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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1984-3-2
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pubmed:abstractText |
The transposase of bacteriophage Mu (gene A protein) mediates the coupled replication and integration processes that constitute transposition during the lytic cycle. Our previous results showed that the activity of the A protein is unstable, as its continued synthesis is required to maintain Mu DNA replication throughout the lytic cycle. We present here the results of experiments in which the A protein is used stoichiometrically and must be synthesized de novo for each round of Mu DNA replication. Induction of a Mu lysogen in the absence of DNA replication allows accumulation of potential for a single round of Mu DNA replication. Once achieved, this potential is stable even in the absence of further protein synthesis. Release of inhibition of DNA replication leads to a single semi-conservative replicative transposition event, followed by later rounds only if additional synthesis of the A protein is allowed.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Jan
|
pubmed:issn |
0092-8674
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
36
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
197-202
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:6319007-Bacteriophage mu,
pubmed-meshheading:6319007-DNA Replication,
pubmed-meshheading:6319007-Lysogeny,
pubmed-meshheading:6319007-Nucleotidyltransferases,
pubmed-meshheading:6319007-Transposases,
pubmed-meshheading:6319007-Viral Proteins,
pubmed-meshheading:6319007-Virus Activation,
pubmed-meshheading:6319007-Virus Replication
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pubmed:year |
1984
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pubmed:articleTitle |
Stoichiometric use of the transposase of bacteriophage Mu.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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