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Glutathione peroxidase 4 - Wikipedia Jump to content

Glutathione peroxidase 4

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GPX4
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesGPX4, GPx-4, GSHPx-4, MCSP, PHGPx, snGPx, snPHGPx, SMDS, glutathione peroxidase 4
External IDsOMIM: 138322; MGI: 104767; HomoloGene: 134384; GeneCards: GPX4; OMA:GPX4 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

2879

625249

Ensembl

ENSG00000167468

ENSMUSG00000075706

UniProt

P36969

Q76LV0
O70325

RefSeq (mRNA)

NM_002085
NM_001039847
NM_001039848
NM_001367832

NM_001037741
NM_008162
NM_001367995

RefSeq (protein)

NP_001034936
NP_001034937
NP_002076
NP_001354761

NP_001032830.2
NP_001032830
NP_032188
NP_001354924

Location (UCSC)Chr 19: 1.1 – 1.11 MbChr 10: 79.88 – 79.89 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Glutathione peroxidase 4, also known as GPX4, is an enzyme that in humans is encoded by the GPX4 gene.[5] GPX4 is a phospholipid hydroperoxidase that protects cells against membrane lipid peroxidation.

Discovery

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GPX4 was first discovered in biochemistry laboratories of the University of Padua, where it was described as an enzyme capable of protecting against peroxidation. Its role as an inhibitor of cellular death was only discovered in 2012 by a research group Columbia University.

Function

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The antioxidant enzyme glutathione peroxidase 4 (GPX4) belongs to the family of glutathione peroxidases, which consists of 8 known mammalian isoenzymes (GPX1–8). GPX4 catalyzes the reduction of hydrogen peroxide, organic hydroperoxides, and lipid peroxides at the expense of reduced glutathione and functions in the protection of cells against oxidative stress. The oxidized form of glutathione (glutathione disulfide), which is generated during the reduction of hydroperoxides by GPX4, is recycled by glutathione reductase and NADPH/H+. GPX4 differs from the other GPX family members in terms of its monomeric structure, a less restricted dependence on glutathione as reducing substrate, and the ability to reduce lipid-hydroperoxides inside biological membranes.

Inactivation of GPX4 leads to an accumulation of lipid peroxides, resulting in ferroptotic cell death.[6][7] Mutations in GPX4 cause spondylometaphyseal dysplasia.[8] In vitro studies suggest that GPX4 protects cells against cold-induced cell death.[9][unreliable source]

Structure

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Mammalian GPX1, GPX2, GPX3, and GPX4 (this protein) have been shown to be selenium-containing enzymes, whereas GPX6 is a selenoprotein in humans with cysteine-containing homologues in rodents. In selenoproteins, the amino acid selenocysteine is inserted in the nascent polypeptide chain during the process of translational recoding of the UGA stop codon. GPX4 shares the amino acid motif of selenocysteine, glutamine, and tryptophan (catalytic triad) with other glutathione peroxidases.

Reaction mechanism

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GPX4 catalyzes the following reaction:

This reaction occurs at the selenocysteine within the catalytic center of GPX4. During the catalytic cycle of GPX4, the active selenol (-SeH) is oxidized by peroxides to selenenic acid (-SeOH), which is then reduced with glutathione (GSH) to an intermediate selenodisulfide (-Se-SG). GPX4 is eventually reactivated by a second glutathione molecule, releasing glutathione disulfide (GS-SG).

Subcellular distribution of isoforms

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In mouse and rat, three distinct GPX4 isoforms with different subcellular localization are produced through alternative splicing and transcription initiation; cytosolic GPX4, mitochondrial GPX4 (mGPX4), and nuclear GPX4 (nGPX4). Cytosolic GPX4 has been identified as the only GPX4 isoform being essential for embryonic development and cell survival. The GPX4 isoforms mGPX4 and nGPX4 have been implicated in spermatogenesis and male fertility.[10] In humans, experimental evidence for alternative splicing exists; alternative transcription initiation and the cleavage sites of the mitochondrial and nuclear transit peptides need to be experimentally verified.[11]

