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pubmed-article:9566887pubmed:abstractTextInitiation of simian virus 40 (SV40) DNA replication is dependent upon the assembly of two T-antigen (T-ag) hexamers on the SV40 core origin. To further define the oligomerization mechanism, the pentanucleotide requirements for T-ag assembly were investigated. Here, we demonstrate that individual pentanucleotides support hexamer formation, while particular pairs of pentanucleotides suffice for the assembly of T-ag double hexamers. Related studies demonstrate that T-ag double hexamers formed on "active pairs" of pentanucleotides catalyze a set of previously described structural distortions within the core origin. For the four-pentanucleotide-containing wild-type SV40 core origin, footprinting experiments indicate that T-ag double hexamers prefer to bind to pentanucleotides 1 and 3. Collectively, these experiments demonstrate that only two of the four pentanucleotides in the core origin are necessary for T-ag assembly and the induction of structural changes in the core origin. Since all four pentanucleotides in the wild-type origin are necessary for extensive DNA unwinding, we concluded that the second pair of pentanucleotides is required at a step subsequent to the initial assembly process.lld:pubmed
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pubmed-article:9566887pubmed:authorpubmed-author:LawK AKAlld:pubmed
pubmed-article:9566887pubmed:authorpubmed-author:BullockP APAlld:pubmed
pubmed-article:9566887pubmed:authorpubmed-author:JooW SWSlld:pubmed
pubmed-article:9566887pubmed:authorpubmed-author:SreekumarK...lld:pubmed
pubmed-article:9566887pubmed:authorpubmed-author:PurvianceJ...lld:pubmed
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pubmed-article:9566887pubmed:volume18lld:pubmed
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