Abstract
Disruption of the adaptor protein ELF, a beta-spectrin, leads to disruption of transforming growth factor-beta (TGF-beta) signaling by Smad proteins in mice. Elf-/- mice exhibit a phenotype similar to smad2+/-/smad3+/- mutant mice of midgestational death due to gastrointestinal, liver, neural, and heart defects. We show that TGF-beta triggers phosphorylation and association of ELF with Smad3 and Smad4, followed by nuclear translocation. ELF deficiency results in mislocalization of Smad3 and Smad4 and loss of the TGF-beta-dependent transcriptional response, which could be rescued by overexpression of the COOH-terminal region of ELF. This study reveals an unexpected molecular link between a major dynamic scaffolding protein and a key signaling pathway.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Abnormalities, Multiple
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Animals
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Carrier Proteins / metabolism
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Cell Membrane / metabolism
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Cell Nucleus / metabolism
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Contractile Proteins / metabolism
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DNA-Binding Proteins / metabolism
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Embryonic and Fetal Development
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Filamins
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Gene Targeting
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Genes, fos
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Liver / abnormalities
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Liver / embryology
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Liver / metabolism*
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Mice
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Mice, Knockout
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Microfilament Proteins / metabolism
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Microscopy, Confocal
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Mutation
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Phenotype
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Phosphorylation
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Platelet-Derived Growth Factor / pharmacology
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Signal Transduction*
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Smad2 Protein
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Smad3 Protein
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Smad4 Protein
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Spectrin / genetics
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Spectrin / metabolism*
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Trans-Activators / metabolism
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Transcriptional Activation
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Transforming Growth Factor beta / metabolism*
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Transforming Growth Factor beta / pharmacology
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Tumor Cells, Cultured
Substances
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Carrier Proteins
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Contractile Proteins
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DNA-Binding Proteins
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Filamins
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Microfilament Proteins
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Platelet-Derived Growth Factor
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Smad2 Protein
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Smad2 protein, mouse
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Smad3 Protein
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Smad3 protein, mouse
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Smad4 Protein
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Smad4 protein, mouse
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Trans-Activators
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Transforming Growth Factor beta
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Spectrin