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Journal of Biological Chemistry
Article . 2002 . Peer-reviewed
License: CC BY
Data sources: Crossref
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Journal of Biological Chemistry
Article
License: CC BY
Data sources: UnpayWall
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The p75 Neurotrophin Receptor Interacts with Multiple MAGE Proteins

Authors: Marianna, Tcherpakov; Francisca C, Bronfman; Silvestro G, Conticello; Anna, Vaskovsky; Zehava, Levy; Michio, Niinobe; Kazuaki, Yoshikawa; +2 Authors

The p75 Neurotrophin Receptor Interacts with Multiple MAGE Proteins

Abstract

The p75 neurotrophin receptor has been implicated in diverse aspects of neurotrophin signaling, but the mechanisms by which its effects are mediated are not well understood. Here we identify two MAGE proteins, necdin and MAGE-H1, as interactors for the intracellular domain of p75 and show that the interaction is enhanced by ligand stimulation. PC12 cells transfected with necdin or MAGE-H1 exhibit accelerated differentiation in response to nerve growth factor. Expression of these two MAGE proteins is predominantly cytoplasmic in PC12 cells, and necdin was found to be capable of homodimerization, suggesting that it may act as a cytoplasmic adaptor to recruit a signaling complex to p75. These findings indicate that diverse MAGE family members can interact with the p75 receptor and highlight type II MAGE proteins as a potential family of interactors for signaling proteins containing type II death domains.

Country
Chile
Keywords

Cytoplasm, DNA, Complementary, Cerebro, Blotting, Western, 610, Nerve Tissue Proteins, Neuronas, PC12 Cells, Proteinas, Mice, Animals, Cloning, Molecular, Phylogeny, Gene Library, Nuclear Proteins, Precipitin Tests, Neoplasm Proteins, Protein Structure, Tertiary, Rats, Microscopy, Fluorescence, COS Cells, Medicina y salud, Microtubule-Associated Proteins, Plasmids, Protein Binding

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    selected citations
    These citations are derived from selected sources.
    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    82
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 10%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Top 10%
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 10%
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
82
Top 10%
Top 10%
Top 10%
gold