| pubmed-article:216004 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:216004 | lifeskim:mentions | umls-concept:C0319132 | lld:lifeskim |
| pubmed-article:216004 | lifeskim:mentions | umls-concept:C0008546 | lld:lifeskim |
| pubmed-article:216004 | lifeskim:mentions | umls-concept:C0014230 | lld:lifeskim |
| pubmed-article:216004 | lifeskim:mentions | umls-concept:C0598312 | lld:lifeskim |
| pubmed-article:216004 | lifeskim:mentions | umls-concept:C0439659 | lld:lifeskim |
| pubmed-article:216004 | lifeskim:mentions | umls-concept:C0205227 | lld:lifeskim |
| pubmed-article:216004 | pubmed:issue | 12 | lld:pubmed |
| pubmed-article:216004 | pubmed:dateCreated | 1979-3-13 | lld:pubmed |
| pubmed-article:216004 | pubmed:abstractText | Isolated simian virus 40 (SV40) and polyoma nucleoprotein complexes contain endonuclease that, under in vitro conditions, converts part (up to 30%) of the covalently closed superhelical DNA to full-length linear rods. The positions of the cleavage sites within the genomes of SV40 and polyoma were determined by digestion with various single-cut restriction endonucleases and subsequent agarose gel electrophoresis of the cleavage products. Both SV40 and polyoma covalently closed superhelical DNA were cleaved open at their respective origins of DNA replication (+/- 75 base pairs). The full-length linear DNA rods whose ends map adjacent to the origin of DNA replication could also be isolated by sodium dodecyl sulfate/phenol extraction both from SV40-infected permissive cells and from purified SV40 virions. These data reveal the presence of a unique structure of the papovavirus chromatin close to the initiation site of DNA replication. | lld:pubmed |
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| pubmed-article:216004 | pubmed:language | eng | lld:pubmed |
| pubmed-article:216004 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:216004 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:216004 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:216004 | pubmed:month | Dec | lld:pubmed |
| pubmed-article:216004 | pubmed:issn | 0027-8424 | lld:pubmed |
| pubmed-article:216004 | pubmed:author | pubmed-author:GrussPP | lld:pubmed |
| pubmed-article:216004 | pubmed:author | pubmed-author:SauerGG | lld:pubmed |
| pubmed-article:216004 | pubmed:author | pubmed-author:ChowdhuryKK | lld:pubmed |
| pubmed-article:216004 | pubmed:author | pubmed-author:WaldeckWW | lld:pubmed |
| pubmed-article:216004 | pubmed:author | pubmed-author:FöhringBB | lld:pubmed |
| pubmed-article:216004 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:216004 | pubmed:volume | 75 | lld:pubmed |
| pubmed-article:216004 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:216004 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:216004 | pubmed:pagination | 5964-8 | lld:pubmed |
| pubmed-article:216004 | pubmed:dateRevised | 2010-9-2 | lld:pubmed |
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| pubmed-article:216004 | pubmed:year | 1978 | lld:pubmed |
| pubmed-article:216004 | pubmed:articleTitle | Origin of DNA replication in papovavirus chromatin is recognized by endogenous endonuclease. | lld:pubmed |
| pubmed-article:216004 | pubmed:publicationType | Journal Article | lld:pubmed |
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