• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

伪狂犬病病毒基因组L和S组分末端的结构组织

Structural organization of the termini of the L and S components of the genome of pseudorabies virus.

作者信息

DeMarchi J M, Lu Z Q, Rall G, Kupershmidt S, Ben-Porat T

机构信息

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

出版信息

J Virol. 1990 Oct;64(10):4968-77. doi: 10.1128/JVI.64.10.4968-4977.1990.

DOI:10.1128/JVI.64.10.4968-4977.1990
PMID:2168980
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC247988/
Abstract

The sequences of several hundred nucleotides around the junctions between the L and S components in concatemeric DNA and in mature virion DNA were ascertained. The two ends of the mature genome (which are joined in concatemeric DNA) show no sequence homology. Several directly repeated elements are present near both ends of the genome. Furthermore, the last 82 nucleotides at the left end of the L component (and of the genome) are repeated in inverted form (inverted repeat within the L component [IRL]) approximately 350 to 600 nucleotides downstream (depending on the virus isolate) bracketing the UL2 component. A comparison between the sequences at the right and left ends of the L component of the genome showed patchy homology, probably representing a vestigial inverted repeat bracketing the L component (IRL). Furthermore, less than 5% of the genomes have an L component that is in the orientation opposite to that of most of the viral genomes, indicating that the vestigial IRL that brackets the UL sequence may be sufficient to mediate inversion of the L component in some of the genomes. On the other hand, the UL2 component, which is bracketed by a perfect IRL, does not invert to a greater extent than does the L component (if it inverts at all). Analysis of the nucleotide sequence at the concatemeric junction of three different pseudorabies virus isolates showed almost complete sequence conservation. The sequence and organization of the repeated elements in the different isolates were almost identical, despite their different histories and origins. The high degree of conservation of these repeated elements implies that they may fulfill an essential function in the life cycle of the virus.

摘要

确定了串联DNA和成熟病毒体DNA中L和S组分连接处周围数百个核苷酸的序列。成熟基因组的两端(在串联DNA中相连)没有序列同源性。在基因组两端附近存在几个直接重复元件。此外,L组分(以及基因组)左端的最后82个核苷酸以反向形式重复(L组分内的反向重复序列[IRL]),在下游约350至600个核苷酸处(取决于病毒分离株),包围着UL2组分。对基因组L组分左右两端序列的比较显示出斑驳的同源性,可能代表包围L组分的残余反向重复序列(IRL)。此外,不到5%的基因组其L组分的方向与大多数病毒基因组相反,这表明包围UL序列的残余IRL可能足以介导某些基因组中L组分的反向。另一方面,被完美IRL包围的UL2组分,其反向程度并不比L组分(如果它发生反向的话)更大。对三种不同伪狂犬病病毒分离株串联连接处核苷酸序列的分析显示出几乎完全的序列保守性。尽管不同分离株的历史和起源不同,但它们中重复元件的序列和组织几乎相同。这些重复元件的高度保守性意味着它们可能在病毒的生命周期中发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da7a/247988/9d5e8e50b986/jvirol00065-0382-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da7a/247988/9d5e8e50b986/jvirol00065-0382-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da7a/247988/9d5e8e50b986/jvirol00065-0382-a.jpg

