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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
32
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pubmed:dateCreated |
2004-8-2
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pubmed:abstractText |
The cytoplasmic adaptor protein Disabled-1 (Dab1) is necessary for the regulation of neuronal positioning in the developing brain by the secreted molecule Reelin. Binding of Reelin to the neuronal apolipoprotein E receptors apoER2 and very low density lipoprotein receptor induces tyrosine phosphorylation of Dab1 and the subsequent activation or relocalization of downstream targets like phosphatidylinositol 3 (PI3)-kinase and Nckbeta. Disruption of Reelin signaling leads to the accumulation of Dab1 protein in the brains of genetically modified mice, suggesting that Reelin limits its own action in responsive neurons by down-regulating the levels of Dab1 expression. Here, we use cultured primary embryonic neurons as a model to demonstrate that Reelin treatment targets Dab1 for proteolytic degradation by the ubiquitin-proteasome pathway. We show that tyrosine phosphorylation of Dab1 but not PI3-kinase activation is required for its proteasomal targeting. Genetic deficiency in the Dab1 kinase Fyn prevents Dab1 degradation. The Reelin-induced Dab1 degradation also depends on apoER2 and very low density lipoprotein receptor in a gene-dose dependent manner. Moreover, pharmacological blockade of the proteasome prevents the formation of a proper cortical plate in an in vitro slice culture assay. Our results demonstrate that signaling through neuronal apoE receptors can activate the ubiquitin-proteasome machinery, which might have implications for the role of Reelin during neurodevelopment and in the regulation of synaptic transmission.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Cell Adhesion Molecules, Neuronal,
http://linkedlifedata.com/resource/pubmed/chemical/Cysteine Endopeptidases,
http://linkedlifedata.com/resource/pubmed/chemical/Dab1 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Enzyme Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Extracellular Matrix Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/FYN protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Fyn protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Fyn protein, rat,
http://linkedlifedata.com/resource/pubmed/chemical/Low Density Lipoprotein...,
http://linkedlifedata.com/resource/pubmed/chemical/Multienzyme Complexes,
http://linkedlifedata.com/resource/pubmed/chemical/Nerve Tissue Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphatidylinositol 3-Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/Proteasome Endopeptidase Complex,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-fyn,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, LDL,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Fusion Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Serine Endopeptidases,
http://linkedlifedata.com/resource/pubmed/chemical/Tyrosine,
http://linkedlifedata.com/resource/pubmed/chemical/Ubiquitin,
http://linkedlifedata.com/resource/pubmed/chemical/VLDL receptor,
http://linkedlifedata.com/resource/pubmed/chemical/reelin protein,
http://linkedlifedata.com/resource/pubmed/chemical/src-Family Kinases
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0021-9258
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
6
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pubmed:volume |
279
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
33471-9
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:15175346-Amino Acid Sequence,
pubmed-meshheading:15175346-Animals,
pubmed-meshheading:15175346-Binding Sites,
pubmed-meshheading:15175346-Cell Adhesion Molecules, Neuronal,
pubmed-meshheading:15175346-Cells, Cultured,
pubmed-meshheading:15175346-Cerebral Cortex,
pubmed-meshheading:15175346-Culture Techniques,
pubmed-meshheading:15175346-Cysteine Endopeptidases,
pubmed-meshheading:15175346-Embryo, Mammalian,
pubmed-meshheading:15175346-Enzyme Inhibitors,
pubmed-meshheading:15175346-Extracellular Matrix Proteins,
pubmed-meshheading:15175346-Humans,
pubmed-meshheading:15175346-Immunohistochemistry,
pubmed-meshheading:15175346-Low Density Lipoprotein Receptor-Related Protein-1,
pubmed-meshheading:15175346-Mice,
pubmed-meshheading:15175346-Mice, Inbred C57BL,
pubmed-meshheading:15175346-Molecular Sequence Data,
pubmed-meshheading:15175346-Multienzyme Complexes,
pubmed-meshheading:15175346-Mutation,
pubmed-meshheading:15175346-Nerve Tissue Proteins,
pubmed-meshheading:15175346-Neurons,
pubmed-meshheading:15175346-Phosphatidylinositol 3-Kinases,
pubmed-meshheading:15175346-Phosphorylation,
pubmed-meshheading:15175346-Polymerase Chain Reaction,
pubmed-meshheading:15175346-Proteasome Endopeptidase Complex,
pubmed-meshheading:15175346-Proto-Oncogene Proteins,
pubmed-meshheading:15175346-Proto-Oncogene Proteins c-fyn,
pubmed-meshheading:15175346-RNA, Messenger,
pubmed-meshheading:15175346-Rats,
pubmed-meshheading:15175346-Rats, Sprague-Dawley,
pubmed-meshheading:15175346-Receptors, LDL,
pubmed-meshheading:15175346-Recombinant Fusion Proteins,
pubmed-meshheading:15175346-Serine Endopeptidases,
pubmed-meshheading:15175346-Signal Transduction,
pubmed-meshheading:15175346-Transfection,
pubmed-meshheading:15175346-Tyrosine,
pubmed-meshheading:15175346-Ubiquitin,
pubmed-meshheading:15175346-src-Family Kinases
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pubmed:year |
2004
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pubmed:articleTitle |
Apolipoprotein E receptors are required for reelin-induced proteasomal degradation of the neuronal adaptor protein Disabled-1.
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pubmed:affiliation |
Department of Medicine II, Albert-Ludwigs-Universität, Albertstrasse 23, 79104 Freiburg, Germany. hans.bock@zfn.uni-freiburg.de
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pubmed:publicationType |
Journal Article
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