| pubmed-article:8676478 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:8676478 | lifeskim:mentions | umls-concept:C0206679 | lld:lifeskim |
| pubmed-article:8676478 | lifeskim:mentions | umls-concept:C0012863 | lld:lifeskim |
| pubmed-article:8676478 | lifeskim:mentions | umls-concept:C0021467 | lld:lifeskim |
| pubmed-article:8676478 | lifeskim:mentions | umls-concept:C0598312 | lld:lifeskim |
| pubmed-article:8676478 | lifeskim:mentions | umls-concept:C0021469 | lld:lifeskim |
| pubmed-article:8676478 | lifeskim:mentions | umls-concept:C0123145 | lld:lifeskim |
| pubmed-article:8676478 | lifeskim:mentions | umls-concept:C1292733 | lld:lifeskim |
| pubmed-article:8676478 | pubmed:issue | 7 | lld:pubmed |
| pubmed-article:8676478 | pubmed:dateCreated | 1996-8-15 | lld:pubmed |
| pubmed-article:8676478 | pubmed:abstractText | Cellular topoisomerase II is specifically inactivated by the drug ICRF-193. This compound turns topoisomerase II into a closed clamp that is unable to cleave DNA. We have investigated the effects of this inhibitor on the replication of herpes simplex virus type 1. We show that ICRF-193 at low multiplicities of infection dramatically inhibits viral DNA synthesis and the production of infectious virus. The inhibition is less efficient at high multiplicities of infection. In addition, inhibition of viral DNA synthesis was observed only when ICRF-193 was present during the first 4 h of the infectious cycle. The transient replication of plasmids containing a herpes simplex virus type 1 origin of DNA replication, oriS, was affected by ICRF-193 in the same way. In contrast, neither cellular DNA synthesis nor replication of plasmids containing a simian virus 40 origin of DNA replication was inhibited. The observed effect on herpes simplex virus DNA replication was not caused by a decreased transcription of replication genes inasmuch as the levels of UL8, UL9, UL29, and UL30 rmRNAs were unaffected by the drug. These results suggest that topoisomerase II plays a vital role during the replication of herpes simplex virus type 1 DNA. We speculate that topoisomerase II is involved in the decatenation of newly synthesized daughter molecules. | lld:pubmed |
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| pubmed-article:8676478 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:8676478 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:8676478 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:8676478 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:8676478 | pubmed:issn | 0022-538X | lld:pubmed |
| pubmed-article:8676478 | pubmed:author | pubmed-author:EliasPP | lld:pubmed |
| pubmed-article:8676478 | pubmed:author | pubmed-author:YanYY | lld:pubmed |
| pubmed-article:8676478 | pubmed:author | pubmed-author:HammarstenOO | lld:pubmed |
| pubmed-article:8676478 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:8676478 | pubmed:volume | 70 | lld:pubmed |
| pubmed-article:8676478 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:8676478 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:8676478 | pubmed:pagination | 4523-9 | lld:pubmed |
| pubmed-article:8676478 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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