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腺病毒DNA复制的起源:体内最小DNA序列要求

The origin of adenovirus DNA replication: minimal DNA sequence requirement in vivo.

作者信息

Hay R T

出版信息

EMBO J. 1985 Feb;4(2):421-6. doi: 10.1002/j.1460-2075.1985.tb03645.x.

DOI:10.1002/j.1460-2075.1985.tb03645.x
PMID:4018031
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC554202/
Abstract

Adenovirus mini-chromosomes which contain two cloned, inverted adenovirus termini replicate in vivo when supplied with non-defective adenovirus as a helper. This system has been used to define the minimum cis acting DNA sequences required for adenovirus DNA replication in vivo. Deletions into each end of the adenovirus inverted terminal repeat (ITR) were generated with Bal31 exonuclease and the resulting molecules constructed into plasmids which contained two inverted copies of the deleted ITR separated by the bacterial neomycin phosphotransferase gene. To determine the effect of the deletion in vivo plasmids cleaved to expose the adenovirus termini were co-transfected with adenovirus type 2 DNA into tissue culture cells. The replicative ability of the molecules bearing adenovirus termini was assayed by Southern blotting of extracted DNA which had been treated with DpnI, a restriction enzyme which cleaves only methylated and therefore unreplicated, input DNA. Molecules containing the terminal 45 bp of the viral genome were fully active whereas molecules containing only 36 bp were in-active in this assay. Therefore sequences required for DNA replication are contained entirely within the terminal 45 bp of the viral genome. Thus, both the previously described highly conserved region (nucleotides 9-18) and the binding site for the cellular nuclear factor I (nucleotides 19-48) are essential for adenovirus DNA replication in vivo.

摘要

当提供无缺陷腺病毒作为辅助病毒时,含有两个克隆的反向腺病毒末端的腺病毒微型染色体可在体内复制。该系统已被用于确定腺病毒DNA在体内复制所需的最小顺式作用DNA序列。用Bal31核酸外切酶对腺病毒反向末端重复序列(ITR)的两端进行缺失,并将所得分子构建到质粒中,该质粒包含由细菌新霉素磷酸转移酶基因隔开的两个缺失ITR的反向拷贝。为了确定缺失在体内的影响,将切割以暴露腺病毒末端的质粒与2型腺病毒DNA共转染到组织培养细胞中。通过对经DpnI处理的提取DNA进行Southern印迹分析来检测带有腺病毒末端的分子的复制能力,DpnI是一种仅切割甲基化且因此未复制的输入DNA的限制性酶。含有病毒基因组末端45bp的分子在该试验中具有完全活性,而仅含有36bp的分子则无活性。因此,DNA复制所需的序列完全包含在病毒基因组的末端45bp内。因此,先前描述的高度保守区域(核苷酸9 - 18)和细胞核因子I的结合位点(核苷酸19 - 48)对于腺病毒DNA在体内的复制都是必不可少的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21e3/554202/cde116c09856/emboj00267-0146-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21e3/554202/a6c23ab4348f/emboj00267-0146-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21e3/554202/cde116c09856/emboj00267-0146-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21e3/554202/a6c23ab4348f/emboj00267-0146-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21e3/554202/cde116c09856/emboj00267-0146-b.jpg

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Specific binding of the adenovirus terminal protein precursor-DNA polymerase complex to the origin of DNA replication.腺病毒末端蛋白前体 - DNA 聚合酶复合物与 DNA 复制起点的特异性结合。
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