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JNK (c-Jun N-terminal Kinase) Protein
JNK (c-Jun N-terminal Kinase) Protein
<table class="infobox infobox-protein">
<tr>
<th class="infobox-header" colspan="2">JNK (c-Jun N-terminal Kinase) Protein</th>
</tr>
<tr>
<td class="label">Gene Symbol</td>
<td>MAPK8 (JNK1), MAPK9 (JNK2), MAPK10 (JNK3)</td>
</tr>
<tr>
<td class="label">Chromosomal Location</td>
<td>MAPK8: 10q11.22, MAPK9: 5q35.1, MAPK10: 4q21.3</td>
</tr>
<tr>
<td class="label">UniProt IDs</td>
<td>P45983 (JNK1), P45984 (JNK2), P53779 (JNK3)</td>
</tr>
<tr>
<td class="label">Molecular Weight</td>
<td>~46-48 kDa per isoform</td>
</tr>
<tr>
<td class="label">Compound</td>
<td>Selectivity</td>
</tr>
<tr>
<td class="label">SP600125</td>
<td>Broad JNK inhibitor</td>
</tr>
<tr>
<td class="label">JNK-IN-8</td>
<td>Selective JNK inhibitor</td>
</tr>
<tr>
<td class="label">CC-401 (CC-930)</td>
<td>JNK inhibitor</td>
</tr>
<tr>
<td class="label">D-JNKI1</td>
<td>Peptide inhibitor</td>
</tr>
<tr>
<td class="label">Partner</td>
<td>Interaction Type</td>
</tr>
<tr>
<td class="label">MKK4</td>
<td>Phosphorylation</td>
</tr>
<tr>
<td class="label">MKK7</td>
<td>Phosphorylation</td>
</tr>
<tr>
<td class="label">c-Jun</td>
<td>Phosphorylation</td>
</tr>
<tr>
<td class="label">Bim (BCL2L11)</td>
<td>Phosphorylation</td>
</tr>
<tr>
<td class="label">Bcl-2</td>
<td>Phosphorylation</td>
</tr>
<tr>
<td class="label">Tau (MAPT)</td>
<td>Phosphorylation</td>
</tr>
<tr>
<td
JNK (c-Jun N-terminal Kinase) Protein
<table class="infobox infobox-protein">
<tr>
<th class="infobox-header" colspan="2">JNK (c-Jun N-terminal Kinase) Protein</th>
</tr>
<tr>
<td class="label">Gene Symbol</td>
<td>MAPK8 (JNK1), MAPK9 (JNK2), MAPK10 (JNK3)</td>
</tr>
<tr>
<td class="label">Chromosomal Location</td>
<td>MAPK8: 10q11.22, MAPK9: 5q35.1, MAPK10: 4q21.3</td>
</tr>
<tr>
<td class="label">UniProt IDs</td>
<td>P45983 (JNK1), P45984 (JNK2), P53779 (JNK3)</td>
</tr>
<tr>
<td class="label">Molecular Weight</td>
<td>~46-48 kDa per isoform</td>
</tr>
<tr>
<td class="label">Compound</td>
<td>Selectivity</td>
</tr>
<tr>
<td class="label">SP600125</td>
<td>Broad JNK inhibitor</td>
</tr>
<tr>
<td class="label">JNK-IN-8</td>
<td>Selective JNK inhibitor</td>
</tr>
<tr>
<td class="label">CC-401 (CC-930)</td>
<td>JNK inhibitor</td>
</tr>
<tr>
<td class="label">D-JNKI1</td>
<td>Peptide inhibitor</td>
</tr>
<tr>
<td class="label">Partner</td>
<td>Interaction Type</td>
</tr>
<tr>
<td class="label">MKK4</td>
<td>Phosphorylation</td>
</tr>
<tr>
<td class="label">MKK7</td>
<td>Phosphorylation</td>
</tr>
<tr>
<td class="label">c-Jun</td>
<td>Phosphorylation</td>
</tr>
<tr>
<td class="label">Bim (BCL2L11)</td>
<td>Phosphorylation</td>
</tr>
<tr>
<td class="label">Bcl-2</td>
<td>Phosphorylation</td>
</tr>
<tr>
<td class="label">Tau (MAPT)</td>
<td>Phosphorylation</td>
</tr>
<tr>
<td class="label">ATF2</td>
<td>Phosphorylation</td>
</tr>
<tr>
<td class="label">p53</td>
<td>Phosphorylation</td>
</tr>
<tr>
<td class="label">Associated Diseases</td>
<td><a href="/wiki/ad" style="color:#ef9a9a">AD</a>, <a href="/wiki/ali" style="color:#ef9a9a">ALI</a>, <a href="/wiki/als" style="color:#ef9a9a">ALS</a>, <a href="/wiki/alzheimer" style="color:#ef9a9a">ALZHEIMER</a>, <a href="/wiki/ami" style="color:#ef9a9a">AMI</a></td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">1286 edges</a></td>
</tr>
</table>
