Source:http://linkedlifedata.com/resource/pubmed/id/21450947
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
Pt 7
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pubmed:dateCreated |
2011-6-20
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pubmed:abstractText |
Cyclin-dependent protein kinases (CDKs) are important regulators of cellular processes and are functionally integrated into the replication of human cytomegalovirus (HCMV). Recently, a regulatory impact of CDK activity on the viral mRNA export factor pUL69 was shown. Here, specific aspects of the mode of interaction between CDK9/cyclin T1 and pUL69 are described. Intracellular localization was studied in the presence of a novel selective CDK9 inhibitor, R22, which exerts anti-cytomegaloviral activity in vitro. A pronounced R22-induced formation of nuclear speckled aggregation of pUL69 was demonstrated. Multi-labelling confocal laser-scanning microscopy revealed that CDK9 and cyclin T1 co-localized perfectly with pUL69 in individual speckles. The effects were similar to those described recently for the broad CDK inhibitor roscovitine. Co-immunoprecipitation and yeast two-hybrid analyses showed that cyclin T1 interacted with both CDK9 and pUL69. The interaction region of pUL69 for cyclin T1 could be attributed to aa 269-487. Moreover, another component of CDK inhibitor-induced speckled aggregates was identified with RNA polymerase II, supporting earlier reports that strongly suggested an association of pUL69 with transcription complexes. Interestingly, when using a UL69-deleted recombinant HCMV, no speckled aggregates were formed by CDK inhibitor treatment. This indicated that pUL69 is the defining component of aggregates and generally may represent a crucial viral interactor of cyclin T1. In conclusion, these data emphasize that HCMV inter-regulation with CDK9/cyclin T1 is at least partly based on a pUL69-cylin T1 interaction, thus contributing to the importance of CDK9 for HCMV replication.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/CCNT1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclin T,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclin-Dependent Kinase 9,
http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators,
http://linkedlifedata.com/resource/pubmed/chemical/pUL69 protein, Human herpesvirus 5
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
1465-2099
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
92
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1519-31
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pubmed:meshHeading |
pubmed-meshheading:21450947-Cell Line,
pubmed-meshheading:21450947-Cell Nucleus,
pubmed-meshheading:21450947-Cyclin T,
pubmed-meshheading:21450947-Cyclin-Dependent Kinase 9,
pubmed-meshheading:21450947-Cytomegalovirus,
pubmed-meshheading:21450947-Cytomegalovirus Infections,
pubmed-meshheading:21450947-Humans,
pubmed-meshheading:21450947-Protein Binding,
pubmed-meshheading:21450947-Protein Transport,
pubmed-meshheading:21450947-Trans-Activators,
pubmed-meshheading:21450947-Virus Replication
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pubmed:year |
2011
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pubmed:articleTitle |
Recruitment of cyclin-dependent kinase 9 to nuclear compartments during cytomegalovirus late replication: importance of an interaction between viral pUL69 and cyclin T1.
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pubmed:affiliation |
Institute for Clinical and Molecular Virology, University of Erlangen-Nuremberg, Erlangen, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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