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pubmed-article:8648649pubmed:abstractTextUsing 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.lld:pubmed
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pubmed-article:8648649pubmed:dateRevised2007-11-15lld:pubmed
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pubmed-article:8648649pubmed:articleTitleThe simian virus 40 packaging signal ses is composed of redundant DNA elements which are partly interchangeable.lld:pubmed
pubmed-article:8648649pubmed:affiliationDepartment of Hematology, Hebrew University Hadassah Medical School, Jerusalem, Israel.lld:pubmed
pubmed-article:8648649pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8648649pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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