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人巨细胞病毒AD169株的末端结构与异质性

Terminal structure and heterogeneity in human cytomegalovirus strain AD169.

作者信息

Tamashiro J C, Spector D H

出版信息

J Virol. 1986 Sep;59(3):591-604. doi: 10.1128/JVI.59.3.591-604.1986.

DOI:10.1128/JVI.59.3.591-604.1986
PMID:3016322
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC253215/
Abstract

We have characterized the heterogeneity occurring at the junction of the long (L) and short (S) segments and at the termini of the strain AD169 human cytomegalovirus (HCMV) genome by restriction endonuclease mapping and nucleotide sequence analyses. The HCMV a sequence was identified by its position at both termini and inverted orientation at the L-S junction. Heterogeneity at both termini and the L-S junction was generated by the presence of fused and tandem a sequences. Some S termini lacked an a sequence. In addition, near the L terminus and at the L-S junction there were a variable number of 217-base-pair (bp) XhoI fragments arranged in tandem. The 217-bp fragments consisted of a portion of the a and adjacent b sequences (in the L-segment repeat) bounded by the same direct repeats (DR1) found at the boundaries of the a sequence. A model for the generation of these heterogeneous fragments is presented. We also determined the sequence of seven cloned terminal fragments, five from the L terminus and two from the S terminus. All L termini contained identical terminal sequences ending with base 32 of a 33-bp DR1. The S termini differed from each other and from the L-segment termini. One S terminus lacked an a sequence and terminated within S-segment repeat (c) sequences. The second S terminus contained an a sequence and terminated with bases 20 to 33 of a 33-bp DR1. A comparison of the cloned L and S terminal sequences with cloned L-S junction sequences suggested that the termini contained 3' single base extensions which were removed during the cloning. We also show that the herpesvirus conserved sequence is in a similar position relative to the termini of HCMV and several other herpesviruses, thus adding further support for the role of the sequence in the maturation of viral DNA.

摘要

我们通过限制性内切酶图谱分析和核苷酸序列分析,对人巨细胞病毒(HCMV)AD169株基因组的长(L)、短(S)片段连接处及末端的异质性进行了表征。HCMV a序列通过其在两个末端的位置以及在L-S连接处的反向排列得以鉴定。两个末端和L-S连接处的异质性是由融合和串联的a序列的存在所产生的。一些S末端缺少a序列。此外,在L末端附近和L-S连接处有可变数量的217碱基对(bp)XhoI片段串联排列。217-bp片段由a序列的一部分和相邻的b序列(在L片段重复序列中)组成,其边界由在a序列边界发现的相同直接重复序列(DR1)界定。本文提出了这些异质片段产生的模型。我们还测定了七个克隆末端片段的序列,五个来自L末端,两个来自S末端。所有L末端都含有相同的末端序列,以33-bp DR1的第32个碱基结尾。S末端彼此不同,也与L片段末端不同。一个S末端缺少a序列,并在S片段重复(c)序列内终止。第二个S末端含有a序列,并以33-bp DR1的第20至33个碱基结尾。将克隆的L和S末端序列与克隆的L-S连接序列进行比较表明,末端含有3'单碱基延伸,在克隆过程中被去除。我们还表明,疱疹病毒保守序列相对于HCMV和其他几种疱疹病毒的末端处于相似位置,从而进一步支持了该序列在病毒DNA成熟中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f44/253215/68b2316113c0/jvirol00108-0075-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f44/253215/3db39bf43aa5/jvirol00108-0070-a.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f44/253215/68b2316113c0/jvirol00108-0075-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f44/253215/3db39bf43aa5/jvirol00108-0070-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f44/253215/ae773df7d6e0/jvirol00108-0072-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f44/253215/5df2eb2dd0fa/jvirol00108-0073-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f44/253215/804757308feb/jvirol00108-0074-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f44/253215/68b2316113c0/jvirol00108-0075-a.jpg

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