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TERC Gene
TERC Gene
Introduction
<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">TERC Gene</th>
</tr>
<tr>
<td class="label">Symbol</td>
<td>TERC</td>
</tr>
<tr>
<td class="label">Full Name</td>
<td>Telomerase RNA Component</td>
</tr>
<tr>
<td class="label">Chromosomal Location</td>
<td>3q26.2</td>
</tr>
<tr>
<td class="label">NCBI Gene ID</td>
<td>7012</td>
</tr>
<tr>
<td class="label">OMIM</td>
<td>602322</td>
</tr>
<tr>
<td class="label">Ensembl ID</td>
<td>ENSG00000264364</td>
</tr>
<tr>
<td class="label">RNA Type</td>
<td>Long non-coding RNA (lncRNA)</td>
</tr>
<tr>
<td class="label">Length</td>
<td>~451 nucleotides</td>
</tr>
<tr>
<td class="label">Associated Diseases</td>
<td><a href="/wiki/als" style="color:#ef9a9a">ALS</a>, <a href="/wiki/aging" style="color:#ef9a9a">Aging</a>, <a href="/wiki/als" style="color:#ef9a9a">Als</a>, <a href="/wiki/cancer" style="color:#ef9a9a">Cancer</a>, <a href="/wiki/inflammation" style="color:#ef9a9a">Inflammation</a></td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">39 edges</a></td>
</tr>
</table>
Terc Gene is an important component in the neurobiology of neurodegenerative diseases. This page provides detailed information about its structure, function, and role in disease processes.
Overview
...TERC Gene
Introduction
<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">TERC Gene</th>
</tr>
<tr>
<td class="label">Symbol</td>
<td>TERC</td>
</tr>
<tr>
<td class="label">Full Name</td>
<td>Telomerase RNA Component</td>
</tr>
<tr>
<td class="label">Chromosomal Location</td>
<td>3q26.2</td>
</tr>
<tr>
<td class="label">NCBI Gene ID</td>
<td>7012</td>
</tr>
<tr>
<td class="label">OMIM</td>
<td>602322</td>
</tr>
<tr>
<td class="label">Ensembl ID</td>
<td>ENSG00000264364</td>
</tr>
<tr>
<td class="label">RNA Type</td>
<td>Long non-coding RNA (lncRNA)</td>
</tr>
<tr>
<td class="label">Length</td>
<td>~451 nucleotides</td>
</tr>
<tr>
<td class="label">Associated Diseases</td>
<td><a href="/wiki/als" style="color:#ef9a9a">ALS</a>, <a href="/wiki/aging" style="color:#ef9a9a">Aging</a>, <a href="/wiki/als" style="color:#ef9a9a">Als</a>, <a href="/wiki/cancer" style="color:#ef9a9a">Cancer</a>, <a href="/wiki/inflammation" style="color:#ef9a9a">Inflammation</a></td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">39 edges</a></td>
</tr>
</table>
Terc Gene is an important component in the neurobiology of neurodegenerative diseases. This page provides detailed information about its structure, function, and role in disease processes.
Overview
TERC (Telomerase RNA Component, also known as hTR) encodes the RNA component of human telomerase, which is essential for maintaining telomere length at chromosome ends. Telomeres are repetitive DNA sequences (TTAGGG repeats in vertebrates) that protect chromosome ends from degradation and fusion events. TERC serves as the template for telomeric DNA synthesis, while the catalytic subunit TERT (TERT Gene) provides the reverse transcriptase activity. Together, they form the active telomerase complex that adds telomeric repeats to counteract the telomere shortening that occurs with each cell division. [@greider1993]
Gene Information
Molecular Function
Telomere Elongation Template
TERC functions as the RNA template for telomere synthesis. The conserved sequence region within TERC contains the template region (CUAACCCUAAC) that directs the addition of TTAGGG repeats to the 3' end of telomeres [1]. This template function is essential for:
- Maintaining chromosomal stability
- Preventing replicative senescence
- Enabling continued cell division in stem cells and cancer cells
Telomerase Complex Assembly
TERC interacts with multiple proteins to form the telomerase holoenzyme:
- TERT (Telomerase Reverse Transcriptase): The catalytic subunit that uses TERC as template
- DKC1 (Dyskerin): Essential for RNA stability and telomerase assembly
- GAR1, NHP2, NOP10: Additional assembly factors
- TCAB1 (WRAP53): Guides telomerase to Cajal bodies for maturation
Structural Features
TERC contains several functional domains:
Expression and Regulation
TERC is highly expressed in:
- Embryonic stem cells and germ cells
- Activated lymphocytes
- Hematopoietic stem cells
- Certain neuronal populations
Expression is downregulated in most somatic cells with age, contributing to cellular senescence.
