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SIRT3 - Sirtuin 3
SIRT3 - Sirtuin 3
Overview
<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">SIRT3 - Sirtuin 3</th>
</tr>
<tr>
<td class="label">Gene Symbol</td>
<td>SIRT3</td>
</tr>
<tr>
<td class="label">Full Name</td>
<td>Sirtuin 3</td>
</tr>
<tr>
<td class="label">Chromosomal Location</td>
<td>11p15.5</td>
</tr>
<tr>
<td class="label">NCBI Gene ID</td>
<td>23410</td>
</tr>
<tr>
<td class="label">OMIM</td>
<td>604479</td>
</tr>
<tr>
<td class="label">Ensembl ID</td>
<td>ENSG00000142092</td>
</tr>
<tr>
<td class="label">UniProt</td>
<td>Q9NWU1</td>
</tr>
<tr>
<td class="label">Approach</td>
<td>Status</td>
</tr>
<tr>
<td class="label">SRT1720</td>
<td>Preclinical</td>
</tr>
<tr>
<td class="label">NAD+ precursors (NR, NMN)</td>
<td>Phase 2</td>
</tr>
<tr>
<td class="label">Honokiol</td>
<td>Preclinical</td>
</tr>
<tr>
<td class="label">Gene therapy (AAV-SIRT3)</td>
<td>Research</td>
</tr>
<tr>
<td class="label">Approach</td>
<td>Status</td>
</tr>
<tr>
<td class="label">SIRT3 activators</td>
<td>Preclinical</td>
</tr>
<tr>
<td class="label">NAD+ boosters</td>
<td>Clinical</td>
</tr>
<tr>
<td class="label">Gene therapy</td>
<td>Research</td>
</tr>
<tr>
<td class="label">Associated Diseases</td>
<td><a href="/wiki/als" style="color:#ef9a9a">ALS</a>, <a href="/wiki/alzheimer" style="color:#ef9a9a">ALZHEIMER</a>, <a href="/
SIRT3 - Sirtuin 3
Overview
<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">SIRT3 - Sirtuin 3</th>
</tr>
<tr>
<td class="label">Gene Symbol</td>
<td>SIRT3</td>
</tr>
<tr>
<td class="label">Full Name</td>
<td>Sirtuin 3</td>
</tr>
<tr>
<td class="label">Chromosomal Location</td>
<td>11p15.5</td>
</tr>
<tr>
<td class="label">NCBI Gene ID</td>
<td>23410</td>
</tr>
<tr>
<td class="label">OMIM</td>
<td>604479</td>
</tr>
<tr>
<td class="label">Ensembl ID</td>
<td>ENSG00000142092</td>
</tr>
<tr>
<td class="label">UniProt</td>
<td>Q9NWU1</td>
</tr>
<tr>
<td class="label">Approach</td>
<td>Status</td>
</tr>
<tr>
<td class="label">SRT1720</td>
<td>Preclinical</td>
</tr>
<tr>
<td class="label">NAD+ precursors (NR, NMN)</td>
<td>Phase 2</td>
</tr>
<tr>
<td class="label">Honokiol</td>
<td>Preclinical</td>
</tr>
<tr>
<td class="label">Gene therapy (AAV-SIRT3)</td>
<td>Research</td>
</tr>
<tr>
<td class="label">Approach</td>
<td>Status</td>
</tr>
<tr>
<td class="label">SIRT3 activators</td>
<td>Preclinical</td>
</tr>
<tr>
<td class="label">NAD+ boosters</td>
<td>Clinical</td>
</tr>
<tr>
<td class="label">Gene therapy</td>
<td>Research</td>
</tr>
<tr>
<td class="label">Associated Diseases</td>
<td><a href="/wiki/als" style="color:#ef9a9a">ALS</a>, <a href="/wiki/alzheimer" style="color:#ef9a9a">ALZHEIMER</a>, <a href="/wiki/alzheimer's-disease" style="color:#ef9a9a">ALZHEIMER'S DISEASE</a>, <a href="/wiki/aging" style="color:#ef9a9a">Aging</a>, <a href="/wiki/als" style="color:#ef9a9a">Als</a></td>
</tr>
<tr>
<td class="label">SciDEX Hypotheses</td>
<td><a href="/hypothesis/h-seaad-v4-5a7a4079" style="color:#ce93d8" title="Score: 0.68">SIRT3-Mediated Mitochondrial Deacetylati...</a><br><a href="/hypothesis/h-0e614ae4" style="color:#ce93d8" title="Score: 0.45">Mitochondrial-Nuclear Epigenetic Cross-T...</a></td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">725 edges</a></td>
</tr>
</table>
Sirt3 Sirtuin 3 plays an important role in the study of neurodegenerative diseases. This page provides comprehensive information about this topic, including its mechanisms, significance in disease processes, and therapeutic implications.
