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CASP6 — Caspase-6
CASP6 — Caspase-6
<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">CASP6 — Caspase-6</th>
</tr>
<tr> [@bhatt2012]
<td class="label">Symbol</td> [@bhatt2019]
<td><strong>CASP6</strong></td> [@wong2012]
</tr> [@bhatt2022]
<tr>
<td class="label">Full Name</td>
<td>Caspase-6, Apoptosis-Related Cysteine Peptidase</td>
</tr>
<tr>
<td class="label">Chromosome</td>
<td>4q25</td>
</tr>
<tr>
<td class="label">NCBI Gene</td>
<td><a href="https://www.ncbi.nlm.nih.gov/gene/839" target="_blank">839</a></td>
</tr>
<tr>
<td class="label">Ensembl</td>
<td><a href="https://ensembl.org/Homo_sapiens/Gene/Summary?g=ENSG00000138794" target="_blank">ENSG00000138794</a></td>
</tr>
<tr>
<td class="label">OMIM</td>
<td><a href="https://omim.org/entry/601532" target="_blank">601532</a></td>
</tr>
<tr>
<td class="label">UniProt</td>
<td><a href="https://www.uniprot.org/uniprot/P55212" target="_blank">P55212</a></td>
</tr>
<tr>
<td class="label">Diseases</td>
<td>[Alzheimer's Disease](/diseases/alzheimers), [Huntington's Disease](/diseases/huntingtons), [ALS](/diseases/als)</td>
</tr>
<tr>
<td class="label">Expression</td>
<td>Brain (hippocampus, [cortex](/brain-regions/cortex), striatum), ubiquitous</td>
</tr>
<tr>
<th class="infobox-subheader" colspan="2">Key Substrates</th>
</tr>
<tr>
<td colspan="2" style="font-size:0.85em">[Tau](/proteins/tau) (D421)<br>[Huntingtin](/proteins/huntingtin) (D586)<br>Lamin A/C<br>[APP](/entities/app-protei
CASP6 — Caspase-6
<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">CASP6 — Caspase-6</th>
</tr>
<tr> [@bhatt2012]
<td class="label">Symbol</td> [@bhatt2019]
<td><strong>CASP6</strong></td> [@wong2012]
</tr> [@bhatt2022]
<tr>
<td class="label">Full Name</td>
<td>Caspase-6, Apoptosis-Related Cysteine Peptidase</td>
</tr>
<tr>
<td class="label">Chromosome</td>
<td>4q25</td>
</tr>
<tr>
<td class="label">NCBI Gene</td>
<td><a href="https://www.ncbi.nlm.nih.gov/gene/839" target="_blank">839</a></td>
</tr>
<tr>
<td class="label">Ensembl</td>
<td><a href="https://ensembl.org/Homo_sapiens/Gene/Summary?g=ENSG00000138794" target="_blank">ENSG00000138794</a></td>
</tr>
<tr>
<td class="label">OMIM</td>
<td><a href="https://omim.org/entry/601532" target="_blank">601532</a></td>
</tr>
<tr>
<td class="label">UniProt</td>
<td><a href="https://www.uniprot.org/uniprot/P55212" target="_blank">P55212</a></td>
</tr>
<tr>
<td class="label">Diseases</td>
<td>[Alzheimer's Disease](/diseases/alzheimers), [Huntington's Disease](/diseases/huntingtons), [ALS](/diseases/als)</td>
</tr>
<tr>
<td class="label">Expression</td>
<td>Brain (hippocampus, [cortex](/brain-regions/cortex), striatum), ubiquitous</td>
</tr>
<tr>
<th class="infobox-subheader" colspan="2">Key Substrates</th>
</tr>
<tr>
<td colspan="2" style="font-size:0.85em">[Tau](/proteins/tau) (D421)<br>[Huntingtin](/proteins/huntingtin) (D586)<br>Lamin A/C<br>[APP](/entities/app-protein)<br>α-Tubulin</td>
</tr>
<tr>
<td class="label">Associated Diseases</td>
<td><a href="/wiki/als" style="color:#ef9a9a">Als</a>, <a href="/wiki/alzheimer-disease" style="color:#ef9a9a">Alzheimer Disease</a>, <a href="/wiki/cancer" style="color:#ef9a9a">Cancer</a>, <a href="/wiki/huntington-disease" style="color:#ef9a9a">Huntington Disease</a>, <a href="/wiki/ms" style="color:#ef9a9a">Ms</a></td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">24 edges</a></td>
</tr>
</table>
CASP6 — Caspase-6
Overview
CASP6 (Caspase-6) is a gene on chromosome 4q25 encoding an executioner cysteine-aspartate protease that plays a central role in neuronal [apoptosis](/entities/apoptosis) and neurodegeneration. Unlike other executioner caspases ([CASP3](/genes/casp3), CASP7), caspase-6 has emerged as a uniquely neurodegeneration-relevant protease due to its ability to cleave critical neuronal substrates — most notably [tau](/proteins/tau) at Asp421 and [huntingtin](/proteins/huntingtin-protein) at Asp586 — and its early activation in [Alzheimer's disease](/diseases/alzheimers-disease) and [Huntington's disease](/diseases/huntingtons) pathogenesis.
