Source:http://linkedlifedata.com/resource/pubmed/id/18635963
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
14
|
pubmed:dateCreated |
2008-7-25
|
pubmed:abstractText |
Progression through the mammalian cell division cycle is regulated by the sequential activation of cyclin-dependent kinases, CDKs, at specific phases of the cell cycle. Cyclin A-CDK2 and cyclin A-CDK1 phosphorylate nuclear substrates during S and G(2) phases, respectfully. However, the DNA helicase complex, MCM2-7, is loaded onto the origin of replications in G(1), prior to the normally scheduled induction of cyclin A. It has previously been shown that cyclin A-CDKs phosphorylate MCM2 and MCM4 in vitro, thereby diminishing helicase activity. Thus, in this study we hypothesize that, in vivo, cyclin A-CDK activity during G(1) would result in an inhibition of progression into the S phase. To test this, we establish an in vivo method of inducing cyclin A-CDK activity in G(1) phase and observe that activation of cyclin A-CDK, but not cyclin E-CDK complexes, inhibit DNA synthesis without affecting other G(1) events such as cyclin D synthesis, E2F activation and cdc6 loading onto chromatin. We further report that the mechanism of this S phase inhibition occurs, at least in part, through impaired loading of MCM onto chromatin, presumably due to decreased levels of cdt1 and premature phosphorylation of MCM by cyclin A-CDK. In addition to providing in vivo confirmation of in vitro predictions regarding cyclin A-CDK phosphorylation of the MCM complex, our results provide insight into the cellular effects of unscheduled cyclin A-CDK activity in mammalian cells.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Chromatin,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclin A,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclin-Dependent Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/DNA,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Localization Signals
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jul
|
pubmed:issn |
1551-4005
|
pubmed:author | |
pubmed:issnType |
Electronic
|
pubmed:day |
15
|
pubmed:volume |
7
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
2179-88
|
pubmed:dateRevised |
2009-11-19
|
pubmed:meshHeading |
pubmed-meshheading:18635963-Animals,
pubmed-meshheading:18635963-CHO Cells,
pubmed-meshheading:18635963-Chromatin,
pubmed-meshheading:18635963-Cricetinae,
pubmed-meshheading:18635963-Cricetulus,
pubmed-meshheading:18635963-Cyclin A,
pubmed-meshheading:18635963-Cyclin-Dependent Kinases,
pubmed-meshheading:18635963-DNA,
pubmed-meshheading:18635963-DNA-Binding Proteins,
pubmed-meshheading:18635963-G1 Phase,
pubmed-meshheading:18635963-Humans,
pubmed-meshheading:18635963-Nuclear Localization Signals,
pubmed-meshheading:18635963-Protein Transport,
pubmed-meshheading:18635963-S Phase
|
pubmed:year |
2008
|
pubmed:articleTitle |
Cyclin A-CDK activity during G1 phase impairs MCM chromatin loading and inhibits DNA synthesis in mammalian cells.
|
pubmed:affiliation |
Department of Pharmacological Sciences at Saint Louis University, St. Louis, Missouri 63104, USA.
|
pubmed:publicationType |
Journal Article
|