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Microtubule-associated protein 1 light chain 3 gamma (MAP1LC3C)

Target
MAP1LC3C
Molecular classification
Ubiquitin-like modifier, Autophagy-related protein, Microtubule-associated protein, ATG8 protein family member
01

Overview

Microtubule-associated protein 1 light chain 3 gamma (MAP1LC3C) is a ubiquitin-like autophagy-related protein and member of the ATG8 family[5][6]. It is involved in the selective and bulk autophagy processes, especially through recruitment and interaction with adapter proteins presenting LC3-interacting regions (LIRs)[2][4]. MAP1LC3C distinguishes itself by a unique N-terminal extension containing a polyproline II motif and a phosphorylation-regulated interface, contributing to specific microtubule and protein interactions; its principal roles encompass autophagosome formation, elongation, selective cargo recognition, and degradation of intracellular pathogens and protein aggregates[4][6]. Pathological relevance includes neurodegenerative diseases, hereditary spastic paraplegia, antibacterial responses, and selective autophagy in cancer and cellular differentiation[5][6][1]. Robust antibody specificity and aggregation tendencies present challenges for both research and potential therapeutic exploitation[6].

Other names
Microtubule-associated protein 1 light chain 3 gammaMAP1LC3CMicrotubule-associated proteins 1A/1B light chain 3CMAP1A/MAP1B LC3 CATG8JAutophagy-related protein LC3 CAutophagy-related ubiquitin-like modifier LC3 CMAP1 light chain 3-like protein 3LC3CMAP1A/MAP1B light chain 3 Cmicrotubule-associated proteins 1A/1B light chain 3C
02

Mechanism of action

Drugs modulating autophagy (e.g., autophagy inducers or inhibitors) may influence MAP1LC3C-dependent pathways, typically by affecting autophagosome formation or lysosomal fusion, but MAP1LC3C is not a direct drug target according to current data[5][6].

03

Biological functions

Autophagy (formation and elongation of autophagosomes)Selective autophagy (xenophagy, aggrephagy)Microtubule bindingCargo recognition (via LC3-interacting region/LIR domains)Regulation of cellular differentiation (e.g., odontogenic differentiation)
04

Disease associations

Neurodegenerative disease (Frontotemporal dementia, Amyotrophic lateral sclerosis)Hereditary spastic paraplegiaCancer (roles in senescence, autophagy)Infection (antibacterial autophagy/xenophagy)Other (potential in degenerative and differentiation disorders)
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Safety considerations

Overexpression leads to protein aggregation, complicating therapeutic strategies and antibody developmentFunctional redundancy and weak expression in normal tissues may limit specificity or biomarker utility
06

Biomarkers

MAP1LC3C expression or localization could serve as a biomarker for selective autophagy, autophagosome formation, or possibly disease differentiation where expression patterns are altered (e.g., neurodegenerative disease, cancer)

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