pubmed-article:7963517 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:7963517 | lifeskim:mentions | umls-concept:C0025914 | lld:lifeskim |
pubmed-article:7963517 | lifeskim:mentions | umls-concept:C0026809 | lld:lifeskim |
pubmed-article:7963517 | lifeskim:mentions | umls-concept:C0039194 | lld:lifeskim |
pubmed-article:7963517 | lifeskim:mentions | umls-concept:C0009015 | lld:lifeskim |
pubmed-article:7963517 | lifeskim:mentions | umls-concept:C0288331 | lld:lifeskim |
pubmed-article:7963517 | lifeskim:mentions | umls-concept:C1521991 | lld:lifeskim |
pubmed-article:7963517 | lifeskim:mentions | umls-concept:C1332397 | lld:lifeskim |
pubmed-article:7963517 | lifeskim:mentions | umls-concept:C1880022 | lld:lifeskim |
pubmed-article:7963517 | pubmed:issue | 10 | lld:pubmed |
pubmed-article:7963517 | pubmed:dateCreated | 1994-12-7 | lld:pubmed |
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pubmed-article:7963517 | pubmed:databankReference | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7963517 | pubmed:abstractText | We report the cloning and initial characterization of the mouse homologues of the bcl-2-related gene, bcl-x. We compare these to the two major isoforms of human bcl-x that were previously identified, bcl-xLong (bcl-xL) which has death repressor activity similar to bcl-2, and bcl-xShort (bcl-xS), an alternative mRNA splice product that deletes a highly conserved domain shared by bcl-2 family members and promotes cell death in transfection studies. In addition to murine (m) bcl-xL and mbcl-xS, we have cloned a novel cDNA isoform that we designate mbcl-x delta TM. This cDNA deletes, by means of alternative splicing, the carboxy terminal transmembrane domain of bcl-x and is predicted to be a soluble, rather than membrane-bound, protein. We found that mbcl-x mRNA is highly inducible in splenocytes stimulated with either anti-CD3 Abs or LPS/dextran sulfate, and that the major species of mbcl-x mRNA in a variety of cell lines and tissues was the xL isoform. Transfection of mbcl-xL or mbcl-xS into Hela cells resulted in targeting primarily to mitochondria, whereas mbcl-x delta TM localized diffusely throughout the cytosol. Overexpression of the novel delta TM isoform in an IL-3-dependent cell line delayed the onset of apoptosis induced by growth factor withdrawal. Thus, a naturally-occurring form of mbcl-x present in lymphocytes that does not localize to the mitochondrial membrane is functional in preventing apoptotic cell death. Moreover, these data suggest that bcl-x provides a life signal in activated lymphocytes. | lld:pubmed |
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pubmed-article:7963517 | pubmed:language | eng | lld:pubmed |
pubmed-article:7963517 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7963517 | pubmed:citationSubset | AIM | lld:pubmed |
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pubmed-article:7963517 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:7963517 | pubmed:month | Nov | lld:pubmed |
pubmed-article:7963517 | pubmed:issn | 0022-1767 | lld:pubmed |
pubmed-article:7963517 | pubmed:author | pubmed-author:MuellerD LDL | lld:pubmed |
pubmed-article:7963517 | pubmed:author | pubmed-author:DartL HLHJr | lld:pubmed |
pubmed-article:7963517 | pubmed:author | pubmed-author:BehrensT WTW | lld:pubmed |
pubmed-article:7963517 | pubmed:author | pubmed-author:RivardJ JJJ | lld:pubmed |
pubmed-article:7963517 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:7963517 | pubmed:day | 15 | lld:pubmed |
pubmed-article:7963517 | pubmed:volume | 153 | lld:pubmed |
pubmed-article:7963517 | pubmed:geneSymbol | bcl-x | lld:pubmed |
pubmed-article:7963517 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:7963517 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:7963517 | pubmed:pagination | 4388-98 | lld:pubmed |
pubmed-article:7963517 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
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pubmed-article:7963517 | pubmed:year | 1994 | lld:pubmed |
pubmed-article:7963517 | pubmed:articleTitle | Cloning and molecular characterization of mouse bcl-x in B and T lymphocytes. | lld:pubmed |
pubmed-article:7963517 | pubmed:affiliation | Department of Medicine/Rheumatology, University of Minnesota, Minneapolis 55455. | lld:pubmed |
pubmed-article:7963517 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:7963517 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:7963517 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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