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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
1995-3-2
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pubmed:databankReference | |
pubmed:abstractText |
In primary rodent cells transformed by the E1A region of the highly oncogenic adenovirus type 12, repression of transcription mediated by the far upstream TATA-like element was observed only in conjunction with either possible juxtaposition of a CAA repeated element in the presence of E1A and was dependent upon the relative arrangement of both the TATA-like and CAA repeated motifs in both homologous and heterologous promoter constructs. A gel shift competition study demonstrated that the TATA-binding protein (TBP) or a TBP-like protein can bind to both the upstream TATA-like sequence and the regular TATA box on the H-2Kb basal promoter. Moreover, employing immunoselection and cyclic amplification and selection of targets (CASTing) methods with nuclear extracts derived from Ad12-E1A transformants, we have identified a high affinity binding site in the H-2Kb class I promoter for E1A-associated DNA-binding proteins. The sequences of the binding sites were identified and were found to contain both the upstream TATA-like motif and the CAA repeated motifs. Our results suggest that the TATA-like sequence in the far upstream region of the H-2Kb gene is one of the elements that is required for Ad12-E1A-mediated negative repression.
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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/Adenovirus E1A Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/H-2 Antigens,
http://linkedlifedata.com/resource/pubmed/chemical/H-2Kb protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Repressor Proteins
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0021-9258
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
3
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pubmed:volume |
270
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pubmed:owner |
NLM
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pubmed:authorsComplete |
N
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pubmed:pagination |
2327-36
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:7836466-Adenovirus E1A Proteins,
pubmed-meshheading:7836466-Animals,
pubmed-meshheading:7836466-Base Sequence,
pubmed-meshheading:7836466-Binding, Competitive,
pubmed-meshheading:7836466-Cell Transformation, Viral,
pubmed-meshheading:7836466-DNA-Binding Proteins,
pubmed-meshheading:7836466-Gene Expression Regulation,
pubmed-meshheading:7836466-H-2 Antigens,
pubmed-meshheading:7836466-Mice,
pubmed-meshheading:7836466-Molecular Sequence Data,
pubmed-meshheading:7836466-Promoter Regions, Genetic,
pubmed-meshheading:7836466-RNA, Messenger,
pubmed-meshheading:7836466-Regulatory Sequences, Nucleic Acid,
pubmed-meshheading:7836466-Repetitive Sequences, Nucleic Acid,
pubmed-meshheading:7836466-Repressor Proteins,
pubmed-meshheading:7836466-TATA Box,
pubmed-meshheading:7836466-Transcription, Genetic
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pubmed:year |
1995
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pubmed:articleTitle |
Cooperatively between an upstream TATA-like sequence and a CAA repeated element mediates E1A-dependent negative repression of the H-2Kb class I gene.
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pubmed:affiliation |
Tsukuba Life Science Center, RIKEN (Institute of Physical and Chemical Research), Ibaraki, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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