首页> 美国卫生研究院文献>Journal of Virology >Human herpesvirus 6B origin: sequence diversity requirement for two binding sites for origin-binding protein and enhanced replication from origin multimers.
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Human herpesvirus 6B origin: sequence diversity requirement for two binding sites for origin-binding protein and enhanced replication from origin multimers.

机译:人类疱疹病毒6B起源:序列多样性起源结合蛋白需要两个结合位点以及来自起源多聚体的复制增强。

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摘要

A previously identified human herpesvirus 6B (HHV-6B) origin of DNA replication contains two binding sites for the origin-binding protein (OBPH6B). We have investigated the functional significance of these sites by determining the replication efficiencies of mutated origin sequences, using a transient replication assay. The results indicate that both sites are required for DNA replication. In addition, we have tested the functional consequences of linear sequence amplifications in the origin. The data show that tandemized origin elements are more efficiently replicated than single-copy origins. Finally, we have determined the extent of interstrain origin sequence variation that exists among HHV-6 isolates by cloning, sequencing, and analyzing origins from a number of virus isolates, including examples of both HHV-6A and HHV-6B.
机译:DNA复制的先前鉴定的人类疱疹病毒6B(HHV-6B)起点包含起点结合蛋白(OBPH6B)的两个结合位点。我们已经通过使用瞬时复制测定法确定突变来源序列的复制效率来研究了这些位点的功能意义。结果表明两个位点都是DNA复制所必需的。另外,我们已经测试了起源中线性序列扩增的功能后果。数据显示,与单拷贝原点相比,串联原点元素的复制效率更高。最后,我们通过克隆,测序和分析来自许多病毒分离株的起源(包括HHV-6A和HHV-6B的实例),确定了HHV-6分离株之间存在的株间起源序列差异的程度。

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