Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6775
pubmed:dateCreated
2000-4-12
pubmed:databankReference
pubmed:abstractText
Membrane-associated guanylate kinases (MAGUKs) contain multiple protein-binding domains that allow them to assemble specific multiprotein complexes in particular regions of the cell. CASK/LIN-2, a MAGUK required for EGF receptor localization and signalling in Caenorhabditis elegans, contains a calmodulin-dependent protein kinase-like domain followed by PDZ, SH3 and guanylate kinase-like domains. In adult rat brain, CASK is concentrated at neuronal synapses and binds to the cell-surface proteins neurexin and syndecan and the cytoplasmic proteins Mint/LIN-10 and Veli/LIN-7. Here we report that, through its guanylate kinase domain, CASK interacts with Tbr-1, a T-box transcription factor that is involved in forebrain development. CASK enters the nucleus and binds to a specific DNA sequence (the T-element) in a complex with Tbr-1. CASK acts as a coactivator of Tbr-1 to induce transcription of T-element containing genes, including reelin, a gene that is essential for cerebrocortical development. Our findings show that a MAGUK which is usually associated with cell junctions has a transcription regulation function.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/CASK kinases, http://linkedlifedata.com/resource/pubmed/chemical/Calcium-Calmodulin-Dependent..., http://linkedlifedata.com/resource/pubmed/chemical/Cell Adhesion Molecules, Neuronal, http://linkedlifedata.com/resource/pubmed/chemical/DNA, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Extracellular Matrix Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Guanylate Kinase, http://linkedlifedata.com/resource/pubmed/chemical/Helminth Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Lin-2 protein, C elegans, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Nerve Tissue Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Nucleoside-Phosphate Kinase, http://linkedlifedata.com/resource/pubmed/chemical/Serine Endopeptidases, http://linkedlifedata.com/resource/pubmed/chemical/Tbr1 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/reelin protein
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0028-0836
pubmed:author
pubmed:issnType
Print
pubmed:day
16
pubmed:volume
404
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
298-302
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:10749215-Animals, pubmed-meshheading:10749215-Binding Sites, pubmed-meshheading:10749215-Biological Transport, pubmed-meshheading:10749215-COS Cells, pubmed-meshheading:10749215-Caenorhabditis elegans, pubmed-meshheading:10749215-Calcium-Calmodulin-Dependent Protein Kinases, pubmed-meshheading:10749215-Cell Adhesion Molecules, Neuronal, pubmed-meshheading:10749215-Cell Nucleus, pubmed-meshheading:10749215-Cells, Cultured, pubmed-meshheading:10749215-Cerebral Cortex, pubmed-meshheading:10749215-DNA, pubmed-meshheading:10749215-DNA-Binding Proteins, pubmed-meshheading:10749215-Extracellular Matrix Proteins, pubmed-meshheading:10749215-Gene Expression Regulation, pubmed-meshheading:10749215-Genes, Reporter, pubmed-meshheading:10749215-Guanylate Kinase, pubmed-meshheading:10749215-Helminth Proteins, pubmed-meshheading:10749215-Hippocampus, pubmed-meshheading:10749215-Membrane Proteins, pubmed-meshheading:10749215-Mice, pubmed-meshheading:10749215-Molecular Sequence Data, pubmed-meshheading:10749215-Nerve Tissue Proteins, pubmed-meshheading:10749215-Neurons, pubmed-meshheading:10749215-Nucleoside-Phosphate Kinase, pubmed-meshheading:10749215-Protein Binding, pubmed-meshheading:10749215-Rats, pubmed-meshheading:10749215-Regulatory Sequences, Nucleic Acid, pubmed-meshheading:10749215-Serine Endopeptidases, pubmed-meshheading:10749215-Transcription, Genetic, pubmed-meshheading:10749215-Transcription Factors
pubmed:year
2000
pubmed:articleTitle
Nuclear translocation and transcription regulation by the membrane-associated guanylate kinase CASK/LIN-2.
pubmed:affiliation
Howard Hughes Medical Institute and Department of Neurobiology, Massachusetts General Hospital and Harvard Medical School, Boston 02114, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't