Matches in SemOpenAlex for { <https://semopenalex.org/work/W1987910138> ?p ?o ?g. }
- W1987910138 endingPage "20936" @default.
- W1987910138 startingPage "20930" @default.
- W1987910138 abstract "Binding sites for the tissue-specific transcription factor, Pit-1, are required for basal and hormonally induced prolactin gene transcription. Although Pit-1 is phosphorylated in response to several signaling pathways, the mechanism by which Pit-1 contributes to hormonal induction of gene transcription has not been defined. Recent reports suggest that phosphorylation of Pit-1 may not be required for hormonal regulation of the prolactin promoter. Analysis of the contribution of individual Pit-1 binding sites has been complicated due to the fact that some of the elements appear to be redundant. To better understand the role of Pit-1 sites in mediating hormonal regulation of the prolactin gene, we have performed enhancer tests using the three most proximal Pit-1 binding sites of the rat prolactin gene which are designated the 1P, 2P, and 3P sites. The results demonstrate that multimers of the 3P Pit-1 binding site are much more responsive to several hormonal and intracellular signaling pathways than multimers of the 1P or 2P sites. The 3P DNA element was found to contain a consensus binding site for the Ets family of proteins. Mutation of the Ets binding site greatly decreased the ability of epidermal growth factor, phorbol esters, Ras, or the Raf kinase to induce reporter gene activity. Mutation of the Ets site had little effect on basal enhancer activity. In contrast, mutation of the consensus Pit-1 binding site in the 3P element essentially abolished all basal enhancer activity. Overexpression of Ets-1 in GH<sub>3</sub> pituitary cells enhanced both basal and Ras induced activity from the 3P enhancer. These data describe a composite element in the prolactin gene containing binding sites for two different factors and the studies suggest a mechanism by which Ets proteins and Pit-1 functionally cooperate to permit transcriptional regulation by different signaling pathways." @default.
- W1987910138 created "2016-06-24" @default.
- W1987910138 creator A5047866081 @default.
- W1987910138 creator A5055159286 @default.
- W1987910138 date "1995-09-01" @default.
- W1987910138 modified "2023-10-14" @default.
- W1987910138 title "A Composite Ets/Pit-1 Binding Site in the Prolactin Gene Can Mediate Transcriptional Responses to Multiple Signal Transduction Pathways" @default.
- W1987910138 cites W1488876668 @default.
- W1987910138 cites W1503726340 @default.
- W1987910138 cites W1559986791 @default.
- W1987910138 cites W1567128643 @default.
- W1987910138 cites W1581572500 @default.
- W1987910138 cites W1583056254 @default.
- W1987910138 cites W1583894029 @default.
- W1987910138 cites W1594412667 @default.
- W1987910138 cites W1601455272 @default.
- W1987910138 cites W1608533627 @default.
- W1987910138 cites W1648689484 @default.
- W1987910138 cites W1661830960 @default.
- W1987910138 cites W1678773327 @default.
- W1987910138 cites W1965164352 @default.
- W1987910138 cites W1966751687 @default.
- W1987910138 cites W1968835154 @default.
- W1987910138 cites W1969785844 @default.
- W1987910138 cites W1970132032 @default.
- W1987910138 cites W1971980406 @default.
- W1987910138 cites W1990097058 @default.
- W1987910138 cites W1991247661 @default.
- W1987910138 cites W1994124188 @default.
- W1987910138 cites W1998737642 @default.
- W1987910138 cites W2000082154 @default.
- W1987910138 cites W2012959255 @default.
- W1987910138 cites W2026606309 @default.
- W1987910138 cites W2029177264 @default.
- W1987910138 cites W2034454625 @default.
- W1987910138 cites W2037745464 @default.
- W1987910138 cites W2047466377 @default.
- W1987910138 cites W2051731919 @default.
- W1987910138 cites W2052366220 @default.
- W1987910138 cites W2062617470 @default.
- W1987910138 cites W2063206483 @default.
- W1987910138 cites W2064419581 @default.
- W1987910138 cites W2064557280 @default.
- W1987910138 cites W2068571186 @default.
- W1987910138 cites W2079045007 @default.
- W1987910138 cites W2080924363 @default.
- W1987910138 cites W2083402068 @default.
- W1987910138 cites W2085996016 @default.
- W1987910138 cites W2090127766 @default.
- W1987910138 cites W2108415605 @default.
- W1987910138 cites W2126400723 @default.
- W1987910138 cites W2133508418 @default.
- W1987910138 cites W2139476145 @default.
- W1987910138 cites W2141343816 @default.
- W1987910138 cites W2145330934 @default.
- W1987910138 cites W2148750115 @default.
- W1987910138 cites W2149243417 @default.
- W1987910138 cites W2156076143 @default.
- W1987910138 cites W2169377140 @default.
- W1987910138 cites W2171569176 @default.
- W1987910138 cites W7299164 @default.
- W1987910138 cites W912507531 @default.
- W1987910138 cites W99079292 @default.
- W1987910138 cites W2056948143 @default.
- W1987910138 doi "https://doi.org/10.1074/jbc.270.36.20930" @default.
- W1987910138 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/7673116" @default.
- W1987910138 hasPublicationYear "1995" @default.
- W1987910138 type Work @default.
- W1987910138 sameAs 1987910138 @default.
- W1987910138 citedByCount "62" @default.
- W1987910138 countsByYear W19879101382015 @default.
- W1987910138 countsByYear W19879101382017 @default.
- W1987910138 crossrefType "journal-article" @default.
- W1987910138 hasAuthorship W1987910138A5047866081 @default.
- W1987910138 hasAuthorship W1987910138A5055159286 @default.
- W1987910138 hasBestOaLocation W19879101381 @default.
- W1987910138 hasConcept C104317684 @default.
- W1987910138 hasConcept C107824862 @default.
- W1987910138 hasConcept C111936080 @default.
- W1987910138 hasConcept C11960822 @default.
- W1987910138 hasConcept C134018914 @default.
- W1987910138 hasConcept C138885662 @default.
- W1987910138 hasConcept C150194340 @default.
- W1987910138 hasConcept C153911025 @default.
- W1987910138 hasConcept C161733203 @default.
- W1987910138 hasConcept C179926584 @default.
- W1987910138 hasConcept C2779064019 @default.
- W1987910138 hasConcept C41895202 @default.
- W1987910138 hasConcept C54355233 @default.
- W1987910138 hasConcept C62478195 @default.
- W1987910138 hasConcept C71315377 @default.
- W1987910138 hasConcept C86339819 @default.
- W1987910138 hasConcept C86803240 @default.
- W1987910138 hasConcept C95444343 @default.
- W1987910138 hasConceptScore W1987910138C104317684 @default.
- W1987910138 hasConceptScore W1987910138C107824862 @default.
- W1987910138 hasConceptScore W1987910138C111936080 @default.
- W1987910138 hasConceptScore W1987910138C11960822 @default.