Animal models

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Knockout mice of GPX4 die at embryonic day 8[12][13] and conditional inducible deletion in adult mice (neurons) results in degeneration and death in less than a month.[14] Targeted disruption of the mitochondrial GPX4 isoform (mGPX4) caused infertility in male mice and disruption of the nuclear GPX4 isoform (nGPX4) reduced the structural stability of sperm chromatin, yet both knockout mouse models (for mGPX4 and nGPX4) were fully viable. Surprisingly, knockout of GPX4 heterozygously in mice (GPX4+/−) increases their median life span.[15] Knockout studies with GPX1, GPX2, or GPX3 deficient mice showed that cytosolic GPX4 is so far the only glutathione peroxidase that is indispensable for embryonic development and cell survival. As mechanisms to dispose of both hydrogen peroxide and lipid hydroperoxides are essential to life, this indicates that in contrast to the multiple metabolic pathways that can be utilized to dispose of hydrogen peroxide, pathways for the disposal of lipid hydroperoxides are limited.

While mammals have only one copy of the GPX4 gene, fish have two copies, GPX4a and GPX4b.[16] The GPX4's appear to play a greater role in the fish GPX system than in mammals. For example, in fish GPX4 activity contributes to a greater extent to total GPX activity,[17] GPX4a is the most highly expressed selenoprotein mRNA (in contrast to mammals where it is GPX1 mRNA)[18] and GPX4a appears to be highly inducible to changes within the cellular environment, such as changes in methylmercury and selenium status.[19]

Pathology

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The interaction of GPX4 with the autophagic degradation pathway further modulates cell's response to oxidative stress. Impaired GPX4 function plays a role in tumorigenesis, neurodegeneration, infertility, inflammation, immune disorders, and ischemia-reperfusion injury. Additionally, the R152H mutation in GPX4 is involved in the development of Sedaghatian-type spinal metaphyseal dysplasia, a rare and fatal disease in newborn babies.[20]

