MAP1S: Microtubule-Associated Protein 1S

A key regulator of autophagy, mitophagy, and genome stability, implicated in cancer and neurodegenerative disorders.

Gene Information Card

Symbol MAP1S
Full Name Microtubule-Associated Protein 1S
Gene Type Protein coding
Chromosomal Location 19p13.11
NCBI Gene ID 55201 ncbi.nlm.nih.gov/gene/55201
Ensembl ID ENSG00000167286
UniProt ID Q66K74
OMIM ID 609267
HGNC ID 15719
Aliases MAP1A/1B light chain 3 related protein, MAP1S_HUMAN, C19orf5, MAP1A/1BLC3, MTAP1S

Description

MAP1S (Microtubule-Associated Protein 1S) encodes a protein that belongs to the microtubule-associated protein 1 family. It functions as a scaffold linking microtubules to autophagic machinery, facilitating autophagy and mitophagy. MAP1S also plays a role in maintaining genome stability by promoting DNA repair and regulating the mitotic spindle. Its dysregulation is linked to various cancers and neurodegenerative diseases.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Hepatocellular carcinoma MAP1S loss impairs autophagy, leading to accumulation of damaged organelles and genomic instability, promoting tumorigenesis. PMID: 21804562
Prostate cancer Reduced MAP1S expression correlates with poor prognosis; loss of MAP1S enhances cell proliferation and invasion via defective mitophagy. PMID: 23376921
Alzheimer's disease MAP1S deficiency impairs clearance of tau aggregates and damaged mitochondria, contributing to neuronal cell death. PMID: 24908484
Parkinson's disease MAP1S-mediated mitophagy is critical for removing dysfunctional mitochondria; loss of MAP1S exacerbates dopaminergic neuron loss. PMID: 26912668

Expression Profile

Tissue Expression
Tissue nTPM level
Liver 12.5 Medium
Brain 8.3 Low
Heart 6.1 Low
Kidney 9.7 Low
Testis 15.2 Medium
Cell Line Expression
Cell Line nTPM Notes
HepG2 (liver cancer) 14.8 High expression
SH-SY5Y (neuroblastoma) 7.2 Moderate expression
HeLa (cervical cancer) 10.1 Moderate expression
MCF7 (breast cancer) 5.6 Low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.487C>T (p.Arg163*) Nonsense <0.1% Loss of function; truncation of protein, likely impairing autophagy
c.632A>G (p.Glu211Gly) Missense <0.1% Unknown; predicted to affect protein stability
c.1015_1016insA (p.Thr339Asnfs*12) Frameshift <0.1% Loss of function; premature stop codon
Mutation functional classification

Loss of Function (LOF)

Nonsense and frameshift mutations (e.g., p.Arg163*, p.Thr339Asnfs*12) lead to truncated or unstable protein, impairing autophagy and mitophagy.

Gain of Function (GOF)

No gain-of-function mutations reported in MAP1S.

Dominant Negative (DN)

No dominant-negative mutations reported in MAP1S.

Pathways

Autophagy - Homo sapiens (human) (KEGG: hsa04140)
Mitophagy - animal (Reactome: R-HSA-5205647)
Cellular responses to stress (Reactome: R-HSA-2262752)

Protein Summary

The MAP1S protein (UniProt Q66K74) is a 1,099-amino-acid microtubule-associated protein that contains an N-terminal microtubule-binding domain and a C-terminal region that interacts with LC3/GABARAP family proteins. It acts as a molecular linker between microtubules and the autophagic machinery, promoting autophagosome formation and maturation. MAP1S also localizes to the mitotic spindle and centrosomes, where it contributes to chromosome segregation and genomic stability. Post-translational modifications include phosphorylation and ubiquitination, which regulate its stability and function.

Related Products

Product name Cat.No. Species Gene ID
MAP1S Knockout HEK293 Cell Line EDJ-KQ14193 Human 55201 Details Get a Quote
MAP1S Knockout A-549 Cell Line EDJ-KQ44135 Human 55201 Details Get a Quote
MAP1S Knockout HCT 116 Cell Line EDJ-KQ44136 Human 55201 Details Get a Quote
MAP1S Knockout HeLa Cell Line EDJ-KQ44137 Human 55201 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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