nucleic Acids Res. 1989 Sep 25;17(18):7553-78. doi: 10.1093/nar/17.18.7553.
3
Structural organization of the termini of the L and S components of the genome of pseudorabies virus.
J Virol. 1990 Oct;64(10):4968-77. doi: 10.1128/JVI.64.10.4968-4977.1990.
6
Analysis of an origin of DNA replication located at the L terminus of the genome of pseudorabies virus.
J Virol. 1991 Nov;65(11):6283-91. doi: 10.1128/JVI.65.11.6283-6291.1991.
8
Functions of the sequences at the ends of the inverted repeats of pseudorabies virus.
J Virol. 1992 Mar;66(3):1506-19. doi: 10.1128/JVI.66.3.1506-1519.1992.

本文引用的文献

1
Amino acid metabolism in mammalian cell cultures.
Science. 1959 Aug 21;130(3373):432-7. doi: 10.1126/science.130.3373.432.
4
Sequencing end-labeled DNA with base-specific chemical cleavages.
Methods Enzymol. 1980;65(1):499-560. doi: 10.1016/s0076-6879(80)65059-9.
8
cis Functions involved in replication and cleavage-encapsidation of pseudorabies virus.
J Virol. 1986 Aug;59(2):318-27. doi: 10.1128/JVI.59.2.318-327.1986.
10
Detection of specific sequences among DNA fragments separated by gel electrophoresis.
J Mol Biol. 1975 Nov 5;98(3):503-17. doi: 10.1016/s0022-2836(75)80083-0.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验