Molecular biology of glutathione peroxidase 4: from genomic structure to developmental expression and neural function
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Nicolai E. Savaskan
Abstract
Selenoproteins have been recognized as modulators of brain function and signaling. Phospholipid hydroperoxide glutathione peroxidase (GPx4/PHGPx) is a unique member of the selenium-dependent glutathione peroxidases in mammals with a pivotal role in brain development and function. GPx4 exists as a cytosolic, mitochondrial, and nuclear isoform derived from a single gene. In mice, the GPx4 gene is located on chromosome 10 in close proximity to a functional retrotransposome that is expressed under the control of captured regulatory elements. Elucidation of crystallographic data uncovered structural peculiarities of GPx4 that provide the molecular basis for its unique enzymatic properties and substrate specificity. Monomeric GPx4 is multifunctional: it acts as a reducing enzyme of peroxidized phospholipids and thiols and as a structural protein. Transcriptional regulation of the different GPx4 isoforms requires several isoform-specific cis-regulatory sequences and trans-activating factors. Cytosolic and mitochondrial GPx4 are the major isoforms exclusively expressed by neurons in the developing brain. In stark contrast, following brain trauma, GPx4 is specifically upregulated in non-neuronal cells, i.e., reactive astrocytes. Molecular approaches to genetic modification in mice have revealed an essential and isoform-specific function for GPx4 in development and disease. Here we review recent findings on GPx4 with emphasis on its molecular structure and function and consider potential mechanisms that underlie neural development and neuropathological conditions.
©2007 by Walter de Gruyter Berlin New York
Artikel in diesem Heft
- Selenoproteins – biochemistry and clinical relevance
- Selenium in mammalian spermiogenesis
- Selenium in chemistry and biochemistry in comparison to sulfur
- Molecular biology of glutathione peroxidase 4: from genomic structure to developmental expression and neural function
- Physiological role of phospholipid hydroperoxide glutathione peroxidase in mammals
- Activation of the glutathione peroxidase 2 (GPx2) promoter by β-catenin
- Effect of age on sexually dimorphic selenoprotein expression in mice
- Post-translational processing of selenoprotein P: implications of glycosylation for its utilisation by target cells
- Selenoproteins of the thyroid gland: expression, localization and possible function of glutathione peroxidase 3
- Towards understanding selenocysteine incorporation into bacterial proteins
- Glutathione- and thioredoxin-related enzymes are modulated by sulfur-containing chemopreventive agents
- B- and T-cell-specific inactivation of thioredoxin reductase 2 does not impair lymphocyte development and maintenance
- Effect of selenium on thioredoxin reductase activity in Txnrd1 or Txnrd2 hemizygous mice
- Influence of pH and flanking serine on the redox potential of S-S and S-Se bridges of Cys-Cys and Cys-Sec peptides
- An essential role for Pin1 in Xenopus laevis embryonic development revealed by specific inhibitors
- Glucocorticoid receptor-mediated expression of kallikrein 10 in human breast cancer cell lines
Artikel in diesem Heft
- Selenoproteins – biochemistry and clinical relevance
- Selenium in mammalian spermiogenesis
- Selenium in chemistry and biochemistry in comparison to sulfur
- Molecular biology of glutathione peroxidase 4: from genomic structure to developmental expression and neural function
- Physiological role of phospholipid hydroperoxide glutathione peroxidase in mammals
- Activation of the glutathione peroxidase 2 (GPx2) promoter by β-catenin
- Effect of age on sexually dimorphic selenoprotein expression in mice
- Post-translational processing of selenoprotein P: implications of glycosylation for its utilisation by target cells
- Selenoproteins of the thyroid gland: expression, localization and possible function of glutathione peroxidase 3
- Towards understanding selenocysteine incorporation into bacterial proteins
- Glutathione- and thioredoxin-related enzymes are modulated by sulfur-containing chemopreventive agents
- B- and T-cell-specific inactivation of thioredoxin reductase 2 does not impair lymphocyte development and maintenance
- Effect of selenium on thioredoxin reductase activity in Txnrd1 or Txnrd2 hemizygous mice
- Influence of pH and flanking serine on the redox potential of S-S and S-Se bridges of Cys-Cys and Cys-Sec peptides
- An essential role for Pin1 in Xenopus laevis embryonic development revealed by specific inhibitors
- Glucocorticoid receptor-mediated expression of kallikrein 10 in human breast cancer cell lines
