Genomic Organization and Regulation by Dietary Fat of the Uncoupling Protein 3 and 2 Genes
Uncoupling protein-1 (UCP1) dissipates the transmitochondrial proton gradient as heat. UCP2 and UCP3 are two recently discovered homologues that also have uncoupling activity and thus presumably have a role in energy homeostasis. We now report the genomic structure of murine UCP3 (7 exons) and UCP2...
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Veröffentlicht in: | Biochemical and biophysical research communications 1999-03, Vol.256 (1), p.27-32 |
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description | Uncoupling protein-1 (UCP1) dissipates the transmitochondrial proton gradient as heat. UCP2 and UCP3 are two recently discovered homologues that also have uncoupling activity and thus presumably have a role in energy homeostasis. We now report the genomic structure of murine UCP3 (7 exons) and UCP2 (8 exons). UCP3 is ∼8 kilobases upstream of UCP2. An UCP3 variant mRNA, UCP3S, was also found and characterized. The effect of a high fat diet (45% versus 10%) on UCP3 and UCP2 mRNA levels was measured. Eating the 45% fat diet for eight weeks caused greater weight gain in AKR and C57BL/6J mice than in the obesity-resistant A/J mice. The high fat diet increased muscle UCP3 expression twofold in C57BL/6J animals. UCP2 expression increased slightly on the 45% fat diet in white adipose of AKR mice, but not in A/J or C57BL/6J mice. In skeletal muscle, UCP2 expression showed little variation with diet. Thus, UCP2 and UCP3 expression levels change in response to diet-induced obesity, but the changes are modest and depend on the tissue and genotype. The data suggest that it is not a reduction in UCP2 or UCP3 expression that causes obesity in the susceptible mice. |
doi_str_mv | 10.1006/bbrc.1999.0239 |
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UCP2 and UCP3 are two recently discovered homologues that also have uncoupling activity and thus presumably have a role in energy homeostasis. We now report the genomic structure of murine UCP3 (7 exons) and UCP2 (8 exons). UCP3 is ∼8 kilobases upstream of UCP2. An UCP3 variant mRNA, UCP3S, was also found and characterized. The effect of a high fat diet (45% versus 10%) on UCP3 and UCP2 mRNA levels was measured. Eating the 45% fat diet for eight weeks caused greater weight gain in AKR and C57BL/6J mice than in the obesity-resistant A/J mice. The high fat diet increased muscle UCP3 expression twofold in C57BL/6J animals. UCP2 expression increased slightly on the 45% fat diet in white adipose of AKR mice, but not in A/J or C57BL/6J mice. In skeletal muscle, UCP2 expression showed little variation with diet. Thus, UCP2 and UCP3 expression levels change in response to diet-induced obesity, but the changes are modest and depend on the tissue and genotype. The data suggest that it is not a reduction in UCP2 or UCP3 expression that causes obesity in the susceptible mice.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1006/bbrc.1999.0239</identifier><identifier>PMID: 10066417</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adipose Tissue - metabolism ; Alternative Splicing ; Amino Acid Sequence ; Animals ; Carrier Proteins - genetics ; Cloning, Molecular ; diet induced obesity ; Dietary Fats - administration & dosage ; Dietary Fats - pharmacology ; Disease Susceptibility ; Exons - genetics ; Gene Expression Regulation ; Humans ; Ion Channels ; Membrane Transport Proteins ; Mice ; Mice, Inbred Strains ; Mitochondrial Proteins ; Molecular Sequence Data ; Muscle, Skeletal - metabolism ; Obesity - chemically induced ; Obesity - genetics ; Polymerase Chain Reaction ; Protein Isoforms - genetics ; Proteins - genetics ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Sequence Homology, Amino Acid ; thermogenesis ; Uncoupling Protein 2 ; Uncoupling Protein 3 ; uncoupling proteins</subject><ispartof>Biochemical and biophysical research communications, 1999-03, Vol.256 (1), p.27-32</ispartof><rights>1999 Academic Press</rights><rights>Copyright 1999 Academic Press.