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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1996-12-20
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pubmed:databankReference |
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF004427,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF004428,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF004429,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF004430,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/U44426,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/U44427,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/U44428,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/U44429
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pubmed:abstractText |
Cloning is reported of a cDNA homologue to the breast carcinoma-associated D52 cDNA, termed D53, and of a mouse D52 cDNA (HGMW-approved symbols TPD52L1 and TPD52). Human D53 and mouse D52 proteins are predicted to be 52 and 86% identical to human D52, respectively. Analysis of the three protein sequences identified a coiled-coil domain and N- and C-terminally located PEST domains in each. The conservation of homology between the D52 and the D53 sequences, combined with a lack of homology between these and known proteins, defines a new mammalian gene/protein family, the D52 family. The human D52 locus has been previously mapped to chromosome 8q21, and using in situ mapping in the present study, a human D53 locus was mapped to chromosome 6q22-q23. We observed coexpression of the human D52 and D53 genes in some breast tumors and derivative cell lines and found that maintenance of D52 and D53 transcript levels in estrogen receptor-positive MCF7 breast carcinoma cells depends upon estradiol. However, D52 and D53 genes were specifically expressed in HL-60 and K-562 leukemia cells, respectively, with 12-O-tetra-decanoylphorbol-13-acetate treatment decreasing D52 and D53 transcript levels in these cell lines. The presence of a coiled-coil domain, combined with observed co- or independent expression of the D52 and D53 genes, suggests that D52 and D53 proteins may be capable of hetero- and/or homodimer formation.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0888-7543
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
35
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
523-32
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:8812487-Amino Acid Sequence,
pubmed-meshheading:8812487-Animals,
pubmed-meshheading:8812487-Base Sequence,
pubmed-meshheading:8812487-Breast,
pubmed-meshheading:8812487-Breast Neoplasms,
pubmed-meshheading:8812487-Cell Differentiation,
pubmed-meshheading:8812487-Chromosome Mapping,
pubmed-meshheading:8812487-Chromosomes, Human, Pair 6,
pubmed-meshheading:8812487-Cloning, Molecular,
pubmed-meshheading:8812487-DNA, Complementary,
pubmed-meshheading:8812487-Female,
pubmed-meshheading:8812487-HL-60 Cells,
pubmed-meshheading:8812487-Humans,
pubmed-meshheading:8812487-Mice,
pubmed-meshheading:8812487-Molecular Sequence Data,
pubmed-meshheading:8812487-Neoplasm Proteins,
pubmed-meshheading:8812487-Sequence Homology, Amino Acid,
pubmed-meshheading:8812487-Tumor Cells, Cultured
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pubmed:year |
1996
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pubmed:articleTitle |
Definition of the tumor protein D52 (TPD52) gene family through cloning of D52 homologues in human (hD53) and mouse (mD52).
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pubmed:affiliation |
Institut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS/INSERM/ULP, Illkirch, C.U. de Strasbourg, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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