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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。

Analysis of an origin of DNA replication located at the L terminus of the genome of pseudorabies virus.

作者信息

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

机构信息

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

出版信息

J Virol. 1991 Nov;65(11):6283-91. doi: 10.1128/JVI.65.11.6283-6291.1991.

Abstract

We have localized an origin of DNA replication at the L terminus of the pseudorabies virus genome. This origin differs in location as well as in general structure from the origins of replication of other herpesviruses that have been identified. The 600 leftmost nucleotides of the genome that were found to include origin function have been analyzed. This sequence is composed of an 82-bp palindrome whose center of symmetry is separated by 352 unique bp (UL2). Within the UL2, a sequence that fits the consensus sequence of the NF1 binding site, as well as one that has partial homology to the binding site of UL9 of herpes simplex virus, is present. Using truncated fragments of DNA, sequences essential for minimal origin function were delimited to within a fragment that includes the terminal 104 bp of the left end of the genome. Within these 104 bp, two elements essential to origin function have been identified. One of these elements is present within the terminal 64 bp of the L component (within one of the palindromic arms). The other is present within the 22 bp of the UL2 adjacent to this palindromic arm. Other auxiliary elements, although not essential for origin function, contribute to more efficient replication. The NF1 and UL9 binding site homologies were found to be nonessential to origin function.

摘要

我们已将伪狂犬病病毒基因组DNA复制起点定位在L末端。该起点在位置以及总体结构上与已鉴定的其他疱疹病毒的复制起点不同。已对基因组最左边的600个核苷酸进行了分析,发现其包含复制起点功能。该序列由一个82bp的回文序列组成,其对称中心被352个独特的bp(UL2)隔开。在UL2内,存在一个符合NF1结合位点共有序列的序列,以及一个与单纯疱疹病毒UL9结合位点具有部分同源性的序列。使用DNA截短片段,将最小复制起点功能所必需的序列限定在一个包含基因组左端末端104bp的片段内。在这104bp内,已鉴定出两个对复制起点功能至关重要的元件。其中一个元件存在于L组分的末端64bp内(在其中一个回文臂内)。另一个存在于与该回文臂相邻的UL2的22bp内。其他辅助元件虽然对复制起点功能不是必需的,但有助于更高效地复制。发现NF1和UL9结合位点的同源性对复制起点功能并非必需。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd21/250332/271310ad18b8/jvirol00054-0643-a.jpg

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