| pubmed-article:3582369 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:3582369 | lifeskim:mentions | umls-concept:C0086418 | lld:lifeskim |
| pubmed-article:3582369 | lifeskim:mentions | umls-concept:C0043342 | lld:lifeskim |
| pubmed-article:3582369 | lifeskim:mentions | umls-concept:C1706383 | lld:lifeskim |
| pubmed-article:3582369 | lifeskim:mentions | umls-concept:C0205145 | lld:lifeskim |
| pubmed-article:3582369 | lifeskim:mentions | umls-concept:C0010853 | lld:lifeskim |
| pubmed-article:3582369 | lifeskim:mentions | umls-concept:C0001271 | lld:lifeskim |
| pubmed-article:3582369 | lifeskim:mentions | umls-concept:C0085940 | lld:lifeskim |
| pubmed-article:3582369 | lifeskim:mentions | umls-concept:C0086860 | lld:lifeskim |
| pubmed-article:3582369 | lifeskim:mentions | umls-concept:C0237876 | lld:lifeskim |
| pubmed-article:3582369 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:3582369 | pubmed:dateCreated | 1987-7-16 | lld:pubmed |
| pubmed-article:3582369 | pubmed:abstractText | Xenopus laevis cytoskeletal actin gene promoters contain a 20-bp sequence homologous to the serum response element (SRE) required for transient human c-fos gene transcription in response to serum factors. Both sequences bind the same factor in HeLa cell extracts, as shown by binding competition, DNase I and dimethylsulphate (DMS) protection and DMS interference assays. A similar protein is present in Xenopus laevis oocytes. Sequences containing the SRE homology are essential for constitutive activity of the actin promoter in both Xenopus and mouse cells, and a synthetic SRE functions as a promoter element in these cells. In mouse cells, transcription of both transfected Xenopus actin and actin/c-fos fusion genes is activated following serum stimulation. These data suggest that the SRE and its cognate protein form part of a regulatory pathway that has been highly conserved during evolution. | lld:pubmed |
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| pubmed-article:3582369 | pubmed:language | eng | lld:pubmed |
| pubmed-article:3582369 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:3582369 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:3582369 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:3582369 | pubmed:month | Mar | lld:pubmed |
| pubmed-article:3582369 | pubmed:issn | 0261-4189 | lld:pubmed |
| pubmed-article:3582369 | pubmed:author | pubmed-author:TreismanRR | lld:pubmed |
| pubmed-article:3582369 | pubmed:author | pubmed-author:GarrettNN | lld:pubmed |
| pubmed-article:3582369 | pubmed:author | pubmed-author:MohunTT | lld:pubmed |
| pubmed-article:3582369 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:3582369 | pubmed:volume | 6 | lld:pubmed |
| pubmed-article:3582369 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:3582369 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:3582369 | pubmed:pagination | 667-73 | lld:pubmed |
| pubmed-article:3582369 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:3582369 | pubmed:year | 1987 | lld:pubmed |
| pubmed-article:3582369 | pubmed:articleTitle | Xenopus cytoskeletal actin and human c-fos gene promoters share a conserved protein-binding site. | lld:pubmed |
| pubmed-article:3582369 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:3582369 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:3582369 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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