Pathway Diagram
Introduction
Sirt3 Sirtuin 3 is an important component in the neurobiology of neurodegenerative diseases. This page provides detailed information about its structure, function, and role in disease processes. [@smad]
SIRT3 is a member of the sirtuin family of NAD+-dependent deacetylases, primarily localized to mitochondria. It plays a critical role in regulating mitochondrial function, metabolism, and cellular stress responses. [@transcriptional]
Gene Overview
Function
SIRT3 is the primary mitochondrial deacetylase, regulating key metabolic enzymes and proteins involved in:
- Mitochondrial protein acetylation: Deacetylates over 20 mitochondrial proteins, including IDH2, SDH, GDH, LCAD, and HSD17B10
- ATP production: Modulates electron transport chain complex activity to optimize oxidative phosphorylation
- [ROS](/entities/reactive-oxygen-species) detoxification: Activates SOD2 (manganese superoxide dismutase) by deacetylation to reduce oxidative stress
- Fatty acid oxidation: Activates LCAD (long-chain acyl-CoA dehydrogenase) to promote fatty acid metabolism
- Ketogenesis: Regulates HMGCS2 to enhance ketone body production during fasting
Disease Associations
Alzheimer's Disease
- SIRT3 expression is reduced in AD brains and AD mouse models
- SIRT3 deacetylates SOD2 to protect [neurons](/entities/neurons) from [Aβ](/proteins/amyloid-beta)-induced oxidative stress
- SIRT3 activation promotes mitochondrial biogenesis and improves Therapeutic potential: SIRT3 activators (e.g., honokiol, cognitive function
- resveratrol derivatives) are being investigated
Parkinson's Disease
SIRT3 is the primary mitochondrial deacetylase and plays a critical protective role in dopaminergic neurons. SIRT3 protects dopaminergic neurons from mitochondrial dysfunction through:
- Complex I protection: SIRT3 deacetylates complex I subunits to maintain electron transport chain function—directly relevant to PD given the well-established complex I deficiency in PD substantia nigra. PMID: 25933439(https://pubmed.ncbi.nlm.nih.gov/25933439/)
- MnSOD activation: SIRT3 deacetylates manganese superoxide dismutase (MnSOD), enhancing its enzymatic activity to reduce oxidative stress in dopaminergic neurons.
- IDH2 activation: SIRT3 deacetylates isocitrate dehydrogenase 2 (IDH2), increasing NADP+/NADPH production crucial for reducing glutathione and combating oxidative stress.
Sirtuin Pathway Dysfunction Hypothesis
The [Sirtuin Pathway Dysfunction Hypothesis in Parkinson's Disease](/hypotheses/sirtuin-pathway-dysfunction-parkinsons) identifies SIRT3 as a key mitochondrial guardian whose dysfunction contributes to PD pathogenesis:
Therapeutic Implications
SIRT3 activation is a promising therapeutic approach for PD:
The [NADAPT Study (NCT06162013)](/clinical-trials/nadapt-study-nad-replenishment-parkinsonism-nct06162013) evaluates NAD+ precursor supplementation that indirectly enhances SIRT3 activity through increased NAD+ substrate.
See the [Sirtuin Pathway Dysfunction Validation Experiment](/experiments/sirtuin-pathway-dysfunction-parkinsons) for detailed study design including SIRT3-targeted interventions.
Amyotrophic Lateral Sclerosis (ALS)
- SIRT3 levels are decreased in ALS models and patient tissues
- Protects motor neurons from mitochondrial dysfunction and oxidative stress
- SIRT3 deacetylase activity is protective in SOD1 and [TDP-43](/proteins/tdp-43) models
Huntington's Disease
- SIRT3 ameliorates mitochondrial dysfunction in HD models
- Protects against mutant [huntingtin](/proteins/huntingtin-protein)-induced metabolic deficits
Expression Pattern
SIRT3 is highly expressed in:
- Brain: [Hippocampus](/brain-regions/hippocampus), cerebral [cortex](/brain-regions/cortex), basal ganglia, cerebellum
- High energy-demand tissues: Heart, liver, kidney, skeletal muscle
- Neuronal subtypes: Particularly enriched in dopaminergic neurons
Therapeutic Targeting
Key Publications
See Also
- [SIRT1 Gene](/genes/sirt1)
- [SIRT2 Gene](/genes/sirt2)
- [Mitochondrial Dysfunction Pathway](/mechanisms/mitochondrial-dysfunction-pathway)
- [Oxidative Stress Pathway](/mechanisms/oxidative-stress-pathway)
- [Sirtuin Modulators Treatment](/therapeutics/sirtuin-modulators)
- [Sirtuin Pathway Dysfunction Hypothesis in PD](/hypotheses/sirtuin-pathway-dysfunction-parkinsons)
- [Sirtuin Pathway Dysfunction Validation Experiment](/experiments/sirtuin-pathway-dysfunction-parkinsons)
External Links
- [NCBI Gene: SIRT3](https://www.ncbi.nlm.nih.gov/gene/23410)
- [UniProt: SIRT3](https://www.uniprot.org/uniprot/Q9NWU1)
- [OMIM: SIRT3](https://www.omim.org/entry/604479)
- [Allen Brain Atlas: SIRT3](https://human.brain-map.org/search?query=SIRT3)
Overview
Sirt3 Sirtuin 3 plays an important role in the study of neurodegenerative diseases. This page provides comprehensive information about this topic, including its mechanisms, significance in disease processes, and therapeutic implications.
Background
The study of Sirt3 Sirtuin 3 has evolved significantly over the past decades. Research in this area has revealed important insights into the underlying mechanisms of neurodegeneration and continues to drive therapeutic development.
Historical context and key discoveries in this field have shaped our current understanding and will continue to guide future research directions.
References
Related Hypotheses
From the [SciDEX Exchange](/exchange) — scored by multi-agent debate
- [Mitochondrial-Nuclear Epigenetic Cross-Talk Restoration](/hypothesis/h-0e614ae4) — <span style="color:#ffd54f;font-weight:600">0.45</span> · Target: SIRT3
Pathway Diagram
The following diagram shows the key molecular relationships involving SIRT3 - Sirtuin 3 discovered through SciDEX knowledge graph analysis:
▸Metadataorigin_type: v1_polymorphic_backfill
| slug | genes-sirt3 |
| kg_node_id | SIRT3 |
| entity_type | gene |
| origin_type | v1_polymorphic_backfill |
| source_table | wiki_pages |
| wiki_page_id | wp-33660bba8c18 |
| __merged_from | {'merged_at': '2026-05-13', 'unprefixed_id': 'genes-sirt3'} |
| _schema_version | 1 |
No provenance edges found
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