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NOSTRIN Gene
NOSTRIN Gene
<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">NOSTRIN Gene</th>
</tr>
<tr>
<td class="label">Symbol</td>
<td>NOSTRIN</td>
</tr>
<tr>
<td class="label">Full Name</td>
<td>Nitric Oxide Synthase Trafficking Inducer</td>
</tr>
<tr>
<td class="label">Chromosome</td>
<td>2q31.1</td>
</tr>
<tr>
<td class="label">NCBI Gene ID</td>
<td>[54112](https://www.ncbi.nlm.nih.gov/gene/54112)</td>
</tr>
<tr>
<td class="label">OMIM ID</td>
<td>[609046](https://www.omim.org/entry/609046)</td>
</tr>
<tr>
<td class="label">UniProt ID</td>
<td>[Q9NRC8](https://www.uniprot.org/uniprot/Q9NRC8)</td>
</tr>
<tr>
<td class="label">Ensembl ID</td>
<td>ENSG00000163050</td>
</tr>
<tr>
<td class="label">Protein Family</td>
<td>F-Box only protein</td>
</tr>
<tr>
<td class="label">Molecular Weight</td>
<td>~60 kDa</td>
</tr>
<tr>
<td class="label">Expression</td>
<td>Brain, endothelium, heart</td>
</tr>
<tr>
<td class="label">Tissue Specificity</td>
<td>Ubiquitous with highest in brain</td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">1 edges</a></td>
</tr>
</table>
NOSTRIN Gene
<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">NOSTRIN Gene</th>
</tr>
<tr>
<td class="label">Symbol</td>
<td>NOSTRIN</td>
</tr>
<tr>
<td class="label">Full Name</td>
<td>Nitric Oxide Synthase Trafficking Inducer</td>
</tr>
<tr>
<td class="label">Chromosome</td>
<td>2q31.1</td>
</tr>
<tr>
<td class="label">NCBI Gene ID</td>
<td>[54112](https://www.ncbi.nlm.nih.gov/gene/54112)</td>
</tr>
<tr>
<td class="label">OMIM ID</td>
<td>[609046](https://www.omim.org/entry/609046)</td>
</tr>
<tr>
<td class="label">UniProt ID</td>
<td>[Q9NRC8](https://www.uniprot.org/uniprot/Q9NRC8)</td>
</tr>
<tr>
<td class="label">Ensembl ID</td>
<td>ENSG00000163050</td>
</tr>
<tr>
<td class="label">Protein Family</td>
<td>F-Box only protein</td>
</tr>
<tr>
<td class="label">Molecular Weight</td>
<td>~60 kDa</td>
</tr>
<tr>
<td class="label">Expression</td>
<td>Brain, endothelium, heart</td>
</tr>
<tr>
<td class="label">Tissue Specificity</td>
<td>Ubiquitous with highest in brain</td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">1 edges</a></td>
</tr>
</table>
NOSTRIN (Nitric Oxide Synthase Trafficking Inducer) is a scaffolding protein that plays a critical role in regulating nitric oxide (NO) signaling in the nervous and vascular systems. By modulating the subcellular localization and activity of neuronal nitric oxide synthase (nNOS), NOSTRIN influences nitric oxide production, which is essential for normal neuronal function but can contribute to excitotoxicity and neurodegeneration when dysregulated.
Gene Overview
Background
NOSTRIN was originally identified as a binding partner of neuronal nitric oxide synthase (nNOS, encoded by [NOS1](/genes/nos1)). The protein contains multiple protein-protein interaction domains, including an F-box domain that allows it to recruit nNOS to specific subcellular compartments.
The name NOSTRIN reflects its primary function—acting as a "trafficking inducer" that directs nNOS to particular cellular locations, thereby controlling where nitric oxide is produced and what signaling pathways are activated.
