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MAP1LC3B — LC3B
MAP1LC3B — Microtubule-Associated Protein 1 Light Chain 3 Beta (LC3B)
<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">MAP1LC3B — LC3B</th>
</tr>
<tr>
<td class="label"><strong>Gene Symbol</strong></td>
<td>MAP1LC3B</td>
</tr>
<tr>
<td class="label"><strong>Full Name</strong></td>
<td>Microtubule-associated proteins 1A/1B light chain 3B</td>
</tr>
<tr>
<td class="label"><strong>Chromosomal Location</strong></td>
<td>16q24.2</td>
</tr>
<tr>
<td class="label"><strong>NCBI Gene ID</strong></td>
<td>81631</td>
</tr>
<tr>
<td class="label"><strong>OMIM</strong></td>
<td>609605</td>
</tr>
<tr>
<td class="label"><strong>Ensembl ID</strong></td>
<td>ENSG00000140941</td>
</tr>
<tr>
<td class="label"><strong>UniProt ID</strong></td>
<td>Q9GZQ8</td>
</tr>
<tr>
<td class="label"><strong>Protein Length</strong></td>
<td>125 amino acids</td>
</tr>
<tr>
<td class="label"><strong>Molecular Weight</strong></td>
<td>~14.5 kDa</td>
</tr>
<tr>
<td class="label"><strong>Expression</strong></td>
<td>Ubiquitous, high in brain (neurons and glia), liver, heart, skeletal muscle</td>
</tr>
<tr>
<td class="label">Receptor</td>
<td>Target</td>
</tr>
<tr>
<td class="label">p62/SQSTM1</td>
<td>Protein aggregates</td>
</tr>
<tr>
<td class="label">OPTN</td>
<td>Mitochondria (mitophagy)</td>
</tr>
<tr>
<td class="label">NDP52</td>
<td>Mitochondria (mitophagy)</td>
</tr>
<tr>
<td class="label">Ta
MAP1LC3B — Microtubule-Associated Protein 1 Light Chain 3 Beta (LC3B)
<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">MAP1LC3B — LC3B</th>
</tr>
<tr>
<td class="label"><strong>Gene Symbol</strong></td>
<td>MAP1LC3B</td>
</tr>
<tr>
<td class="label"><strong>Full Name</strong></td>
<td>Microtubule-associated proteins 1A/1B light chain 3B</td>
</tr>
<tr>
<td class="label"><strong>Chromosomal Location</strong></td>
<td>16q24.2</td>
</tr>
<tr>
<td class="label"><strong>NCBI Gene ID</strong></td>
<td>81631</td>
</tr>
<tr>
<td class="label"><strong>OMIM</strong></td>
<td>609605</td>
</tr>
<tr>
<td class="label"><strong>Ensembl ID</strong></td>
<td>ENSG00000140941</td>
</tr>
<tr>
<td class="label"><strong>UniProt ID</strong></td>
<td>Q9GZQ8</td>
</tr>
<tr>
<td class="label"><strong>Protein Length</strong></td>
<td>125 amino acids</td>
</tr>
<tr>
<td class="label"><strong>Molecular Weight</strong></td>
<td>~14.5 kDa</td>
</tr>
<tr>
<td class="label"><strong>Expression</strong></td>
<td>Ubiquitous, high in brain (neurons and glia), liver, heart, skeletal muscle</td>
</tr>
<tr>
<td class="label">Receptor</td>
<td>Target</td>
</tr>
<tr>
<td class="label">p62/SQSTM1</td>
<td>Protein aggregates</td>
</tr>
<tr>
<td class="label">OPTN</td>
<td>Mitochondria (mitophagy)</td>
</tr>
<tr>
<td class="label">NDP52</td>
<td>Mitochondria (mitophagy)</td>
</tr>
<tr>
<td class="label">Tax1BP1</td>
<td>Damaged organelles</td>
</tr>
<tr>
<td class="label">Mechanism</td>
<td>Evidence</td>
</tr>
<tr>
<td class="label">Impaired autophagic flux</td>
<td>LC3-positive vesicles accumulate in AD brains</td>
</tr>
<tr>
<td class="label">Amyloid-beta clearance</td>
<td>Autophagy degrades Aβ; dysfunction reduces clearance</td>
</tr>
<tr>
<td class="label">Tau pathology</td>
<td>Autophagy modulates tau aggregation and clearance</td>
</tr>
<tr>
<td class="label">Synaptic dysfunction</td>
