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PMID: 10749215 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Nuclear translocation and transcription regulation by the membrane-associated guanylate kinase CASK/LIN-2.

Nature ·Vol. 404 ·No. 6775 ·2000-03-16 ·Pages 298-302

Hsueh YP, Wang TF, Yang FC, Sheng M

Abstract

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.

MeSH Terms
Animals Binding Sites Biological Transport COS Cells Caenorhabditis elegans Calcium-Calmodulin-Dependent Protein Kinases Cell Adhesion Molecules, Neuronal/metabolism Cell Nucleus/metabolism Cells, Cultured Cerebral Cortex/embryology,physiology DNA/metabolism DNA-Binding Proteins/metabolism Extracellular Matrix Proteins/metabolism Gene Expression Regulation Genes, Reporter Guanylate Kinases Helminth Proteins/metabolism Hippocampus/cytology Membrane Proteins/metabolism Mice Molecular Sequence Data Nerve Tissue Proteins Neurons/metabolism Nucleoside-Phosphate Kinase/metabolism Protein Binding Rats Reelin Protein Regulatory Sequences, Nucleic Acid Serine Endopeptidases T-Box Domain Proteins Transcription Factors/physiology Transcription, Genetic
Chemicals
Cell Adhesion Molecules, Neuronal DNA-Binding Proteins Extracellular Matrix Proteins Helminth Proteins Lin-2 protein, C elegans Membrane Proteins Nerve Tissue Proteins Reelin Protein Reln protein, rat T-Box Domain Proteins Tbr1 protein, mouse Transcription Factors DNA CASK kinases Calcium-Calmodulin-Dependent Protein Kinases Nucleoside-Phosphate Kinase Guanylate Kinases Reln protein, mouse Serine Endopeptidases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Hsueh Y P
Howard Hughes Medical Institute and Department of Neurobiology, Massachusetts General Hospital and Harvard Medical School, Boston 02114, USA.
Wang T F
Yang F C
Sheng M
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
2000-03-16
Pages
298-302
Language
English
Region
England
NLM ID
0410462
Subset
IM
Databases
GENBANK
AC002067
Corrections
ErratumIn
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CommentIn
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