rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1-2
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pubmed:dateCreated |
2008-4-8
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pubmed:abstractText |
The LAT gene encodes an adaptor molecule that links receptor engagement to critical downstream signaling events. Previously, we identified the proximal promoter for the human LAT gene and found that it contains binding sites for members of the Ets and Runx transcription factor families. In the present study, we show that the promoter also contains 5 GC-rich elements that contribute to promoter activity and that are capable of binding the transcription factors Sp1 and Sp3. Overexpression of either Sp1 or full-length Sp3 was shown to augment LAT promoter activity, while siRNA-mediated knockdown of each transcription factor was demonstrated to have an inhibitory effect. We also discovered a cell-type specific DNase hypersensitive site that maps to the Sp1/Sp3 and adjacent Ets and Runx binding sites. Collectively, these results provide compelling data that implicates Sp1 and Sp3 in the transcriptional regulation of the human LAT gene.
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Adaptor Proteins, Signal Transducing,
http://linkedlifedata.com/resource/pubmed/chemical/DNA,
http://linkedlifedata.com/resource/pubmed/chemical/LAT protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Small Interfering,
http://linkedlifedata.com/resource/pubmed/chemical/SP3 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Sp1 Transcription Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Sp3 Transcription Factor
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0378-1119
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pubmed:author |
|
pubmed:issnType |
Print
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pubmed:day |
30
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pubmed:volume |
413
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
58-66
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:18343609-Adaptor Proteins, Signal Transducing,
pubmed-meshheading:18343609-Animals,
pubmed-meshheading:18343609-Base Sequence,
pubmed-meshheading:18343609-Binding Sites,
pubmed-meshheading:18343609-Cell Line,
pubmed-meshheading:18343609-DNA,
pubmed-meshheading:18343609-Drosophila,
pubmed-meshheading:18343609-GC Rich Sequence,
pubmed-meshheading:18343609-HeLa Cells,
pubmed-meshheading:18343609-Humans,
pubmed-meshheading:18343609-Jurkat Cells,
pubmed-meshheading:18343609-Membrane Proteins,
pubmed-meshheading:18343609-Molecular Sequence Data,
pubmed-meshheading:18343609-Mutagenesis, Site-Directed,
pubmed-meshheading:18343609-Promoter Regions, Genetic,
pubmed-meshheading:18343609-RNA, Small Interfering,
pubmed-meshheading:18343609-Regulatory Elements, Transcriptional,
pubmed-meshheading:18343609-Sp1 Transcription Factor,
pubmed-meshheading:18343609-Sp3 Transcription Factor,
pubmed-meshheading:18343609-Transcription, Genetic
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pubmed:year |
2008
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pubmed:articleTitle |
Transcription of the LAT gene is regulated by multiple binding sites for Sp1 and Sp3.
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pubmed:affiliation |
Agnes Scott College, Department of Biology, 141 E. College Ave., Decatur, GA 30030, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.
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