相似文献

1
Structural organization of the termini of the L and S components of the genome of pseudorabies virus.伪狂犬病病毒基因组L和S组分末端的结构组织
J Virol. 1990 Oct;64(10):4968-77. doi: 10.1128/JVI.64.10.4968-4977.1990.
2
Low-level inversion of the L component of pseudorabies virus is not dependent on sequence homology.伪狂犬病病毒L组分的低水平反向不依赖于序列同源性。
J Virol. 1991 Dec;65(12):7016-9. doi: 10.1128/JVI.65.12.7016-7019.1991.
3
Nucleotide sequences at recombinational junctions present in pseudorabies virus variants with an invertible L component.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。
J Virol. 1989 Jun;63(6):2690-8. doi: 10.1128/JVI.63.6.2690-2698.1989.
4
Sequence of the genome ends and of the junction between the ends in concatemeric DNA of pseudorabies virus.伪狂犬病病毒多联体DNA中基因组末端及末端间连接区的序列
J Virol. 1986 Dec;60(3):1183-5. doi: 10.1128/JVI.60.3.1183-1185.1986.
5
Cleavage of concatemeric DNA at the internal junction of "translocation" mutants of pseudorabies virus and inversion of their L component appear to be linked.伪狂犬病病毒“易位”突变体内部连接处的串联DNA切割与其L成分的倒转似乎有关联。
Virology. 1992 Mar;187(1):223-32. doi: 10.1016/0042-6822(92)90310-l.
6
Functions of the sequences at the ends of the inverted repeats of pseudorabies virus.伪狂犬病病毒反向重复序列末端序列的功能。
J Virol. 1992 Mar;66(3):1506-19. doi: 10.1128/JVI.66.3.1506-1519.1992.
7
The ability of pseudorabies virus to grow in different hosts is affected by the duplication and translocation of sequences from the left end of the genome to the UL-US junction.伪狂犬病病毒在不同宿主中生长的能力受到基因组左端序列向UL-US连接区的重复和易位的影响。
J Virol. 1991 Nov;65(11):5839-47. doi: 10.1128/JVI.65.11.5839-5847.1991.
8
Evolution of pseudorabies virions containing genomes with an invertible long component after repeated passage in chicken embryo fibroblasts.在鸡胚成纤维细胞中反复传代后,含有具有可反转长组分基因组的伪狂犬病病毒粒子的演变。
J Virol. 1987 Jun;61(6):1772-80. doi: 10.1128/JVI.61.6.1772-1780.1987.
9
Analysis of an origin of DNA replication located at the L terminus of the genome of pseudorabies virus.对位于伪狂犬病病毒基因组L末端的一个DNA复制起点的分析。
J Virol. 1991 Nov;65(11):6283-91. doi: 10.1128/JVI.65.11.6283-6291.1991.
10
The structure of the pseudorabies virus genome at the end of the inverted repeat sequences proximal to the junction with the short unique region.在与短独特区域连接处近端的反向重复序列末端的伪狂犬病病毒基因组结构。
J Gen Virol. 1990 Oct;71 ( Pt 10):2433-41. doi: 10.1099/0022-1317-71-10-2433.

引用本文的文献

1
A wide extent of inter-strain diversity in virulent and vaccine strains of alphaherpesviruses.α疱疹病毒毒力株和疫苗株之间存在广泛的株间多样性。
PLoS Pathog. 2011 Oct;7(10):e1002282. doi: 10.1371/journal.ppat.1002282. Epub 2011 Oct 13.
2
Definition of the minimal cis-acting sequences necessary for genome maturation of the herpesvirus murine cytomegalovirus.疱疹病毒鼠巨细胞病毒基因组成熟所需最小顺式作用序列的定义。
J Virol. 2008 Mar;82(5):2394-404. doi: 10.1128/JVI.00063-07. Epub 2007 Dec 19.
3
The simian varicella virus genome contains an invertible 665 base pair terminal element that is absent in the varicella zoster virus genome.

