| ID | Sequence | Length | GC content |
|---|---|---|---|
| AUUGGUCGGCUGGACGAGGGGAGGAGCCGCUGGCUCCCAGCCCCGCCGC… | 873 nt | 0.6208 | |
| AGUCCUGACUACGGCCUCCGGGCCCUUUGUCCCCGCUAGCGGCGCUCGG… | 997 nt | 0.6499 | |
| GCCUUUGCCGCCUACUGAAGCCGGCGCUGCUCUGUGGGGCUCUGGCCGC… | 788 nt | 0.6129 | |
| AUUGGUCGGCUGGACGAGGGGAGGAGCCGCUGGCUCCCAGCCCCGCCGC… | 851 nt | 0.6228 |
The protein encoded by this gene belongs to the glutathione peroxidase family, members of which catalyze the reduction of hydrogen peroxide, organic hydroperoxides and lipid hydroperoxides, and thereby protect cells against oxidative damage. Several isozymes of this gene family exist in vertebrates, which vary in cellular location and substrate specificity. This isozyme has a high preference for lipid hydroperoxides and protects cells against membrane lipid peroxidation and cell death. It is also required for normal sperm development; thus, it has been identified as a 'moonlighting' protein because of its ability to serve dual functions as a peroxidase, as well as a structural protein in mature spermatozoa. Mutations in this gene are associated with Sedaghatian type of spondylometaphyseal dysplasia (SMDS). This isozyme is also a selenoprotein, containing the rare amino acid selenocysteine (Sec) at its active site. Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. Transcript variants resulting from alternative splicing or use of alternate promoters have been described to encode isoforms with different subcellular localization. [provided by RefSeq, Dec 2018]
A study in rats demonstrated that skeletal muscle contusion induces ferroptosis, evidenced by significantly decreased GPX4 protein levels alongside increased Fe2+ and MDA, with these effects being reversed by ferroptosis inhibitors [Yang et al. DOI:10.3390/ijms252011317]. In human HT-29 cells exposed to arsenic trioxide, immunoblotting showed no significant change in GPX4 protein levels, indicating its expression was not altered under those specific heavy metal exposure conditions [Kazuta et al. DOI:10.1016/J.Legalmed.2026.102774].