| pubmed-article:9417108 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9417108 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
| pubmed-article:9417108 | lifeskim:mentions | umls-concept:C1704675 | lld:lifeskim |
| pubmed-article:9417108 | lifeskim:mentions | umls-concept:C0162493 | lld:lifeskim |
| pubmed-article:9417108 | lifeskim:mentions | umls-concept:C1419258 | lld:lifeskim |
| pubmed-article:9417108 | lifeskim:mentions | umls-concept:C0086860 | lld:lifeskim |
| pubmed-article:9417108 | lifeskim:mentions | umls-concept:C0026377 | lld:lifeskim |
| pubmed-article:9417108 | lifeskim:mentions | umls-concept:C1521761 | lld:lifeskim |
| pubmed-article:9417108 | lifeskim:mentions | umls-concept:C1523987 | lld:lifeskim |
| pubmed-article:9417108 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:9417108 | pubmed:dateCreated | 1998-2-3 | lld:pubmed |
| pubmed-article:9417108 | pubmed:abstractText | The murine Htf9-a/RanBP1 and Htf9-c genes are divergently transcribed from a shared TATA-less promoter. Transcription of both genes is initiated on complementary DNA strands and is controlled by cell cycle-dependent mechanisms. The bidirectional promoter harbors a genomic footprint flanking the major transcription start site of both genes. Transient promoter assays showed that the footprinted element is important for transcription of both genes. Protein-binding experiments and antibody assays indicated that members of the retinoid X receptor family interact with the double-stranded site. In addition, distinct factors interact with single DNA strands of the element. Double-stranded binding factors were highly expressed in liver cells, in which neither gene is transcribed, while single-stranded binding proteins were abundant in cycling cells, in which transcription of both genes is efficient. In vivo S1 analysis of the promoter depicted an S1-sensitive organization in cells in which transcription of both genes is active; S1 sensitivity was not detected in conditions of transcriptional repression. Thus, the same element is a target for either retinoid X receptor factors, or for single-stranded binding proteins, and form distinct complexes in different cellular conditions depending on the DNA conformation in the binding site. | lld:pubmed |
| pubmed-article:9417108 | pubmed:language | eng | lld:pubmed |
| pubmed-article:9417108 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9417108 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:9417108 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9417108 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9417108 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9417108 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:9417108 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9417108 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9417108 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9417108 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9417108 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9417108 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9417108 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9417108 | pubmed:month | Jan | lld:pubmed |
| pubmed-article:9417108 | pubmed:issn | 0021-9258 | lld:pubmed |
| pubmed-article:9417108 | pubmed:author | pubmed-author:Di MatteoGG | lld:pubmed |
| pubmed-article:9417108 | pubmed:author | pubmed-author:PalittiFF | lld:pubmed |
| pubmed-article:9417108 | pubmed:author | pubmed-author:SalernoMM | lld:pubmed |
| pubmed-article:9417108 | pubmed:author | pubmed-author:LaviaPP | lld:pubmed |
| pubmed-article:9417108 | pubmed:author | pubmed-author:GuarguagliniG... | lld:pubmed |
| pubmed-article:9417108 | pubmed:author | pubmed-author:Di FioreBB | lld:pubmed |
| pubmed-article:9417108 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9417108 | pubmed:day | 2 | lld:pubmed |
| pubmed-article:9417108 | pubmed:volume | 273 | lld:pubmed |
| pubmed-article:9417108 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9417108 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9417108 | pubmed:pagination | 495-505 | lld:pubmed |
| pubmed-article:9417108 | pubmed:dateRevised | 2008-11-21 | lld:pubmed |
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| pubmed-article:9417108 | pubmed:year | 1998 | lld:pubmed |
| pubmed-article:9417108 | pubmed:articleTitle | Interactions with single-stranded and double-stranded DNA-binding factors and alternative promoter conformation upon transcriptional activation of the Htf9-a/RanBP1 and Htf9-c genes. | lld:pubmed |
| pubmed-article:9417108 | pubmed:affiliation | CNR Centre of Evolutionary Genetics, c/o Department of Genetics and Molecular Biology, University "La Sapienza," Rome 00185, Italy. | lld:pubmed |
| pubmed-article:9417108 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:9417108 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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