<td>LC3B localizes to synapses; altered in AD</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/alzheimer" style="color:#ef9a9a">Alzheimer</a>, <a href="/wiki/alzheimer's-disease" style="color:#ef9a9a">Alzheimer's disease</a></td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">1288 edges</a></td>
</tr>
</table>
Pathway Diagram
Introduction
MAP1LC3B encodes microtubule-associated protein 1 light chain 3 beta (LC3B), a key protein in the autophagy pathway. LC3B is essential for autophagosome formation and serves as a reliable marker for autophagy activity. It belongs to the LC3/GABARAP family of proteins, which are the mammalian homologs of yeast Atg8 [@kabeya2000][@nixon2007].
LC3B plays critical roles in protein quality control, organelle clearance, and cellular homeostasis—processes that are fundamentally impaired in neurodegenerative diseases. The protein's involvement in selective autophagy pathways, including mitophagy (mitochondrial clearance) and aggrephagy (protein aggregate clearance), makes it a central player in neurodegeneration [@chut2009][@rubinsztein2010].
Gene Information
Normal Function
MAP1LC3B encodes LC3B, a key protein in the autophagy pathway. LC3B is essential for autophagosome formation and serves as a reliable marker for autophagy activity. The protein undergoes post-translational modifications crucial for its function [@komatsu2012][@kimmelman2015].
Structure and Isoforms
The LC3 family includes several isoforms:
Each isoform has distinct functions in different autophagy pathways.
The Autophagy Process
LC3B participates in all stages of autophagy:
1. Initiation
- ULK1 complex activates autophagy
- LC3B precursor is processed
2. Nucleation
- Beclin1-VPS34 complex forms
- PI3P production recruits LC3B
3. Expansion
- LC3-I is conjugated to phosphatidylethanolamine (PE)
- LC3-II (lipidated form) is generated
- LC3-II localizes to the autophagosome membrane
- Links cargo to autophagic machinery
4. Fusion
- Autophagosome fuses with lysosome
- LC3-II is degraded inside
LC3 Lipidation
The key post-translational modification is lipidation:
- LC3-I: Cytosolic form, unconjugated
- LC3-II: Phosphatidylethanolamine-conjugated form, membrane-bound
During autophagy, LC3-I is conjugated to phosphatidylethanolamine (PE) by the ATG7 (E1-like) and ATG3 (E2-like) enzymes, generating LC3-II. LC3-II localizes to the autophagosome membrane and is involved in:
- Autophagosome nucleation and expansion
- Selective cargo recognition (via autophagy receptors like p62/SQSTM1)
- Fusion with lysosomes
- Protein aggregate clearance
Selective Autophagy
LC3B is crucial for selective autophagy receptors:
Autophagy in Neurons
Neurons have unique autophagy requirements:
- Post-mitotic: Cannot divide to dilute damaged components
- High energy demand: Requires efficient mitochondria
- Long lifespan: Must maintain function for decades
- Complex morphology: Requires autophagy throughout axons/dendrites
Autophagy is essential for:
- Synaptic plasticity
- Mitochondrial quality control
- Protein aggregate clearance
- Axonal transport
- Neuronal survival
Disease Associations
Alzheimer's Disease
LC3B dysfunction significantly contributes to AD pathogenesis:
Key findings:
- Accumulation of LC3-positive autophagic vacuoles in AD brains
- Reduced lysosomal function impairs LC3 turnover