JNK (c-Jun N-terminal kinase, also known as MAPK8) is a stress-activated serine/threonine protein kinase belonging to the MAPK family. It is activated by cellular stress, inflammatory cytokines, and excitotoxicity, playing complex and context-dependent roles in neuronal survival and death. JNK is particularly implicated in [Alzheimer's disease](/diseases/alzheimers-disease), [Parkinson's disease](/diseases/parkinsons-disease), and other neurodegenerative disorders. [@bhujbal2025]
Pathway Diagram
Gene and Isoforms
JNK exists as three isoforms: JNK1 and JNK2 are ubiquitously expressed, while JNK3 is predominantly neuronal and is the major isoform implicated in neurodegeneration. [@moro2023]
Structure
JNK proteins share a central kinase domain flanked by N- and C-terminal regions. The kinase domain adopts a typical bilobal structure characteristic of protein kinases. JNK is activated by dual phosphorylation on a Thr-X-Tyr (TXY) motif within its activation loop, catalyzed by upstream MKK4 and MKK7 kinases. The JNK3 isoform contains a unique 30-amino acid C-terminal extension that may confer neuronal specificity. [@reijnders2020]
Normal Function
Activation Mechanisms
JNK is activated through a canonical three-tier kinase cascade:
Key Targets
- c-Jun: Primary transcription factor substrate; phosphorylation at Ser63/Ser73 promotes AP-1-mediated gene transcription
- Bim (BCL2L11): Pro-apoptotic BH3-only protein; JNK-mediated phosphorylation activates Bim
- BAD: Pro-apoptotic protein; phosphorylation promotes cell death
- [Tau](/proteins/tau): JNK phosphorylates tau at multiple sites including Ser396, Thr181, and Ser202 -- sites also targeted by other stress kinases in Alzheimer's disease [@yoshikawa2023]
- ATF2: Stress-responsive transcription factor
- Bcl-2: JNK can phosphorylate anti-apoptotic Bcl-2, reducing its protective function
Physiological Roles
In the healthy brain, JNK regulates:
- Stress response and cellular adaptation to environmental insults
- Neuronal development and differentiation
- Synaptic plasticity and dendritic spine morphology
- Regulation of neuronal excitability
Role in Alzheimer's Disease
JNK is strongly activated in [Alzheimer's disease](/diseases/alzheimers-disease) brains, particularly in regions vulnerable to neurodegeneration such as the hippocampus and prefrontal cortex. [@manoharan2023]
Neuronal Death Pathways
- c-Jun activation: JNK-mediated phosphorylation of c-Jun promotes expression of pro-apoptotic genes
- Bim activation: JNK phosphorylates Bim, relieving it from inhibition by Bcl-2/Bcl-xL, leading to mitochondrial outer membrane permeabilization (MOMP)
- Caspase activation: JNK contributes to caspase-3 and caspase-9 activation through both intrinsic (mitochondrial) and extrinsic (death receptor) pathways
Tau Pathology
JNK directly phosphorylates [tau](/proteins/tau) at multiple pathological sites. In AD brains, p-JNK colocalizes with neurofibrillary tangles, and JNK activity correlates with Braak staging. JNK also phosphorylates the microtubule-associated protein tau (MAPT) gene promoter, potentially altering tau expression levels. [@yoshikawa2023]
Amyloid-Beta Interactions
[Aβ](/proteins/amyloid-beta) oligomers activate the JNK pathway through multiple mechanisms:
- Aβ binds to various neuronal receptors (e.g., NMDA receptors, RAGE) that trigger upstream kinase activation
- Aβ-induced oxidative stress activates MLK3-MKK4/7-JNK cascade
- JNK activation contributes to Aβ-induced synaptic dysfunction and spine loss
