Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
1995-4-10
pubmed:abstractText
The DNA of human parvovirus adeno-associated virus type 2 (AAV) integrates preferentially into a defined region of human chromosome 19. Southern blots of genomic DNA from latently infected cell lines revealed that the provirus was not simply inserted into the cellular DNA. Both the proviral and adjoining cellular DNA organization indicated that integration occurred by a complex, coordinated process involving limited DNA replication and rearrangements. However, the mechanism for targeted integration has remained obscure. The two larger nonstructural proteins (Rep68 and Rep78) of AAV bind to a sequence element that is present in both the integration locus (P1) and the AAV inverted terminal repeat. This binding may be important for targeted integration. To investigate the mechanism of targeted integration, we tested the cloned integration site subfragment in a cell-free replication assay in the presence or absence of recombinant Rep proteins. Extensive, asymmetric replication of linear or open-circular template DNA was dependent on the presence of P1 sequence and Rep protein. The activities of Rep on the cloned P1 element are analogous to activities on the AAV inverted terminal repeat. Replication apparently initiates from a 3'-OH generated by the sequence-specific nicking activity of Rep. This results in a covalent attachment between Rep and the 5'-thymidine of the nick. The complexity of proviral structures can be explained by the participation of limited DNA replication facilitated by Rep during integration.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-1064029, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-1316261, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-1316616, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-1334463, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-1336449, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-1369403, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-1651588, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-1653762, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-1657596, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-1671045, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-1671046, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-1850104, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-1850805, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-202398, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-2156265, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-2156820, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-2159383, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-2215424, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-2542617, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-2549858, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-2562399, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-2840659, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-2894681, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-2993858, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-3018548, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-3023870, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-3041032, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-6281769, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-6298451, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-6319005, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-6329712, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-6352411, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-7910375, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-7933128, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-8016070, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-8032195, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-8032196, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-8057478, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-8223465, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-8289342, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-8289383, http://linkedlifedata.com/resource/pubmed/commentcorrection/7884849-8380475
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0022-538X
pubmed:author
pubmed:issnType
Print
pubmed:volume
69
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2038-46
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1995
pubmed:articleTitle
Asymmetric replication in vitro from a human sequence element is dependent on adeno-associated virus Rep protein.
pubmed:affiliation
Molecular Hematology Branch, National Heart, Lung, and Blood Institute, Bethesda, Maryland 20892.
pubmed:publicationType
Journal Article
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