Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
54
pubmed:dateCreated
2001-2-22
pubmed:abstractText
Most acute promyelocytic leukemia (APL) cases are associated with recurrent translocations between the gene of retinoic receptor alpha and that of PML (t(15;17)) or PLZF (t(11;17)). PML localizes onto discrete intranuclear domains, the PML-nuclear bodies, and displays anti-oncogenic and pro-apoptotic properties. PLZF encodes a transcription factor belonging to the POZ/domain and Krüppel zinc finger (POK) family which interacts directly with PML. PLZF is related to another POK protein, LAZ3(BCL6), which is structurally altered, and presumably misexpressed, in many non-Hodgkin lymphoma (NHL) cases. PLZF and LAZ3 share many functional properties: both inhibit cell growth, concentrate into punctated nuclear subdomains and are sequence-specific transcriptional repressors recruiting a histone deacetylase-repressing complex. Given these similarities, we tested whether both proteins could be targeted by each other. Here, LAZ3 and PLZF are shown to colocalize onto nuclear dots. Moreover, truncated derivatives of one protein, which display a diffuse nuclear localization, are recruited onto nuclear dots by the full-length other. The colocalization and the reciprocal 'rescue' is the result of a direct interaction between LAZ3 and PLZF, as indicated by yeast two hybrid assays, in vitro immunoprecipitations, and GST pull down experiments. In contrast to LAZ3 homomerization, LAZ3/PLZF heteromerization in yeast does not solely depend on POZ/POZ contacts but rather also relies on interactions between the two zinc finger regions and 'cross' contacts between the zinc finger region and the POZ domain of each partner. Likewise, LAZ3 shows some colocalization with the PLZF partner PML upon stable overexpression of both proteins in CHO cells and interacts with PML in yeast. Finally, endogenous LAZ3 and PLZF are co-induced and partially colocalized in myeloid MDS cells. These data indicate that a physical interaction between LAZ3 and PLZF underlies their simultaneous recruitment onto multiproteic nuclear complexes, presumably involved in transcriptional silencing and whose integrity (for APL) and/or function (for APL and NHL) may be altered in oncogenesis.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/BCL6 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Kruppel-Like Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/Macromolecular Substances, http://linkedlifedata.com/resource/pubmed/chemical/Neoplasm Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Oncogene Proteins, http://linkedlifedata.com/resource/pubmed/chemical/PML protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/Tumor Suppressor Proteins, http://linkedlifedata.com/resource/pubmed/chemical/ZBTB16 protein, human
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0950-9232
pubmed:author
pubmed:issnType
Print
pubmed:day
14
pubmed:volume
19
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
6240-50
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:11175338-Animals, pubmed-meshheading:11175338-CHO Cells, pubmed-meshheading:11175338-COS Cells, pubmed-meshheading:11175338-Cricetinae, pubmed-meshheading:11175338-DNA-Binding Proteins, pubmed-meshheading:11175338-Fluorescent Antibody Technique, pubmed-meshheading:11175338-Humans, pubmed-meshheading:11175338-Kruppel-Like Transcription Factors, pubmed-meshheading:11175338-Leukemia, Promyelocytic, Acute, pubmed-meshheading:11175338-Lymphoma, Non-Hodgkin, pubmed-meshheading:11175338-Macromolecular Substances, pubmed-meshheading:11175338-Neoplasm Proteins, pubmed-meshheading:11175338-Nuclear Proteins, pubmed-meshheading:11175338-Oncogene Proteins, pubmed-meshheading:11175338-Sequence Deletion, pubmed-meshheading:11175338-Transcription Factors, pubmed-meshheading:11175338-Transfection, pubmed-meshheading:11175338-Tumor Cells, Cultured, pubmed-meshheading:11175338-Tumor Suppressor Proteins, pubmed-meshheading:11175338-Two-Hybrid System Techniques, pubmed-meshheading:11175338-Zinc Fingers
pubmed:year
2000
pubmed:articleTitle
Colocalization and heteromerization between the two human oncogene POZ/zinc finger proteins, LAZ3 (BCL6) and PLZF.
pubmed:affiliation
INSERM U524, IRCL, Place de Verdun, 59045 Lille, France.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't