首页> 美国卫生研究院文献>Journal of Virology >Sequences within the Herpesvirus-Conserved pac1 and pac2 Motifs Are Required for Cleavage and Packaging of the Murine Cytomegalovirus Genome
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Sequences within the Herpesvirus-Conserved pac1 and pac2 Motifs Are Required for Cleavage and Packaging of the Murine Cytomegalovirus Genome

机译:裂解和包装小鼠巨细胞病毒基因组需要疱疹病毒保守的pac1和pac2母题中的序列。

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摘要

The DNA sequence motifs pac1 [an A-rich region flanked by poly(C) runs] and pac2 (CGCGGCG near an A-rich region) are conserved near herpesvirus genomic termini and are believed to mediate cleavage of genomes from replicative concatemers. To determine their importance in the cleavage process, we constructed a number of recombinant murine cytomegaloviruses with a second cleavage site inserted at an ectopic location within the viral genome. Cleavage at a wild-type ectopic site occurred as frequently as at the natural cleavage site, whereas mutation of this ectopic site revealed that some of the conserved motifs of pac1 and pac2 were essential for cleavage whereas others were not. Within pac1, the left poly(C) region was very important for cleavage and packaging but the A-rich region was not. Within pac2, the A-rich region and adjacent sequences were essential for cleavage and packaging and the CGCGGCG region contributed to, but was not strictly essential for, efficient cleavage and packaging. A second A-rich region was not important at all. Furthermore, mutations that prevented cleavage also blocked duplication and deletion of the murine cytomegalovirus 30-bp terminal repeat at the ectopic site, suggesting that repeat duplication and deletion are consequences of cleavage. Given that the processes of genome cleavage and packaging appear to be highly conserved among herpesviruses, these findings should be relevant to other members of this family.
机译:疱疹病毒基因组末端附近保守了DNA序列基序pac1 [位于A富集区域的poly(C)序列]和pac2(CGCGGCG位于A富集区域附近),并被认为介导了复制性连接体的基因组切割。为了确定它们在切割过程中的重要性,我们构建了许多重组鼠巨细胞病毒,并在病毒基因组内的异位插入了第二个切割位点。在野生型异位位点的裂解与在自然裂解位点发生的频率相同,而该异位位点的突变表明,pac1和pac2的某些保守基序对于裂解是必不可少的,而其他则不是。在pac1中,左侧的poly(C)区对于切割和包装非常重要,而富含A的区则不重要。在pac2中,富含A的区域和相邻序列对于切割和包装至关重要,而CGCGGCG区域对有效的切割和包装有所贡献,但并非严格如此。第二个富裕地区根本不重要。此外,阻止切割的突变也阻止了小鼠巨细胞病毒30 bp末端重复在异位点的重复和缺失,这表明重复重复和缺失是切割的结果。鉴于疱疹病毒之间基因组切割和包装的过程似乎是高度保守的,因此这些发现应与该家族的其他成员有关。

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