Source:http://linkedlifedata.com/resource/pubmed/id/10815807
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
17
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pubmed:dateCreated |
2000-6-8
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pubmed:abstractText |
The c-Myb proto-oncogene is preferentially expressed in hematopoietic lineages, and highly expressed in several leukemia types. The Human T-cell Leukemia Virus Type I (HTLV-I) is the etiological agent of Adult T-cell Leukemia/Lymphoma (ATLL). A previous report suggested that Tax, the viral transactivator, is able to suppress the transactivation potential of c-Myb protein by competing for recruitment of CBP. We tested whether such a competition could affect transcription from the c-Myb promoter in Tax expressing T-cells. Using several c-Myb promoter reporter constructs carrying mutations in various regions, we demonstrate that Tax suppression of c-Myb transactivation results in transrepression of the c-Myb promoter through the Myb responsive elements in Jurkat T-cells. The ability of Tax mutants M22, M47 and V89A to interact with the full-length CBP and p300 proteins in vitro, and their ability to repress the c-Myb promoter, was then evaluated. Although both M47 and M22 bind to CBP and p300 to a similar extent, only M47 was able to repress the c-Myb promoter, suggesting that competition for CBP/p300 binding was not the mechanism underlying Tax's effect. This concept was further supported by the fact that the Tax mutant V89A transrepresses the c-Myb promoter efficiently in spite of an impaired binding to CBP and p300. Therefore, Tax-mediated repression of the c-Myb promoter appears to be independent from a direct competition between c-Myb and Tax for recruitment of CBP/p300. Interestingly, a decreased transcription from the endogenous c-Myb promoter was observed in several HTLV-I transformed T-cell lines. Finally, the ability of Tax to directly repress the endogenous c-Myb promoter was demonstrated in a Jurkat cell line stably transfected with a tax gene driven by a cadmium-inducible promoter.
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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/CREB-Binding Protein,
http://linkedlifedata.com/resource/pubmed/chemical/CREBBP protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclic AMP Response...,
http://linkedlifedata.com/resource/pubmed/chemical/Gene Products, tax,
http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-myb,
http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0950-9232
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
20
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pubmed:volume |
19
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2155-64
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:10815807-CREB-Binding Protein,
pubmed-meshheading:10815807-Cell Line, Transformed,
pubmed-meshheading:10815807-Cell Transformation, Viral,
pubmed-meshheading:10815807-Cyclic AMP Response Element-Binding Protein,
pubmed-meshheading:10815807-Gene Products, tax,
pubmed-meshheading:10815807-Human T-lymphotropic virus 1,
pubmed-meshheading:10815807-Humans,
pubmed-meshheading:10815807-Jurkat Cells,
pubmed-meshheading:10815807-Mutation,
pubmed-meshheading:10815807-Nuclear Proteins,
pubmed-meshheading:10815807-Promoter Regions, Genetic,
pubmed-meshheading:10815807-Proto-Oncogene Proteins c-myb,
pubmed-meshheading:10815807-Response Elements,
pubmed-meshheading:10815807-Trans-Activators,
pubmed-meshheading:10815807-Transcription, Genetic
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pubmed:year |
2000
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pubmed:articleTitle |
HTLV-I Tax transrepresses the human c-Myb promoter independently of its interaction with CBP or p300.
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pubmed:affiliation |
Basic Research Laboratory, National Cancer Institute, Bethesda, Maryland 20814, USA.
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pubmed:publicationType |
Journal Article
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