本文引用的文献

1
Fragments from both termini of the herpes simplex virus type 1 genome contain signals required for the encapsidation of viral DNA.单纯疱疹病毒1型基因组两端的片段含有病毒DNA包装所需的信号。
Nucleic Acids Res. 1983 Dec 10;11(23):8205-20. doi: 10.1093/nar/11.23.8205.
2
Structure and role of the herpes simplex virus DNA termini in inversion, circularization and generation of virion DNA.单纯疱疹病毒DNA末端在病毒DNA倒置、环化及产生过程中的结构与作用
Cell. 1982 Nov;31(1):89-97. doi: 10.1016/0092-8674(82)90408-1.
3
Pathway of assembly of herpesvirus capsids: an analysis using DNA+ temperature-sensitive mutants of pseudorabies virus.
猿猴水痘病毒基因组包含一个665个碱基对的可倒置末端元件,而水痘带状疱疹病毒基因组中不存在该元件。
Virology. 2007 Sep 30;366(2):387-93. doi: 10.1016/j.virol.2007.04.030. Epub 2007 Jun 6.
4
The capsid-associated UL25 protein of the alphaherpesvirus pseudorabies virus is nonessential for cleavage and encapsidation of genomic DNA but is required for nuclear egress of capsids.甲型疱疹病毒伪狂犬病病毒的衣壳相关UL25蛋白对于基因组DNA的切割和包装并非必需,但对于衣壳的核输出是必需的。
J Virol. 2006 Jul;80(13):6235-46. doi: 10.1128/JVI.02662-05.
5
A 3' coterminal gene cluster in pseudorabies virus contains herpes simplex virus UL1, UL2, and UL3 gene homologs and a unique UL3.5 open reading frame.伪狂犬病病毒中的一个3' 共末端基因簇包含单纯疱疹病毒UL1、UL2和UL3基因同源物以及一个独特的UL3.5开放阅读框。
J Virol. 1993 Oct;67(10):5955-61. doi: 10.1128/JVI.67.10.5955-5961.1993.
6
Nucleotide sequence variations surrounding the standard recombination junction of pseudorabies viruses.伪狂犬病病毒标准重组连接周围的核苷酸序列变异
Nucleic Acids Res. 1993 Nov 25;21(23):5522-3. doi: 10.1093/nar/21.23.5522.
7
A deletion at the UL/IR junction reduces pseudorabies virus neurovirulence.UL/IR 交界处的缺失可降低伪狂犬病病毒的神经毒力。
J Virol. 1995 Feb;69(2):1334-8. doi: 10.1128/JVI.69.2.1334-1338.1995.
8
Low-level inversion of the L component of pseudorabies virus is not dependent on sequence homology.伪狂犬病病毒L组分的低水平反向不依赖于序列同源性。
J Virol. 1991 Dec;65(12):7016-9. doi: 10.1128/JVI.65.12.7016-7019.1991.
9
Acquisition of an additional internal cleavage site differentially affects the ability of pseudorabies virus to multiply in different host cells.额外内部切割位点的获得对伪狂犬病病毒在不同宿主细胞中增殖的能力有不同影响。
J Virol. 1991 Dec;65(12):6604-11. doi: 10.1128/JVI.65.12.6604-6611.1991.
10
Analysis of an origin of DNA replication located at the L terminus of the genome of pseudorabies virus.对位于伪狂犬病病毒基因组L末端的一个DNA复制起点的分析。
J Virol. 1991 Nov;65(11):6283-91. doi: 10.1128/JVI.65.11.6283-6291.1991.
疱疹病毒衣壳组装途径:使用伪狂犬病病毒DNA+温度敏感突变体的分析
Virology. 1982 Jan 30;116(2):544-61. doi: 10.1016/0042-6822(82)90147-7.
4
Replication of herpesvirus DNA.疱疹病毒DNA的复制。
Curr Top Microbiol Immunol. 1981;91:81-107. doi: 10.1007/978-3-642-68058-8_4.
5
Construction of a double-jointed herpes simplex viral DNA molecule: inverted repeats are required for segment inversion, and direct repeats promote deletions.双链单纯疱疹病毒DNA分子的构建:片段倒置需要反向重复序列,而正向重复序列促进缺失。
Virology. 1981 Aug;113(1):345-62. doi: 10.1016/0042-6822(81)90161-6.
6
Cloning in single-stranded bacteriophage as an aid to rapid DNA sequencing.利用单链噬菌体克隆辅助快速DNA测序。
J Mol Biol. 1980 Oct 25;143(2):161-78. doi: 10.1016/0022-2836(80)90196-5.
7
Molecular engineering of the herpes simplex virus genome: insertion of a second L-S junction into the genome causes additional genome inversions.单纯疱疹病毒基因组的分子工程:在基因组中插入第二个L-S连接会导致额外的基因组倒位。
Cell. 1980 Nov;22(1 Pt 1):243-55. doi: 10.1016/0092-8674(80)90172-5.
8
Sequencing end-labeled DNA with base-specific chemical cleavages.通过碱基特异性化学切割对末端标记的DNA进行测序。
Methods Enzymol. 1980;65(1):499-560. doi: 10.1016/s0076-6879(80)65059-9.
9
Replication of herpesvirus DNA. VI. Virions containing either isomer of pseudorabies virus DNA are infectious.疱疹病毒DNA的复制。VI. 含有伪狂犬病病毒DNA任一异构体的病毒粒子具有感染性。
Virology. 1980 Apr 30;102(2):370-80. doi: 10.1016/0042-6822(80)90104-x.
10
Structure of the genome termini of varicella-zoster virus.
J Gen Virol. 1984 Nov;65 ( Pt 11):1969-77. doi: 10.1099/0022-1317-65-11-1969.