Target intelligence / Profile preview

Long intergenic non-coding RNA for adipogenesis and lipogenesis (linc-ADAL)

Target
linc-ADAL
Molecular classification
Long non-coding RNA (lncRNA), RNA regulatory molecule (not a protein, enzyme, or receptor)
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Overview

Long intergenic non-coding RNA for adipogenesis and lipogenesis (linc-ADAL) is a non-coding RNA molecule, located between the AQPEP and AP3S1 genes on human chromosome 5. It is highly enriched in adipose tissue and plays a pivotal role in regulating the differentiation of preadipocytes into mature adipocytes and in promoting lipid accumulation. Mechanistically, linc-ADAL directly interacts with hnRNPU (a nuclear protein) and IGF2BP2 (a cytoplasmic mRNA-binding protein) at different subcellular sites to coordinate gene expression programs necessary for adipogenesis and lipogenesis. Knockdown studies show that loss of linc-ADAL impairs both adipocyte maturation and expression of key genes involved in lipid synthesis. It is under study as a key factor associated with obesity and metabolic diseases, but is not itself currently a drug target

Other names
linc-ADALlincRNA for adipogenesis and lipogenesisLINC-ADALLINCADL
02

Mechanism of action

Not applicable; linc-ADAL is not targeted by drugs, but acts by regulating gene expression through interaction with nuclear (hnRNPU) and cytoplasmic (IGF2BP2) proteins involved in adipocyte differentiation and lipid metabolism

03

Biological functions

Adipocyte differentiation (adipogenesis)Lipogenesis regulation (fatty acid synthesis in adipose tissue)Interacts with proteins such as hnRNPU and IGF2BP2 to control gene expression in fat cells
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Disease associations

ObesityMetabolic disorders (through its impact on fat tissue development and lipid storage)
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Safety considerations

None reported. No safety or toxicity issues are attributed to linc-ADAL itself, as it is an endogenous regulatory RNA and not a therapeutic target or drug.
06

Biomarkers

Expression of linc-ADAL is a marker for mature adipocytes and is highly enriched in human adipose tissue. Its expression correlates with adipose tissue status and may be explored as a biomarker in studies of obesity and fat metabolism.

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