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000167468 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000075706 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Esworthy RS, Doan K, Doroshow JH, Chu FF (July 1994). "Cloning and sequencing of the cDNA encoding a human testis phospholipid hydroperoxide glutathione peroxidase". Gene. 144 (2): 317–8. doi:10.1016/0378-1119(94)90400-6. PMID 8039723.
  6. ^ Yang WS, Sriramaratnam R, Welsch ME, Shimada K, Skouta R, Viswanathan VS, Cheah JH, Clemons PA, Shamji AF, Clish CB, Brown LM, Girotti AW, Cornish VW, Schreiber SL, Stockwell BR (16 January 2014). "Regulation of ferroptotic cancer cell death by GPX4". Cell. 156 (1–2): 317–31. doi:10.1016/j.cell.2013.12.010. PMC 4076414. PMID 24439385.
  7. ^ Friedmann Angeli JP, Schneider M, Proneth B, Tyurina YY, Tyurin VA, Hammond VJ, Herbach N, Aichler M, Walch A, Eggenhofer E, Basavarajappa D, Rådmark O, Kobayashi S, Seibt T, Beck H, Neff F, Esposito I, Wanke R, Förster H, Yefremova O, Heinrichmeyer M, Bornkamm GW, Geissler EK, Thomas SB, Stockwell BR, o'Donnell VB, Kagan VE, Schick JA, Conrad M (17 November 2014). "Inactivation of the ferroptosis regulator Gpx4 triggers acute renal failure in mice". Nature Cell Biology. 16 (12): 1180–1191. doi:10.1038/ncb3064. PMC 4894846. PMID 25402683.
  8. ^ Smith AC, Mears AJ, Bunker R, Ahmed A, MacKenzie M, Schwartzentruber JA, Beaulieu CL, Ferretti E, Majewski J, Bulman DE, Celik FC, Boycott KM, Graham GE, Graham GE (2014). "Mutations in the enzyme glutathione peroxidase 4 cause Sedaghatian-type spondylometaphyseal dysplasia". Journal of Medical Genetics. 51 (7): 470–4. doi:10.1136/jmedgenet-2013-102218. PMID 24706940. S2CID 22887914.
  9. ^ Lam B, Kajderowicz KM, Keys HR, Roessler JM, Frenkel EM, Kirkland A, Bisht P, El-Brolosy MA, Jaenisch R, Bell GW, Weissman JS, Griffith EC, Hrvatin S (July 2024). "Multi-species genome-wide CRISPR screens identify GPX4 as a conserved suppressor of cold-induced cell death". BioRxiv: The Preprint Server for Biology. doi:10.1101/2024.07.25.605098. PMC 11291167. PMID 39091747.
  10. ^ Schneider M, Förster H, Boersma A, Seiler A, Wehnes H, Sinowatz F, Neumüller C, Deutsch MJ, Walch A, Hrabé de Angelis M, Wurst W, Ursini F, Roveri A, Maleszewski M, Maiorino M, Conrad M (May 2009). "Mitochondrial glutathione peroxidase 4 disruption causes male infertility" (PDF). FASEB J. 23 (9): 3233–42. doi:10.1096/fj.09-132795. PMID 19417079. S2CID 11610232.
  11. ^ "Entrez Gene: GPX4 glutathione peroxidase 4 (phospholipid hydroperoxidase)".
  12. ^ Yant LJ, Ran Q, Rao L, Van Remmen H, Shibatani T, Belter JG, Motta L, Richardson A, Prolla TA (February 2003). "The selenoprotein GPX4 is essential for mouse development and protects from radiation and oxidative damage insults". Free Radic. Biol. Med. 34 (4): 496–502. doi:10.1016/S0891-5849(02)01360-6. PMID 12566075.
  13. ^ Muller FL, Lustgarten MS, Jang Y, Richardson A, Van Remmen H (2007). "Trends in oxidative aging theories". Free Radic. Biol. Med. 43 (4): 477–503. doi:10.1016/j.freeradbiomed.2007.03.034. PMID 17640558.
  14. ^ Seiler A, Schneider M, Förster H, Roth S, Wirth EK, Culmsee C, Plesnila N, Kremmer E, Rådmark O, Wurst W, Bornkamm GW, Schweizer U, Conrad M (September 2008). "Glutathione peroxidase 4 senses and translates oxidative stress into 12/15-lipoxygenase dependent- and AIF-mediated cell death". Cell Metab. 8 (3): 237–48. doi:10.1016/j.cmet.2008.07.005. PMID 18762024.
  15. ^ Ran Q, Liang H, Ikeno Y, Qi W, Prolla TA, Roberts LJ, Wolf N, Van Remmen H, VanRemmen H, Richardson A (2007). "Reduction in glutathione peroxidase 4 increases life span through increased sensitivity to apoptosis". J. Gerontol. A Biol. Sci. Med. Sci. 62 (9): 932–42. doi:10.1093/gerona/62.9.932. PMID 17895430.
  16. ^ Mariotti M, Ridge PG, Zhang Y, Lobanov AV, Pringle TH, Guigo R, Hatfield DL, Gladyshev VN (2012). "Composition and evolution of the vertebrate and mammalian selenoproteomes". PLOS ONE. 7 (3): e33066. Bibcode:2012PLoSO...733066M. doi:10.1371/journal.pone.0033066. PMC 3316567. PMID 22479358.
  17. ^ Grim JM, Hyndman KA, Kriska T, Girotti AW, Crockett EL (2011). "Relationship between oxidizable fatty acid content and level of antioxidant glutathione peroxidases in marine fish". The Journal of Experimental Biology. 214 (22): 3751–3759. doi:10.1242/jeb.058214. PMC 3202513. PMID 22031739.
  18. ^ Zheng W, Xu H, Lam SH, Luo H, Karuturi RK, Gong Z (2013). "Transcriptomic analyses of sexual dimorphism of the zebrafish liver and the effect of sex hormones". PLOS ONE. 8 (1): e53562. Bibcode:2013PLoSO...853562Z. doi:10.1371/journal.pone.0053562. PMC 3547925. PMID 23349717.
  19. ^ Penglase S, Hamre K, Ellingsen S (2014). "Selenium prevents downregulation of antioxidant selenoprotein genes by methylmercury". Free Radical Biology and Medicine. 75: 95–104. doi:10.1016/j.freeradbiomed.2014.07.019. hdl:1956/8708. PMID 25064324.
  20. ^ Xie Y, Kang R, Klionsky DJ, Tang D (2023). "GPX4 in cell death, autophagy, and disease". Autophagy. 19 (10): 2621–2638. doi:10.1080/15548627.2023.2218764. PMC 10472888. PMID 37272058.

Further reading

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  • Overview of all the structural information available in the PDB for UniProt: P36969 (Phospholipid hydroperoxide glutathione peroxidase) at the PDBe-KB.
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