- p62 and LC3 colocalize with amyloid plaques
- Autophagy-lysosomal pathway dysfunction is an early event
Parkinson's Disease
LC3B is central to PD through mitophagy:
- PINK1 phosphorylates LC3B to initiate mitophagy
- Loss of LC3B function impairs mitochondrial clearance
- Alpha-synuclein toxicity affects autophagy
- Genetic variants modify PD risk
Huntington's Disease
- Reduced autophagy leads to mutant huntingtin accumulation
- LC3B function impaired by mutant huntingtin
- Autophagy induction is therapeutic in HD models
Lysosomal Storage Disorders
- Impaired autophagosome-lysosome fusion
- LC3B accumulation due to blocked degradation
- Contributes to neurodegeneration
Expression Regulation
MAP1LC3B is ubiquitously expressed with high levels in:
- Brain (neurons and glia)
- Liver
- Heart
- Skeletal muscle
Expression is regulated by:
- Nutrient status (downregulated during starvation—actually increases during starvation)
- mTOR signaling (inhibition promotes LC3 expression)
- TFEB (transcription factor for autophagy genes)
- Oxidative stress
- ER stress
- Hypoxia
Therapeutic Implications
Therapeutic approaches targeting MAP1LC3B/autophagy include:
Autophagy Induction
- mTOR inhibitors (rapamycin): Promote autophagy
- Carbamazepine: Beclin-1 independent autophagy
- Metformin: AMPK-dependent autophagy
- Lithium: Inositol depletion, autophagy enhancement
Autophagy Enhancement
- TFEB activators: Increase autophagy gene expression
- Small molecule autophagy enhancers: Improve clearance
- Beclin-1 modulators: Enhance nucleation
Targeting Specific Pathways
- Mitophagy inducers: Enhance PINK1/Parkin pathway
- Aggrephagy enhancers: Promote aggregate clearance
- Lysosomal function enhancers: Improve degradation
Cross-Links
- [Alzheimer's Disease](/diseases/alzheimers-disease) — Primary disease association
- [Parkinson's Disease](/diseases/parkinsons-disease) — Mitophagy dysfunction
- [Autophagy-Lysosomal Pathway](/mechanisms/autophagy-lysosomal-pathway) — Core pathway
- [LC3B Protein](/proteins/lc3b-protein) — Related protein page
- [p62/SQSTM1](/proteins/p62-protein) — Autophagy receptor
- [ATG7](/genes/atg7) — LC3-conjugating enzyme
- [Mitophagy Pathway](/mechanisms/mitophagy) — Selective autophagy
- [Protein Aggregation Pathway](/mechanisms/protein-aggregation) — Aggregate clearance
Key Publications
See Also
- [Autophagy Pathway](/mechanisms/autophagy)
- [Mitophagy Pathway](/mechanisms/mitophagy)
- [Lysosomal Pathway](/mechanisms/lysosomal-pathway)
- [Protein Quality Control](/mechanisms/protein-quality-control-network)
- [Alzheimer's Disease](/diseases/alzheimers-disease)
- [Parkinson's Disease](/diseases/parkinsons-disease)
References
Pathway Diagram
The following diagram shows the key molecular relationships involving MAP1LC3B — LC3B discovered through SciDEX knowledge graph analysis:
▸Metadataorigin_type: v1_polymorphic_backfill
| slug | genes-map1lc3b |
| kg_node_id | MAP1LC3B |
| entity_type | gene |
| origin_type | v1_polymorphic_backfill |
| source_table | wiki_pages |
| wiki_page_id | wp-23bf08dd0c0e |
| __merged_from | {'merged_at': '2026-05-13', 'unprefixed_id': 'genes-map1lc3b'} |
| _schema_version | 1 |
No provenance edges found
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[MAP1LC3B — LC3B](http://scidex.ai/artifact/wiki-genes-map1lc3b)
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