- Inhibition of JNK protects against Aβ-induced neuronal death in cultured neurons and animal models [@manoharan2023]
Role in Parkinson's Disease
JNK3 is the predominant isoform in dopaminergic neurons of the substantia nigra pars compacta and is implicated in [Parkinson's disease](/diseases/parkinsons-disease) through multiple mechanisms. [@kumar2021]
Dopaminergic Neuron Vulnerability
- Mitochondrial dysfunction: JNK is activated by mitochondrial stress and contributes to MPTP/MPTP model dopaminergic toxicity
- α-Synuclein aggregation: [α-synuclein](/proteins/alpha-synuclein) oligomers activate JNK; JNK activation in turn promotes α-synuclein aggregation and spread
- Inflammation: Microglial JNK activation drives production of pro-inflammatory cytokines (IL-1β, TNF-α) that damage dopaminergic neurons
Neuroprotection Studies
- JNK3 knockout mice show reduced dopaminergic neuron death in MPTP models
- Peptide inhibitors of JNK (e.g., D-JNKI1) protect against 6-OHDA and MPTP toxicity
- Small molecule JNK inhibitors (SP600125, JNK-IN-8) reduce neurodegeneration in PD animal models
Role in Other Neurodegenerative Disorders
Huntington's Disease
- Mutant [huntingtin](/proteins/huntingtin) protein activates JNK through aberrant protein interactions and transcriptional dysregulation
- JNK contributes to striatal neuron death through c-Jun activation and mitochondrial dysfunction
- JNK inhibition reduces toxicity in HD models
Amyotrophic Lateral Sclerosis (ALS)
- JNK is activated in motor neurons in ALS models and patient samples
- Both SOD1 and TDP-43 mutations activate the JNK pathway
- JNK inhibition delays disease onset and extends survival in SOD1 mouse models
Stroke and Traumatic Brain Injury
- Ischemia rapidly and strongly activates JNK in affected brain regions
- JNK contributes to both neuronal death and glial activation in stroke
- JNK inhibitors reduce infarct volume when administered within therapeutic windows
Therapeutic Targeting
Small Molecule Inhibitors
Clinical Status
JNK inhibitors have been tested in clinical trials for inflammatory diseases (rheumatoid arthritis, COPD) with acceptable safety profiles, establishing a foundation for neurodegenerative applications. However, JNK inhibitors have not yet reached Phase 2/3 trials for AD or PD. [@bhujbal2025]
Challenges
- Achieving CNS penetration with small molecule JNK inhibitors
- Isoform selectivity (targeting JNK3 over JNK1/2 to reduce peripheral toxicity)
- Timing of intervention -- JNK has both protective and destructive roles depending on context
- Biomarker development for patient selection
Protein Interactions
See Also
- [Alzheimer's Disease](/diseases/alzheimers-disease)
- [Parkinson's Disease](/diseases/parkinsons-disease)
- [Huntington's Disease](/diseases/huntingtons-disease)
- [Tau Protein](/proteins/tau)
- [Apoptosis Pathway](/mechanisms/apoptosis)
- [MAPK Signaling Cascade](/mechanisms/mapk-signaling-pathway)
References
Pathway Diagram
The following diagram shows the key molecular relationships involving JNK (c-Jun N-terminal Kinase) Protein discovered through SciDEX knowledge graph analysis:
▸Metadataorigin_type: v1_polymorphic_backfill
| slug | proteins-jnk |
| kg_node_id | JNK |
| entity_type | protein |
| origin_type | v1_polymorphic_backfill |
| source_table | wiki_pages |
| wiki_page_id | wp-8a140dfbb58a |
| __merged_from | {'merged_at': '2026-05-13', 'unprefixed_id': 'proteins-jnk'} |
| _schema_version | 1 |
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