Protein Structure
NOSTRIN contains several functional domains:
Normal Function
Nitric Oxide Signaling Regulation
NOSTRIN performs several critical functions in nitric oxide signaling:
Neurophysiological Roles
Synaptic Transmission
- NO acts as a retrograde neurotransmitter/modulator
- NOSTRIN regulates this signaling at synapses
- Controls timing and specificity of NO-mediated signaling
Blood Flow Regulation
- In endothelial cells, NOSTRIN influences NOS trafficking
- Regulates cerebral blood flow
- Maintains [blood-brain barrier](/entities/blood-brain-barrier) function
Neuroprotection
- Appropriate NO signaling has neuroprotective effects
- NOSTRIN helps maintain this balance
- Prevents excessive NO production
Molecular Interactions
NOSTRIN interacts with several key proteins:
- nNOS (NOS1): Primary binding partner; NOSTRIN recruits nNOS to membranes and dendritic compartments
- PSD-95: Targets nNOS to postsynaptic densities
- CAPON: Competes with NOSTRIN for nNOS binding
- 14-3-3 Proteins: Regulate NOSTRIN stability and localization
- NOSIP: Co-regulator of nNOS localization
Expression Pattern
Brain Expression
- [Hippocampus](/brain-regions/hippocampus): CA1-CA3 regions, dentate gyrus - high expression
- Cerebral [Cortex](/brain-regions/cortex): All layers, particularly layer V pyramidal neurons
- Cerebellum: Purkinje cells and granule cells
- Substantia Nigra: Dopaminergic neurons
- Brainstem: Various nuclei including locus coeruleus
- Hypothalamus: Moderate expression
- Amygdala: High expression in central nucleus
Cellular Localization
- Neurons: Cytosolic with membrane association
- Dendrites: Concentrated in dendritic shafts and spines
- Synapses: Presynaptic and postsynaptic localization
- Endothelium: Membrane-bound in vascular endothelial cells
Peripheral Expression
- Endothelium: High expression in vascular endothelial cells throughout body
- Heart: Cardiac myocytes, particularly in ventricles
- Liver: Hepatocytes
- Kidney: Tubular epithelial cells
- Skeletal Muscle: Muscle fibers
Disease Associations
Alzheimer's Disease (AD)
NOSTRIN dysfunction contributes to Alzheimer's pathogenesis through multiple mechanisms:
Excitotoxicity
- Dysregulated nNOS localization leads to excessive NO production
- Contributes to excitotoxic neuronal death
- Synaptic [NMDA receptor](/entities/nmda-receptor) activation triggers NOSTRIN-dependent pathways
Amyloid-beta Effects
- [Aβ](/proteins/amyloid-beta) oligomers can alter NOSTRIN expression and function
- NOSTRIN dysfunction exacerbates Aβ-induced toxicity
- Alters nNOS coupling to amyloid pathology
Vascular Dysfunction
- Impaired NO signaling affects cerebral blood flow
- Blood-brain barrier integrity compromised
- Contributes to vascular contributions to cognitive impairment
Synaptic Failure
- Abnormal NO signaling disrupts synaptic plasticity mechanisms
- [LTP](/mechanisms/long-term-potentiation) deficits in NOSTRIN-dysregulated systems
- Memory consolidation affected
Parkinson's Disease (PD)
In Parkinson's disease:
Dopaminergic Neuron Vulnerability
- NOSTRIN dysfunction may contribute to specific vulnerability of dopaminergic neurons
- NO signaling in substantia nigra particularly sensitive
- nNOS upregulation in PD brains
Neuroinflammation
- NO signaling modulates microglial activation
- NOSTRIN alterations affect inflammatory responses
- Chronic neuroinflammation
Mitochondrial Dysfunction
- Interactions between NO signaling and mitochondrial health
