pubmed-article:1406647 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:1406647 | lifeskim:mentions | umls-concept:C0930565 | lld:lifeskim |
pubmed-article:1406647 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
pubmed-article:1406647 | lifeskim:mentions | umls-concept:C0040649 | lld:lifeskim |
pubmed-article:1406647 | lifeskim:mentions | umls-concept:C0086860 | lld:lifeskim |
pubmed-article:1406647 | lifeskim:mentions | umls-concept:C0013139 | lld:lifeskim |
pubmed-article:1406647 | lifeskim:mentions | umls-concept:C0936012 | lld:lifeskim |
pubmed-article:1406647 | lifeskim:mentions | umls-concept:C1515655 | lld:lifeskim |
pubmed-article:1406647 | pubmed:issue | 10 | lld:pubmed |
pubmed-article:1406647 | pubmed:dateCreated | 1992-10-26 | lld:pubmed |
pubmed-article:1406647 | pubmed:abstractText | Transcriptional regulation of the TATA-less promoter of the Drosophila melanogaster vermilion (v) gene was investigated. Developmental Northern (RNA) blot analysis showed that v transcripts accumulate during late embryo, larval, and adult stages. Sequences that control expression in adults were delineated by analyzing a series of 5' and 3' deletion constructions after germ line transformation. These studies defined two regions, -300 to -600 and -60 to -160, relative to the major transcription start site, as important for maximal levels of expression. Analysis of transformants bearing v-lacZ promoter fusions showed that larval expression is fat body specific and that expression depends on sequences located between +19 and +36 downstream of transcription start site. This downstream element can be functionally replaced by a TATA box in vivo. Furthermore, when added to the wild-type v promoter, a TATA element augments the level of v transcription by three- to fivefold. | lld:pubmed |
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pubmed-article:1406647 | pubmed:language | eng | lld:pubmed |
pubmed-article:1406647 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1406647 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:1406647 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:1406647 | pubmed:month | Oct | lld:pubmed |
pubmed-article:1406647 | pubmed:issn | 0270-7306 | lld:pubmed |
pubmed-article:1406647 | pubmed:author | pubmed-author:SearlesL LLL | lld:pubmed |
pubmed-article:1406647 | pubmed:author | pubmed-author:FridellY WYW | lld:pubmed |
pubmed-article:1406647 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:1406647 | pubmed:volume | 12 | lld:pubmed |
pubmed-article:1406647 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:1406647 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:1406647 | pubmed:pagination | 4571-7 | lld:pubmed |
pubmed-article:1406647 | pubmed:dateRevised | 2010-9-7 | lld:pubmed |
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pubmed-article:1406647 | pubmed:year | 1992 | lld:pubmed |
pubmed-article:1406647 | pubmed:articleTitle | In vivo transcriptional analysis of the TATA-less promoter of the Drosophila melanogaster vermilion gene. | lld:pubmed |
pubmed-article:1406647 | pubmed:affiliation | Department of Biology, University of North Carolina, Chapel Hill 27599-3280. | lld:pubmed |
pubmed-article:1406647 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:1406647 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
entrez-gene:32026 | entrezgene:pubmed | pubmed-article:1406647 | lld:entrezgene |
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