| pubmed-article:9312049 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9312049 | lifeskim:mentions | umls-concept:C1003741 | lld:lifeskim |
| pubmed-article:9312049 | lifeskim:mentions | umls-concept:C1336789 | lld:lifeskim |
| pubmed-article:9312049 | lifeskim:mentions | umls-concept:C0040649 | lld:lifeskim |
| pubmed-article:9312049 | pubmed:issue | 19 | lld:pubmed |
| pubmed-article:9312049 | pubmed:dateCreated | 1997-12-10 | lld:pubmed |
| pubmed-article:9312049 | pubmed:abstractText | The success of a temperate bacteriophage is dependent upon its ability to completely shut down expression of its lytic genes during lysogenic growth. Mycobacteriophage L5 accomplishes this by an atypical phage repressor, gp71, which binds to multiple asymmetric DNA sites. L5 gp71 regulates transcription initiation at an early lytic promoter, Pleft, but also affects downstream gene expression at 'stoperator' sites in the phage genome. The L5 genome is replete with stoperator sites located within short intergenic spaces in both the early and late lytic operons and oriented specifically with respect to transcription. Binding of gp71 to these sites results in a strong orientation-dependent polar effect on downstream gene expression and global silencing of prophage gene expression. | lld:pubmed |
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| pubmed-article:9312049 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:9312049 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:9312049 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9312049 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:9312049 | pubmed:issn | 0261-4189 | lld:pubmed |
| pubmed-article:9312049 | pubmed:author | pubmed-author:BrownK LKL | lld:pubmed |
| pubmed-article:9312049 | pubmed:author | pubmed-author:WadsworthCC | lld:pubmed |
| pubmed-article:9312049 | pubmed:author | pubmed-author:HatfullG FGF | lld:pubmed |
| pubmed-article:9312049 | pubmed:author | pubmed-author:SarkisG JGJ | lld:pubmed |
| pubmed-article:9312049 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9312049 | pubmed:day | 1 | lld:pubmed |
| pubmed-article:9312049 | pubmed:volume | 16 | lld:pubmed |
| pubmed-article:9312049 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9312049 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9312049 | pubmed:pagination | 5914-21 | lld:pubmed |
| pubmed-article:9312049 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:9312049 | pubmed:meshHeading | pubmed-meshheading:9312049-... | lld:pubmed |
| pubmed-article:9312049 | pubmed:year | 1997 | lld:pubmed |
| pubmed-article:9312049 | pubmed:articleTitle | Transcriptional silencing by the mycobacteriophage L5 repressor. | lld:pubmed |
| pubmed-article:9312049 | pubmed:affiliation | Department of Biological Sciences, University of Pittsburgh, Pittsburgh, PA 15260, USA. | lld:pubmed |
| pubmed-article:9312049 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:9312049 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:9312049 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
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