- NOSTRIN affects nNOS-mitochondria coupling
- Energy metabolism disruption
Stroke and Vascular Dementia
- Cerebral Ischemia: NOSTRIN expression altered after stroke
- Recovery: Affects post-ischemic plasticity
- Vascular Cognitive Impairment: Regulates cerebral blood flow through endothelial NO signaling
Other Neurodegenerative Conditions
- Multiple Sclerosis: NOSTRIN affects demyelination and neuroinflammation
- Amyotrophic Lateral Sclerosis (ALS): Altered NO signaling contributes to motor neuron degeneration
- Depression and Anxiety: NOSTRIN dysfunction may affect mood through NO signaling
- Huntington's Disease: Altered NO signaling in striatum
Therapeutic Implications
Drug Targets
- nNOS Inhibitors: Selective nNOS inhibitors may be beneficial in conditions with NOSTRIN dysfunction
- NOSTRIN Modulators: Compounds that restore proper nNOS trafficking
- NO Scavengers: In conditions with excessive NO production
Biomarkers
- NOSTRIN expression levels in blood or CSF may indicate NOS dysregulation
- NOSTRIN fragments as disease progression markers
Gene Therapy Approaches
- Restoring proper NOSTRIN function to normalize NO signaling
- AAV-delivered NOSTRIN variants
- CRISPR-based corrections
Small Molecule Development
- NOSTRIN-nNOS interaction disruptors
- F-box mimetics
- Membrane-targeted NO modulators
Animal Models
Knockout Studies
NOSTRIN-deficient mice exhibit:
- Altered nNOS subcellular localization in hippocampus
- Behavioral changes related to NO signaling
- Vascular function abnormalities
- Impaired spatial memory
Transgenic Models
- NOSTRIN overexpression affects synaptic plasticity
- Interactions with Alzheimer's disease models
- Protective effects in some paradigms
Disease Models
- NOSTRIN in MPTP Parkinson's model
- NOSTRIN in stroke models
- NOSTRIN in amyloid models
Signaling Pathways
NOSTRIN-nNOS Signaling
Downstream Effectors
- Soluble Guanylate Cyclase (sGC): Primary NO receptor
- cGMP-dependent Protein Kinase (PKG): Mediates many NO effects
- cGMP-gated Channels: Ion flux regulation
- ADP-ribosylation: Direct protein modification
See Also
- [Genes Index](/genes)
- [NOS1 Gene](/proteins/nos1)
- [Nitric Oxide Signaling](/mechanisms/nitric-oxide-signaling-neurodegeneration)
- [Endothelial Function](/genes/nct)
- [Alzheimer's Disease](/diseases/alzheimers-disease)
- [Parkinson's Disease](/diseases/parkinsons-disease)
- [Excitotoxicity](/mechanisms/excitotoxicity-neurodegeneration)
- [Synaptic Plasticity](/mechanisms/synaptic-plasticity)
- [Blood-Brain Barrier](/entities/blood-brain-barrier)
- [Neuroinflammation](/mechanisms/neuroinflammation-pathway)
External Links
- [NCBI Gene - NOSTRIN](https://www.ncbi.nlm.nih.gov/gene/54112)
- [UniProt - NOSTRIN](https://www.uniprot.org/uniprot/Q9NRC8)
- [Ensembl - NOSTRIN](https://www.ensembl.org/Homo_sapiens/Gene/Summary?g=ENSG00000163050)
- [GeneCards - NOSTRIN](https://www.genecards.org/cgi-bin/carddisp.pl?gene=NOSTRIN)
- [HGNC - NOSTRIN](https://www.genenames.org/data/hgnc_data.php?hgnc_id=17878)
References
▸Metadataorigin_type: v1_polymorphic_backfill
| slug | genes-nostrin |
| kg_node_id | NOSTRIN |
| entity_type | gene |
| origin_type | v1_polymorphic_backfill |
| source_table | wiki_pages |
| wiki_page_id | wp-065f77bd0149 |
| __merged_from | {'merged_at': '2026-05-13', 'unprefixed_id': 'genes-nostrin'} |
| _schema_version | 1 |
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