> Key takeaway: Caspase-6 is the principal protease that cleaves tau at D421 in AD brains and huntingtin at D586 in HD brains. Its activation precedes overt neurodegeneration and is being pursued as a therapeutic target for multiple neurodegenerative diseases.
Gene Structure and Expression
Genomic Organization
CASP6 spans approximately 15 kb on chromosome 4q25, comprising 7 exons. The gene encodes a 293-amino acid proenzyme (procaspase-6) that requires proteolytic activation. Alternative splicing generates CASP6α (full-length, catalytically active) and CASP6β (lacking exon 6, catalytically inactive, acts as dominant-negative inhibitor).
Brain Expression Pattern
CASP6 is expressed broadly in the CNS with particular relevance in:
- [Hippocampus](/brain-regions/hippocampus): Strong expression in CA1 pyramidal [neurons](/entities/neurons), the most vulnerable neurons in AD
- [Entorhinal cortex](/brain-regions/entorhinal-cortex): Activated caspase-6 is detected in the earliest Braak stages (I-II)
- [Striatum](/brain-regions/striatum): High expression in medium spiny neurons, relevant to Huntington's disease
- Cerebral cortex: Broad expression across cortical layers
- [Substantia nigra](/brain-regions/substantia-nigra): Moderate expression in dopaminergic neurons
Expression data is available from the [Allen Human Brain Atlas](https://human.brain-map.org/microarray/search/show?search_term=CASP6).
Transcriptional Regulation
CASP6 expression is regulated by:
- [p53](/entities/tp53): DNA damage and cellular stress upregulate CASP6 transcription
- [NF-κB](/genes/nfkb1): Inflammatory signaling can induce CASP6 expression
- Nerve growth factor deprivation: NGF withdrawal in sympathetic neurons upregulates CASP6
- [Amyloid-β](/proteins/amyloid-beta-protein) exposure: [Aβ](/proteins/amyloid-beta) oligomers increase CASP6 expression and activation in neurons
Function
Activation Mechanism
Procaspase-6 (p34) is activated by proteolytic cleavage:
Neurodegeneration-Relevant Substrates
Caspase-6 cleaves multiple substrates critical for neuronal function:
Non-Apoptotic Functions
Emerging evidence suggests caspase-6 has non-apoptotic roles in neurons:
- Axon pruning: Caspase-6 mediates developmental axon degeneration without triggering neuronal death
- Synaptic plasticity: Low-level caspase-6 activity modulates long-term depression (LTD)
- Neuroinflammation: Caspase-6 activates the [NLRP3](/genes/nlrp3) inflammasome pathway
- B cell activation: Role in adaptive immunity
Disease Associations
Alzheimer's Disease
Caspase-6 plays a central and early role in [AD](/diseases/alzheimers-disease):
- Early activation: Active caspase-6 immunoreactivity is detected in entorhinal cortex and hippocampus at Braak stages I-II, before clinical symptoms appear
- Tau cleavage: Caspase-6-cleaved tau (Tau-ΔC) is a major component of neurofibrillary tangles
- Neoepitope marker: Antibodies recognizing caspase-6-cleaved tau (TauC6) specifically label AD pathology
- Cognitive correlation: Levels of active caspase-6 in hippocampus correlate inversely with episodic and semantic memory performance in non-demented elderly
- Seeding enhancement: Caspase-6-cleaved tau has enhanced aggregation kinetics and promotes [tau seeding](/mechanisms/tau-propagation)
- APP cleavage: Caspase-6 generates toxic C31 fragment of APP, contributing to synaptic dysfunction
Huntington's Disease
Caspase-6 is essential for [HD](/diseases/huntingtons) pathogenesis:
- Cleavage of mutant [huntingtin](/proteins/huntingtin-protein) at Asp586 generates toxic N-terminal fragments
- Huntingtin resistant to caspase-6 cleavage (D586A mutation) prevents neurodegeneration in YAC128 HD mice
- Active caspase-6 is elevated in HD striatum before symptom onset
