| pubmed-article:7623806 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:7623806 | lifeskim:mentions | umls-concept:C1524059 | lld:lifeskim |
| pubmed-article:7623806 | lifeskim:mentions | umls-concept:C0031327 | lld:lifeskim |
| pubmed-article:7623806 | lifeskim:mentions | umls-concept:C0009015 | lld:lifeskim |
| pubmed-article:7623806 | lifeskim:mentions | umls-concept:C0205245 | lld:lifeskim |
| pubmed-article:7623806 | lifeskim:mentions | umls-concept:C1336776 | lld:lifeskim |
| pubmed-article:7623806 | lifeskim:mentions | umls-concept:C1880022 | lld:lifeskim |
| pubmed-article:7623806 | pubmed:issue | 8 | lld:pubmed |
| pubmed-article:7623806 | pubmed:dateCreated | 1995-8-29 | lld:pubmed |
| pubmed-article:7623806 | pubmed:abstractText | Biochemical purification and cognate cDNA cloning studies have revealed that the previously described transcriptional coactivator OCA-B consists of a 34- or 35-kDa polypeptide with sequence relationships to known coactivators that function by protein-protein interactions. Studies with a recombinant protein have proved that a single OCA-B polypeptide is the main determinant for B-cell-specific activation of immunoglobulin (Ig) promoters and provided additional insights into its mechanism of action. Recombinant OCA-B can function equally well with Oct-1 or Oct-2 on an Ig promoter, but while corresponding POU domains are sufficient for OCA-B interaction, and for octamer-mediated transcription of a histone H2B promoter, an additional Oct-1 or Oct-2 activation domain(s) is necessary for functional synergy with OCA-B. Further studies additional Oct-1 or Oct-2 activation domain(s) is necessary for functional synergy with OCA-B. Further studies show that Ig promoter activation by Oct-1 and OCA-B requires still other general (USA-derived) cofactors and also provide indirect evidence that distinct Oct-interacting cofactors regulate H2B transcription. | lld:pubmed |
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| pubmed-article:7623806 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:7623806 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:7623806 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:7623806 | pubmed:month | Aug | lld:pubmed |
| pubmed-article:7623806 | pubmed:issn | 0270-7306 | lld:pubmed |
| pubmed-article:7623806 | pubmed:author | pubmed-author:RoederR GRG | lld:pubmed |
| pubmed-article:7623806 | pubmed:author | pubmed-author:LuoYY | lld:pubmed |
| pubmed-article:7623806 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:7623806 | pubmed:volume | 15 | lld:pubmed |
| pubmed-article:7623806 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:7623806 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:7623806 | pubmed:pagination | 4115-24 | lld:pubmed |
| pubmed-article:7623806 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:7623806 | pubmed:year | 1995 | lld:pubmed |
| pubmed-article:7623806 | pubmed:articleTitle | Cloning, functional characterization, and mechanism of action of the B-cell-specific transcriptional coactivator OCA-B. | lld:pubmed |
| pubmed-article:7623806 | pubmed:affiliation | Laboratory of Biochemistry and Molecular Biology, Rockefeller University, New York, New York 10021, USA. | lld:pubmed |
| pubmed-article:7623806 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:7623806 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:7623806 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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