| ID | Sequence | Length | GC content |
|---|---|---|---|
| AGGAGAGAAGACGUGCAGGGACCCCGCGCACAGGAGCUGCCCUCGCGAC… | 1257 nt | 0.5465 | |
| AGGAGAGAAGACGUGCAGGGACCCCGCGCACAGGAGCUGCCCUCGCGAC… | 1233 nt | 0.5556 | |
| AGGAGAGAAGACGUGCAGGGACCCCGCGCACAGGAGCUGCCCUCGCGAC… | 1221 nt | 0.5594 | |
| AGGAGAGAAGACGUGCAGGGACCCCGCGCACAGGAGCUGCCCUCGCGAC… | 1368 nt | 0.5592 |
This gene encodes the receptor for urokinase plasminogen activator and, given its role in localizing and promoting plasmin formation, likely influences many normal and pathological processes related to cell-surface plasminogen activation and localized degradation of the extracellular matrix. It binds both the proprotein and mature forms of urokinase plasminogen activator and permits the activation of the receptor-bound pro-enzyme by plasmin. The protein lacks transmembrane or cytoplasmic domains and may be anchored to the plasma membrane by a glycosyl-phosphatidylinositol (GPI) moiety following cleavage of the nascent polypeptide near its carboxy-terminus. However, a soluble protein is also produced in some cell types. Alternative splicing results in multiple transcript variants encoding different isoforms. The proprotein experiences several post-translational cleavage reactions that have not yet been fully defined. [provided by RefSeq, Jul 2008]
A study in rats demonstrated that the PLAUR gene, identified via RNA sequencing, was significantly upregulated at 1, 4, and 7 days after spinal cord injury [Li et al. DOI:10.4103/1673-5374.255994]. In a separate study in weanling swine, microarray analysis showed the PLAUR transcript was significantly increased in skin at 7 days postexposure to both sulfur mustard and thermal burn injury, identifying it as a potential therapeutic target for wound healing [Price et al. DOI:10.080/15569520903097754].