- Caspase-6 inhibition is neuroprotective in multiple HD models
ALS
In [amyotrophic lateral sclerosis](/diseases/als):
- Caspase-6 is activated in spinal cord motor neurons
- Cleaves [neurofilament](/proteins/neurofilament-light-protein) proteins, contributing to axonal degeneration
- Activated in response to mutant [SOD1](/entities/sod1) toxicity
Ischemic Stroke
- Caspase-6 is rapidly activated after cerebral ischemia
- Contributes to delayed neuronal death in the penumbra
- Inhibition reduces infarct volume in animal models
Expression
Age-Related Changes
| Age Group | Caspase-6 Activity | Significance |
|---|---|---|
| Young adult | Low, basal | Normal neuronal maintenance |
| Middle-aged | Increasing | Begins in entorhinal cortex |
| Elderly (cognitively normal) | Moderate | Correlates with subclinical cognitive decline |
| Mild AD | High | Spreads to hippocampus CA1 |
| Moderate-severe AD | Very high | Widespread cortical activation |
Braak Stage Correlation
Active caspase-6 immunoreactivity closely follows [Braak staging](/mechanisms/braak-staging):
- Stage I-II: Entorhinal cortex (transentorhinal region)
- Stage III-IV: Hippocampus, temporal cortex
- Stage V-VI: Neocortical regions
This distribution parallels [tau pathology](/mechanisms/tau-propagation) spread and precedes frank neuronal loss.
Therapeutic Targeting
Caspase-6 Inhibitors
- Z-VEID-FMK: Research tool peptidomimetic inhibitor; neuroprotective in cell and animal models
- Peptide-based inhibitors: VEID tetrapeptide derivatives with improved selectivity
- Small molecule inhibitors: Multiple pharmaceutical programs targeting caspase-6 active site
- Allosteric inhibitors: Compounds binding outside the active site to lock caspase-6 in an inactive conformation
- Zinc coordination: Zinc inhibits caspase-6 at physiological concentrations, suggesting metal homeostasis as a regulatory mechanism
Alternative Approaches
- Upstream intervention: Blocking caspase-6 activation by inhibiting caspase-1 or caspase-3
- Substrate protection: Designing tau or huntingtin mutants resistant to caspase-6 cleavage (gene therapy approaches)
- Dominant-negative CASP6β: Overexpression of the inactive splice variant to compete with active caspase-6
- Anti-sense oligonucleotides: Reducing CASP6 expression
See Also
- [CASP3](/genes/casp3) — Related executioner caspase
- [CASP1](/genes/casp1) — Upstream activating caspase
- [Tau Protein](/proteins/tau) — Critical substrate
- [Huntingtin](/proteins/huntingtin-protein) — HD-relevant substrate
- [Apoptosis](/mechanisms/apoptosis) — Cell death pathway
- [Neurofibrillary Tangles](/mechanisms/neurofibrillary-tangles) — Downstream pathology
External Links
- [CASP6 at NCBI Gene](https://www.ncbi.nlm.nih.gov/gene/839)
- [CASP6 at UniProt (P55212)](https://www.uniprot.org/uniprot/P55212)
- [CASP6 at OMIM (601532)](https://omim.org/entry/601532)
- [CASP6 at GeneCards](https://www.genecards.org/cgi-bin/carddisp.pl?gene=CASP6)
- [Allen Brain Atlas — CASP6](https://human.brain-map.org/microarray/search/show?search_term=CASP6)
References
Pathway Diagram
The following diagram shows the key molecular relationships involving CASP6 — Caspase-6 discovered through SciDEX knowledge graph analysis:
▸Metadataorigin_type: v1_polymorphic_backfill
| slug | genes-casp6 |
| kg_node_id | CASP6 |
| entity_type | gene |
| origin_type | v1_polymorphic_backfill |
| source_table | wiki_pages |
| wiki_page_id | wp-21557a137ea8 |
| __merged_from | {'merged_at': '2026-05-13', 'unprefixed_id': 'genes-casp6'} |
| _schema_version | 1 |
No provenance edges found
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[CASP6 — Caspase-6](http://scidex.ai/artifact/wiki-genes-casp6)
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