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Boundaries and structure of human cytomegalovirus oriLyt a complex origin for lytic-phase DNA replication.

机译:人巨细胞病毒oriLyt的边界和结构裂解相DNA复制的复杂来源。

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摘要

We have localized a cis-acting sequence that promotes initiation of lytic-phase DNA replication (oriLyt) within the HindIII D fragment of the human cytomegalovirus (HCMV) AD169 genome and investigated its sequence requirements by testing the ability of plasmid constructs to mediate DNA replication in a transient transfection-plus-infection assay. Replication of plasmids containing HCMV oriLyt required at least the virus-specified DNA polymerase activity supplied by HCMV infection of transfected cells and was autonomous in that it did not result from recombination with the virus genome. Progeny molecules in the transient assay were high-molecular-weight tandem oligomers, which is consistent with predictions of a rolling-circle model. Experiments testing subclones of HindIII-D defined a core 2.4-kbp region containing elements required for oriLyt function that extended rightward from around 1.0 kbp upstream of UL57 near the middle of the long unique component of the virus genome. Sequences flanking this core also were needed for full activity. The defined region contains at least four clustered sets of repeated sequence elements identical to or candidate counterparts of elements present in the corresponding cytomegalovirus Colburn lytic-phase replication origin. These elements are novel in that they apparently do not correspond to previously characterized motifs. Also present are multiple copies of elements similar to known binding sites for the transcription factors ATF/CREB, MLTF/USF, and Sp1. Preliminary deletion analysis suggests that multiple components within the boundaries of oriLyt cooperate to enable initiation of HCMV lytic-phase DNA synthesis.
机译:我们已经定位了一个顺式作用序列,该序列可促进人类巨细胞病毒(HCMV)AD169基因组HindIII D片段内的裂解相DNA复制(oriLyt)的启动,并通过测试质粒构建体介导DNA复制的能力来研究其序列需求在瞬时转染加感染测定中。包含HCMV oriLyt的质粒的复制至少需要由转染细胞的HCMV感染提供的病毒指定的DNA聚合酶活性,并且具有自主性,因为它不是与病毒基因组重组产生的。瞬时分析中的子代分子是高分子量串联寡聚物,与滚环模型的预测相符。测试HindIII-D亚克隆的实验定义了一个2.4kbp的核心区域,该区域包含oriLyt功能所需的元件,该元件从UL57上游约1.0kbp处向右延伸,靠近病毒基因组的长唯一成分的中间。完整活动也需要位于该核心两侧的序列。限定的区域包含至少四个重复序列元件的聚类组,这些重复序列元件与相应的巨细胞病毒科尔本裂解相复制起点中存在的元件相同或候选的对应物。这些元素是新颖的,因为它们显然不对应于先前表征的图案。还存在类似于转录因子ATF / CREB,MLTF / USF和Sp1的已知结合位点的元件的多个拷贝。初步的缺失分析表明,oriLyt边界内的多个组分协同作用,从而能够启动HCMV裂解相DNA合成。

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