FEBS Letters | |
Cloning of the mouse phospholipid hydroperoxide glutathione peroxidase gene | |
Schnurr, Kerstin1  Kühn, Hartmut1  Borchert, Astrid1  Thiele, Bernd J1  | |
[1] Institute of Biochemistry, University Clinics (Charité), Humboldt University, Hessiche Str. 3–4, 10115 Berlin, Germany | |
关键词: Atherogenesis; Inflammation; Lipid peroxidation; Oxidative stress; Selenium; SECIS; selenocysteine insertion sequence; PH-GPx; phospholipid hydroperoxide glutathione peroxidase; GPx; glutathione peroxidase; | |
DOI : 10.1016/S0014-5793(99)00221-5 | |
学科分类:生物化学/生物物理 | |
来源: John Wiley & Sons Ltd. | |
【 摘 要 】
15-Lipoxygenases and phospholipid hydroperoxide glutathione peroxidases (PH-GPx) are counterparts in the metabolism of hydroperoxy lipids and a balanced regulation of both enzymes appears to be important for the cellular peroxide tone regulating the expression of redox sensitive genes. In contrast to lipoxygenases the molecular biology of PH-GPx is less well investigated. In this study we cloned the PH-GPx cDNA from a mouse fibroblast cDNA library and the PH-GPx gene from a mouse genomic library. The gene spans approximately 4 kb which includes 1 kb of 5′-flanking region and consists of seven exons and six introns. The immediate promoter region does not contain a TATA box but there are binding sites for several transcription factors which also occur in the porcine gene. Our investigations provide useful tools for future targeted gene disruption studies.
【 授权许可】
Unknown
【 预 览 】
Files | Size | Format | View |
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RO201912020307394ZK.pdf | 199KB | download |