Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
24
pubmed:dateCreated
1999-1-22
pubmed:abstractText
Transcriptional activation by c-Myc through specific E box elements is thought to be essential for its biological role. However, c-MycS is unable to activate transcription through these elements and yet retains the ability to stimulate proliferation, induce anchorage-independent growth, and induce apoptosis. In addition, c-MycS retains the ability to repress transcription of several specific promoters. Furthermore, c-MycS can rescue the c-myc null phenotype in fibroblasts with homozygous deletion of c-myc. Taken together, our data argue against the paradigm that all of the biological functions of c-Myc are mediated by transcriptional activation of specific target genes through E box elements.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/9869633-1406956, http://linkedlifedata.com/resource/pubmed/commentcorrection/9869633-1555236, http://linkedlifedata.com/resource/pubmed/commentcorrection/9869633-1628829, http://linkedlifedata.com/resource/pubmed/commentcorrection/9869633-2233723, http://linkedlifedata.com/resource/pubmed/commentcorrection/9869633-3299053, http://linkedlifedata.com/resource/pubmed/commentcorrection/9869633-7499403, http://linkedlifedata.com/resource/pubmed/commentcorrection/9869633-7784172, http://linkedlifedata.com/resource/pubmed/commentcorrection/9869633-7958908, http://linkedlifedata.com/resource/pubmed/commentcorrection/9869633-8076602, http://linkedlifedata.com/resource/pubmed/commentcorrection/9869633-8356088, http://linkedlifedata.com/resource/pubmed/commentcorrection/9869633-8494784, http://linkedlifedata.com/resource/pubmed/commentcorrection/9869633-8600028, http://linkedlifedata.com/resource/pubmed/commentcorrection/9869633-8692870, http://linkedlifedata.com/resource/pubmed/commentcorrection/9869633-9032273, http://linkedlifedata.com/resource/pubmed/commentcorrection/9869633-9054499, http://linkedlifedata.com/resource/pubmed/commentcorrection/9869633-9175477, http://linkedlifedata.com/resource/pubmed/commentcorrection/9869633-9190899, http://linkedlifedata.com/resource/pubmed/commentcorrection/9869633-9342182, http://linkedlifedata.com/resource/pubmed/commentcorrection/9869633-9371770, http://linkedlifedata.com/resource/pubmed/commentcorrection/9869633-9708738
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/GADD45 protein, http://linkedlifedata.com/resource/pubmed/chemical/GAS1 protein, S cerevisiae, http://linkedlifedata.com/resource/pubmed/chemical/Intracellular Signaling Peptides..., http://linkedlifedata.com/resource/pubmed/chemical/Membrane Glycoproteins, http://linkedlifedata.com/resource/pubmed/chemical/Ornithine Decarboxylase, http://linkedlifedata.com/resource/pubmed/chemical/Protein Isoforms, http://linkedlifedata.com/resource/pubmed/chemical/Protein Precursors, http://linkedlifedata.com/resource/pubmed/chemical/Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-myc, http://linkedlifedata.com/resource/pubmed/chemical/Repressor Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Saccharomyces cerevisiae Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Thymosin, http://linkedlifedata.com/resource/pubmed/chemical/prothymosin alpha
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0890-9369
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
12
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3803-8
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:9869633-3T3 Cells, pubmed-meshheading:9869633-Animals, pubmed-meshheading:9869633-Apoptosis, pubmed-meshheading:9869633-Cell Division, pubmed-meshheading:9869633-Cell Line, pubmed-meshheading:9869633-Cell Transformation, Neoplastic, pubmed-meshheading:9869633-Enhancer Elements, Genetic, pubmed-meshheading:9869633-Gene Expression Regulation, pubmed-meshheading:9869633-Genes, myc, pubmed-meshheading:9869633-Genes, p53, pubmed-meshheading:9869633-Intracellular Signaling Peptides and Proteins, pubmed-meshheading:9869633-Membrane Glycoproteins, pubmed-meshheading:9869633-Mice, pubmed-meshheading:9869633-Ornithine Decarboxylase, pubmed-meshheading:9869633-Phenotype, pubmed-meshheading:9869633-Protein Isoforms, pubmed-meshheading:9869633-Protein Precursors, pubmed-meshheading:9869633-Proteins, pubmed-meshheading:9869633-Proto-Oncogene Proteins c-myc, pubmed-meshheading:9869633-Rats, pubmed-meshheading:9869633-Repressor Proteins, pubmed-meshheading:9869633-Response Elements, pubmed-meshheading:9869633-Saccharomyces cerevisiae Proteins, pubmed-meshheading:9869633-Sequence Deletion, pubmed-meshheading:9869633-Thymosin, pubmed-meshheading:9869633-Transcriptional Activation, pubmed-meshheading:9869633-Transfection
pubmed:year
1998
pubmed:articleTitle
Transactivation-defective c-MycS retains the ability to regulate proliferation and apoptosis.
pubmed:affiliation
Department of Cell Biology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-2175 USA.
pubmed:publicationType
Journal Article