Cloning of the mouse phospholipid hydroperoxide glutathione peroxidase gene
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 t...
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Veröffentlicht in: | FEBS letters 1999-03, Vol.446 (2), p.223-227 |
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creator | Borchert, Astrid Schnurr, Kerstin Thiele, Bernd J Kühn, Hartmut |
description | 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. |
doi_str_mv | 10.1016/S0014-5793(99)00221-5 |
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Our investigations provide useful tools for future targeted gene disruption studies.</description><subject>Animals</subject><subject>Atherogenesis</subject><subject>Base Sequence</subject><subject>Cloning, Molecular</subject><subject>DNA, Complementary</subject><subject>Glutathione Peroxidase - genetics</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Lipid peroxidation</subject><subject>Mice</subject><subject>Molecular Sequence Data</subject><subject>Oxidative stress</subject><subject>Selenium</subject><subject>Sequence Homology, Nucleic Acid</subject><subject>Swine</subject><issn>0014-5793</issn><issn>1873-3468</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kE1LxDAQhoMo7rr6E5SeRA_VpGnT5CTL4hcueFDPIW2m20jb1KQV99-b_dDDMMzwzMs7L0LnBN8QTNjtG8YkjbNc0CshrjFOEhJnB2hKeE5jmjJ-iKb_yASdeP-Jw8yJOEaToIAxT7Mpelk0tjPdKrJVNNQQtXb0EPW19aEa0xsd1WvtbA_O_hgN0aoZBzXUxnYB2y1VuFhBB6foqFKNh7N9n6GPh_v3xVO8fH18XsyXMSSMDrFKOFeacVxSQjTVuqjSilSaclLlRLOcC0EzLnKuCKuA4TRPSqwLkRBeUJ3RGbrc6fbOfo3gB9kaX0LTqA6CfckEywRON-DFHhyLFrTsnWmVW8u_9wNwtwMg2P024KQvDXQlaOOgHKS2JsAbnslt4HKTphRCbgOXGf0F8c9x-w</recordid><startdate>19990312</startdate><enddate>19990312</enddate><creator>Borchert, Astrid</creator><creator>Schnurr, Kerstin</creator><creator>Thiele, Bernd J</creator><creator>Kühn, Hartmut</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>19990312</creationdate><title>Cloning of the mouse phospholipid hydroperoxide glutathione peroxidase gene</title><author>Borchert, Astrid ; Schnurr, Kerstin ; Thiele, Bernd J ; Kühn, Hartmut</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-e263t-a288ad680c311d3ddbf4f1fd381f71d67899358978a16fe60472c0db9218b3d53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Animals</topic><topic>Atherogenesis</topic><topic>Base Sequence</topic><topic>Cloning, Molecular</topic><topic>DNA, Complementary</topic><topic>Glutathione Peroxidase - genetics</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Lipid peroxidation</topic><topic>Mice</topic><topic>Molecular Sequence Data</topic><topic>Oxidative stress</topic><topic>Selenium</topic><topic>Sequence Homology, Nucleic Acid</topic><topic>Swine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Borchert, Astrid</creatorcontrib><creatorcontrib>Schnurr, Kerstin</creatorcontrib><creatorcontrib>Thiele, Bernd J</creatorcontrib><creatorcontrib>Kühn, Hartmut</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>FEBS letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Borchert, Astrid</au><au>Schnurr, Kerstin</au><au>Thiele, Bernd J</au><au>Kühn, Hartmut</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cloning of the mouse phospholipid hydroperoxide glutathione peroxidase gene</atitle><jtitle>FEBS letters</jtitle><addtitle>FEBS Lett</addtitle><date>1999-03-12</date><risdate>1999</risdate><volume>446</volume><issue>2</issue><spage>223</spage><epage>227</epage><pages>223-227</pages><issn>0014-5793</issn><eissn>1873-3468</eissn><abstract>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. 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subjects | Animals Atherogenesis Base Sequence Cloning, Molecular DNA, Complementary Glutathione Peroxidase - genetics Humans Inflammation Lipid peroxidation Mice Molecular Sequence Data Oxidative stress Selenium Sequence Homology, Nucleic Acid Swine |
title | Cloning of the mouse phospholipid hydroperoxide glutathione peroxidase gene |
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