Abstract
Mitogen-activated protein kinases (MAPKs), including p38 and c-Jun N-terminal kinase (JNK), have a key role in T cell receptor (TCR)-induced gene transcription but their precise mechanism of activation is not well understood. The findings of two recent papers provide new insight into the activation of p38 and JNK by the membrane-associated guanylate kinase (MAGUK) family members Dlgh1 and Carma1, respectively, and show how distinct MAGUK proteins control specific aspects of TCR-mediated MAPK activation.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adaptor Proteins, Signal Transducing / metabolism*
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Animals
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Apoptosis Regulatory Proteins / metabolism*
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CARD Signaling Adaptor Proteins / metabolism*
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Cell Line
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Discs Large Homolog 1 Protein
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Enzyme Activation
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Guanylate Kinases
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Humans
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MAP Kinase Kinase 4 / metabolism
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Membrane Proteins / metabolism*
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Mice
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Mitogen-Activated Protein Kinases / metabolism*
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Receptors, Antigen, T-Cell / metabolism*
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Signal Transduction*
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T-Lymphocytes / immunology
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p38 Mitogen-Activated Protein Kinases / metabolism
Substances
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Adaptor Proteins, Signal Transducing
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Apoptosis Regulatory Proteins
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CARD Signaling Adaptor Proteins
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Card11 protein, mouse
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Discs Large Homolog 1 Protein
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Dlg1 protein, mouse
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Membrane Proteins
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Receptors, Antigen, T-Cell
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Mitogen-Activated Protein Kinases
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p38 Mitogen-Activated Protein Kinases
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MAP Kinase Kinase 4
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Guanylate Kinases