Role in Neurodegeneration
Telomere Syndromes and Neurological Manifestations
Mutations in TERC cause several telomere biology disorders with significant neurological components:
- X-linked form caused by DKC1 mutations affects TERC stability
- Neurological symptoms: developmental delay, intellectual disability, cerebellar ataxia
- Progressive bone marrow failure leading to premature death
- TERC mutations cause bone marrow failure
- Secondary neurological complications from hypoxia
- TERC mutations associated with lung fibrosis
- May have CNS involvement through unknown mechanisms
Telomere Length in Neurodegenerative Diseases
While TERC mutations cause rare telomere syndromes, telomere shortening has been implicated in several neurodegenerative conditions:
- Alzheimer's Disease: Shorter telomere length in peripheral blood cells associated with increased AD risk [2]
- Parkinson's Disease: Telomere shortening observed in PD patients; LRRK2 mutations may affect telomere maintenance
- Amyotrophic Lateral Sclerosis (ALS): TERT expression reduced in ALS motor [neurons](/entities/neurons)
- Huntington's Disease: Telomere attrition correlates with disease progression
Mechanisms Linking Telomere Biology to Neurodegeneration
Therapeutic Implications
Telomerase Activators
- TA-65: A cycloastragenol-derived compound that activates telomerase
- Shows promise in improving immune function and reducing senescence markers
Gene Therapy Approaches
- TERC gene delivery using AAV vectors in preclinical models
- mRNA-based TERC delivery for transient activation
Challenges
- Telomerase activation could promote cancer growth
- Careful dosing and targeting required
- [Blood-brain barrier](/entities/blood-brain-barrier) limits CNS delivery
Interactions and Pathway
The TERC-containing telomerase complex interacts with multiple cellular pathways involved in neurodegeneration:
- DNA damage response pathways (ATM, ATR, p53)
- Mitochondrial function and oxidative stress response
- Stem cell maintenance and self-renewal
- Cellular senescence pathways
Key Publications
See Also
- [TERT Gene](/genes/tert)
- [DKC1 Gene](/genes/dkc1)
- [Telomere Biology](/mechanisms/telomere-maintenance)
- [Dyskeratosis Congenita](/diseases/dyskeratosis-congenita)
- [Alzheimer's Disease Mechanisms](/mechanisms/alzheimers-disease-pathogenesis)
- [Parkinson's Disease Mechanisms](/diseases/parkinsons-disease-mechanisms)
External Links
- [NCBI Gene: TERC](https://www.ncbi.nlm.nih.gov/gene/7012)
- [OMIM: TERC](https://www.omim.org/entry/602322)
- [Ensembl: TERC](https://www.ensembl.org/Homo_sapiens/Gene/Summary?g=ENSG00000264364)
- [UniProt: TERC](https://www.uniprot.org/uniprot/Q9URQ2)
Background
The study of Terc Gene 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
- [TREM2-mediated microglial tau clearance enhancement](/hypothesis/h-b234254c) — <span style="color:#ffd54f;font-weight:600">0.55</span> · Target: TREM2
- [HSP90-Tau Disaggregation Complex Enhancement](/hypothesis/h-0f00fd75) — <span style="color:#ffd54f;font-weight:600">0.55</span> · Target: HSP90AA1
- [VCP-Mediated Autophagy Enhancement](/hypothesis/h-18a0fcc6) — <span style="color:#ffd54f;font-weight:600">0.54</span> · Target: VCP
- [LRP1-Dependent Tau Uptake Disruption](/hypothesis/h-4dd0d19b) — <span style="color:#ffd54f;font-weight:600">0.53</span> · Target: LRP1
- [Synaptic Vesicle Tau Capture Inhibition](/hypothesis/h-73e29e3a) — <span style="color:#ffd54f;font-weight:600">0.40</span> · Target: SNAP25
- [Trans-Synaptic Adhesion Molecule Modulation](/hypothesis/h-fdaae8d9) — <span style="color:#ff8a65;font-weight:600">0.40</span> · Target: NLGN1
- [Extracellular Vesicle Biogenesis Modulation](/hypothesis/h-55ef81c5) — <span style="color:#ff8a65;font-weight:600">0.40</span> · Target: CHMP4B
Related Analyses:
- [Tau propagation mechanisms and therapeutic interception points](/analysis/SDA-2026-04-02-gap-tau-prop-20260402003221) 🔄
- [Tau propagation mechanisms and therapeutic interception points](/analysis/SDA-2026-04-02-gap-tau-propagation-20260402) 🔄
Pathway Diagram
The following diagram shows the key molecular relationships involving TERC Gene discovered through SciDEX knowledge graph analysis:
▸Metadataorigin_type: v1_polymorphic_backfill
| slug | genes-terc |
| kg_node_id | TERC |
| entity_type | gene |
| origin_type | v1_polymorphic_backfill |
| source_table | wiki_pages |
| wiki_page_id | wp-c98a4f2e816b |
| __merged_from | {'merged_at': '2026-05-13', 'unprefixed_id': 'genes-terc'} |
| _schema_version | 1 |
No provenance edges found
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[TERC Gene](http://scidex.ai/artifact/wiki-genes-terc)
http://scidex.ai/artifact/wiki-genes-terc