Abstract
The cJun N-terminal kinase (JNK) signal transduction pathway is implicated in the regulation of neuronal function. JNK is encoded by three genes that play partially redundant roles. Here we report the creation of mice with targeted ablation of all three Jnk genes in neurons. Compound JNK-deficient neurons are dependent on autophagy for survival. This autophagic response is caused by FoxO-induced expression of Bnip3 that displaces the autophagic effector Beclin-1 from inactive Bcl-XL complexes. These data identify JNK as a potent negative regulator of FoxO-dependent autophagy in neurons.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Apoptosis / genetics
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Apoptosis / physiology
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Apoptosis Regulatory Proteins / genetics
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Apoptosis Regulatory Proteins / metabolism
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Apoptosis Regulatory Proteins / physiology
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Autophagy / genetics*
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Autophagy / physiology
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Beclin-1
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Cells, Cultured
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Forkhead Box Protein O1
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Forkhead Transcription Factors / genetics
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Forkhead Transcription Factors / metabolism
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Forkhead Transcription Factors / physiology*
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JNK Mitogen-Activated Protein Kinases / genetics
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JNK Mitogen-Activated Protein Kinases / metabolism
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JNK Mitogen-Activated Protein Kinases / physiology*
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Membrane Proteins / genetics
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Membrane Proteins / metabolism
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Membrane Proteins / physiology
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Mice
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Mice, Inbred C57BL
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Mice, Knockout
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Mitochondrial Proteins / genetics
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Mitochondrial Proteins / metabolism
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Mitochondrial Proteins / physiology
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Neurons / metabolism
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Neurons / pathology
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Neurons / physiology*
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Signal Transduction / genetics
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Signal Transduction / physiology
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Transcription Factors / genetics
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Transcription Factors / metabolism
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Transcription Factors / physiology
Substances
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Apoptosis Regulatory Proteins
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BNip3 protein, mouse
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Beclin-1
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Becn1 protein, mouse
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Crtc1 protein, mouse
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Forkhead Box Protein O1
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Forkhead Transcription Factors
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Foxo1 protein, mouse
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Membrane Proteins
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Mitochondrial Proteins
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Transcription Factors
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JNK Mitogen-Activated Protein Kinases