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猿猴病毒40包装信号序列由部分可互换的冗余DNA元件组成。

The simian virus 40 packaging signal ses is composed of redundant DNA elements which are partly interchangeable.

作者信息

Dalyot-Herman N, Ben-nun-Shaul O, Gordon-Shaag A, Oppenheim A

机构信息

Department of Hematology, Hebrew University Hadassah Medical School, Jerusalem, Israel.

出版信息

J Mol Biol. 1996 May 31;259(1):69-80. doi: 10.1006/jmbi.1996.0302.

Abstract

Using the experimental system of simian virus 40 (SV40) pseudovirions we have previously shown that SV40 requires a specific DNA element for packaging, ses, which was mapped to the SV40 regulatory region. ses was previously found to play a role in facilitating the nucleosomal rearrangement required for chromatin condensation and viral packaging. Here, the fine structure of ses was investigated by genetic studies. Analyses of ses+ revertants indicated that in order to function, ses must be present in close proximity to the origin of replication (ori), supporting a role in the regulation of the viral life cycle. Fine dissection of ses was performed using a series of plasmids carrying mutations and deletions in this region. The results suggest that multiple DNA elements participate in the SV40 packaging process, including the GC-boxes and elements derived from the enhancer. The elements are redundant, and they can function in various combinations. Packaging efficiency correlated with the number of GC-boxes, known to bind Sp1. In addition, AP-2 binding elements appeared to more important than others. These findings were supported by experiments which showed that packaging was significantly enhanced by adding AP-2 binding sites to plasmids with large deletions and lacking those sites. The results imply that binding of Sp1 and/or AP-2 may participate in the packaging process.

摘要

利用猿猴病毒40(SV40)假病毒的实验系统,我们先前已表明SV40包装需要一个特定的DNA元件,即ses,它被定位到SV40调控区。先前发现ses在促进染色质浓缩和病毒包装所需的核小体重排中发挥作用。在此,通过遗传学研究对ses的精细结构进行了探究。对ses +回复突变体的分析表明,为了发挥功能,ses必须紧邻复制起点(ori)存在,这支持了其在病毒生命周期调控中的作用。使用一系列携带该区域突变和缺失的质粒对ses进行了精细剖析。结果表明,多个DNA元件参与SV40包装过程,包括GC盒和源自增强子的元件。这些元件是冗余的,并且它们可以以各种组合发挥作用。包装效率与已知可结合Sp1的GC盒数量相关。此外,AP - 2结合元件似乎比其他元件更重要。这些发现得到了实验的支持,实验表明,通过向具有大缺失且缺乏这些位点的质粒中添加AP - 2结合位点,包装显著增强。结果表明Sp1和/或AP - 2的结合可能参与包装过程。

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