Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
2005-9-22
pubmed:databankReference
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/GSM43979, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/GSM43980, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/GSM43981, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/GSM43982, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/GSM43983, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/GSM43984, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/GSM43985, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/GSM43986, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/GSM43987, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/GSM43988, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/GSM43989, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/GSM43990, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/GSM43991, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/GSM43992, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/GSM43993, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/GSM43994, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/GSM43995, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/GSM43996, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/GSM43997, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/GSM43998, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/GSM43999, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/GSM44000, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/GSM44001, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/GSM44002
pubmed:abstractText
The BCL6 proto-oncogene encodes a transcriptional repressor that is required for germinal center formation and has been linked to lymphomagenesis. BCL6 functions by directly binding to specific DNA sequences and suppressing the transcription of target genes. Here we report an alternative mechanism by which BCL6 controls the transcription of genes lacking a BCL6 binding site and show that this mechanism was required for the prevention of tumor suppressor p53-independent cell cycle arrest in germinal center B cells. BCL6 interacted with the transcriptional activator Miz-1 and, via Miz-1, bound to the promoter and suppressed transcription of the cell cycle arrest gene CDKN1A. Through this mechanism, BCL6 may facilitate the proliferative expansion of germinal centers during the normal immune response and, when deregulated, the pathological expansion of B cell lymphomas.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
1529-2908
pubmed:author
pubmed:issnType
Print
pubmed:volume
6
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1054-60
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:16142238-B-Lymphocytes, pubmed-meshheading:16142238-Cell Cycle, pubmed-meshheading:16142238-Cell Cycle Proteins, pubmed-meshheading:16142238-Cell Division, pubmed-meshheading:16142238-Cell Line, pubmed-meshheading:16142238-Cyclin-Dependent Kinase Inhibitor p21, pubmed-meshheading:16142238-DNA-Binding Proteins, pubmed-meshheading:16142238-Enzyme Inhibitors, pubmed-meshheading:16142238-Germinal Center, pubmed-meshheading:16142238-Humans, pubmed-meshheading:16142238-Kruppel-Like Transcription Factors, pubmed-meshheading:16142238-Molecular Sequence Data, pubmed-meshheading:16142238-Promoter Regions, Genetic, pubmed-meshheading:16142238-Proto-Oncogene Proteins, pubmed-meshheading:16142238-Proto-Oncogene Proteins c-bcl-6, pubmed-meshheading:16142238-Transcription, Genetic, pubmed-meshheading:16142238-Transcription Factors, pubmed-meshheading:16142238-Zinc Fingers
pubmed:year
2005
pubmed:articleTitle
BCL6 interacts with the transcription factor Miz-1 to suppress the cyclin-dependent kinase inhibitor p21 and cell cycle arrest in germinal center B cells.
pubmed:affiliation
Institute for Cancer Genetics, Department of Pathology, Herbert Irving Comprehensive Cancer Center, Columbia University, New York, New York 10032, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural