OASL: 2'-5'-Oligoadenylate Synthetase Like

Interferon-induced antiviral and tumor suppressor gene

Gene Information Card

Symbol OASL
Full Name 2'-5'-Oligoadenylate Synthetase Like
Gene Type Protein coding
Chromosomal Location 12q24.31
NCBI Gene ID 8638 ncbi.nlm.nih.gov/gene/8638
Ensembl ID ENSG00000135114
UniProt ID Q15646
OMIM ID 603281
HGNC ID 8090
Aliases TRIP14, OASL1, p59 OASL, OASLd

Description

OASL (2'-5'-Oligoadenylate Synthetase Like) is an interferon-inducible gene that encodes a protein belonging to the 2'-5'-oligoadenylate synthetase family. Unlike classical OAS enzymes, OASL lacks canonical 2'-5'-oligoadenylate synthetase activity but plays a critical role in antiviral innate immunity by enhancing RIG-I signaling and modulating interferon responses. It is also implicated in tumor suppression and autoimmune regulation.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Viral infections (e.g., influenza, hepatitis C) OASL enhances RIG-I-mediated interferon induction, restricting viral replication PMID: 21957124
Systemic lupus erythematosus (SLE) OASL overexpression linked to interferon signature and autoimmunity PMID: 25605271
Colorectal cancer OASL acts as a tumor suppressor via modulation of interferon signaling and apoptosis PMID: 31570879
Breast cancer OASL expression correlates with prognosis and immune infiltration PMID: 32697978

Expression Profile

Tissue Expression
Tissue nTPM level
Lung 12.5 Medium
Spleen 18.3 Medium
Liver 8.9 Low
Small intestine 15.1 Medium
Whole blood 5.2 Low
Cell Line Expression
Cell Line nTPM Notes
HeLa 22.4 High expression
A549 16.8 Medium expression
HepG2 10.3 Low expression
MCF7 14.7 Medium expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1045C>T (p.Arg349Trp) Missense 0.001% (gnomAD) Unknown functional impact
c.1282G>A (p.Glu428Lys) Missense 0.002% (gnomAD) Potential loss of interferon induction
c.1546_1547insA Frameshift <0.001% Predicted loss of function
Mutation functional classification

Loss of Function (LOF)

Frameshift and nonsense variants that truncate the protein likely impair OASL's ability to enhance RIG-I signaling.

Gain of Function (GOF)

No confirmed gain-of-function mutations reported.

Dominant Negative (DN)

Not established; potential dominant-negative effects of missense variants remain uncharacterized.

Pathways

RIG-I/MDA5 mediated induction of interferon-alpha/beta (Reactome: R-HSA-168928)
Interferon alpha/beta signaling (Reactome: R-HSA-909733)
Antiviral mechanism by IFN-stimulated genes (Reactome: R-HSA-1169410)

Protein Summary

The OASL protein (59 kDa) contains a single N-terminal nucleotidyltransferase domain and two C-terminal ubiquitin-like domains. It lacks the canonical DFD motif required for 2'-5'-oligoadenylate synthesis but retains RNA binding ability. OASL amplifies RIG-I signaling by mimicking polyubiquitin chains, promoting IRF3 and NF-κB activation. It is strongly induced by type I interferons and plays a dual role in antiviral defense and cancer modulation.

Related Products

Product name Cat.No. Species Gene ID
OASL Knockout HEK293 Cell Line EDJ-KQ6317 Human 8638 Details Get a Quote
OASL Knockout HeLa Cell Line EDJ-KQ28929 Human 8638 Details Get a Quote
OASL Knockout A-549 Cell Line EDJ-KQ30239 Human 8638 Details Get a Quote
OASL Knockout HCT 116 Cell Line EDJ-KQ30240 Human 8638 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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