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c371t-be3f25f8e55b104bf0a658dbd4745ec2ac5a4a8a363eb05718d3393be4d005863</citedby><cites>FETCH-LOGICAL-c371t-be3f25f8e55b104bf0a658dbd4745ec2ac5a4a8a363eb05718d3393be4d005863</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1006/bbrc.1999.0239$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10066417$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gong, Da-Wei</creatorcontrib><creatorcontrib>He, Yufang</creatorcontrib><creatorcontrib>Reitman, Marc L.</creatorcontrib><title>Genomic Organization and Regulation by Dietary Fat of the Uncoupling Protein 3 and 2 Genes</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>Uncoupling protein-1 (UCP1) dissipates the transmitochondrial proton gradient as heat. UCP2 and UCP3 are two recently discovered homologues that also have uncoupling activity and thus presumably have a role in energy homeostasis. We now report the genomic structure of murine UCP3 (7 exons) and UCP2 (8 exons). UCP3 is ∼8 kilobases upstream of UCP2. An UCP3 variant mRNA, UCP3S, was also found and characterized. The effect of a high fat diet (45% versus 10%) on UCP3 and UCP2 mRNA levels was measured. Eating the 45% fat diet for eight weeks caused greater weight gain in AKR and C57BL/6J mice than in the obesity-resistant A/J mice. The high fat diet increased muscle UCP3 expression twofold in C57BL/6J animals. UCP2 expression increased slightly on the 45% fat diet in white adipose of AKR mice, but not in A/J or C57BL/6J mice. In skeletal muscle, UCP2 expression showed little variation with diet. Thus, UCP2 and UCP3 expression levels change in response to diet-induced obesity, but the changes are modest and depend on the tissue and genotype. The data suggest that it is not a reduction in UCP2 or UCP3 expression that causes obesity in the susceptible mice.</description><subject>Adipose Tissue - metabolism</subject><subject>Alternative Splicing</subject><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Carrier Proteins - genetics</subject><subject>Cloning, Molecular</subject><subject>diet induced obesity</subject><subject>Dietary Fats - administration & dosage</subject><subject>Dietary Fats - pharmacology</subject><subject>Disease Susceptibility</subject><subject>Exons - genetics</subject><subject>Gene Expression Regulation</subject><subject>Humans</subject><subject>Ion Channels</subject><subject>Membrane Transport Proteins</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Mitochondrial Proteins</subject><subject>Molecular Sequence Data</subject><subject>Muscle, Skeletal - metabolism</subject><subject>Obesity - chemically induced</subject><subject>Obesity - genetics</subject><subject>Polymerase Chain Reaction</subject><subject>Protein Isoforms - genetics</subject><subject>Proteins - genetics</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Sequence Homology, Amino Acid</subject><subject>thermogenesis</subject><subject>Uncoupling Protein 2</subject><subject>Uncoupling Protein 3</subject><subject>uncoupling proteins</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM9LwzAUx4Mobk6vHiUnb61J059HmW4Kg4k4EC8hSV9npE1m0grzr7e1O3jx9Hjw-X5574PQJSUhJSS9kdKpkBZFEZKIFUdoSklBgoiS-BhNSU8EUUFfJ-jM-w9CKI3T4hRNhmga02yK3pZgbKMVXrutMPpbtNoaLEyJn2Hb1eMq9_hOQyvcHi9Ei22F23fAG6Nst6u12eInZ1vQBrPfZIT7UvDn6KQStYeLw5yhzeL-Zf4QrNbLx_ntKlAso20ggVVRUuWQJLI_W1ZEpEleyjLO4gRUJFQiYpELljKQJMloXjJWMAlxSUiSp2yGrsfenbOfHfiWN9orqGthwHae0z5CKRvAcASVs947qPjO6ab_ilPCByV8sMkHm3yw2QeuDs2dbKD8g4_6eiAfAej_-9LguFcajIJSO1AtL63-r_sHLG-C9w</recordid><startdate>19990305</startdate><enddate>19990305</enddate><creator>Gong, Da-Wei</creator><creator>He, Yufang</creator><creator>Reitman, Marc L.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>19990305</creationdate><title>Genomic Organization and Regulation by Dietary Fat of the Uncoupling Protein 3 and 2 Genes</title><author>Gong, Da-Wei ; He, Yufang ; Reitman, Marc L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c371t-be3f25f8e55b104bf0a658dbd4745ec2ac5a4a8a363eb05718d3393be4d005863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Adipose Tissue - metabolism</topic><topic>Alternative Splicing</topic><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Carrier Proteins - genetics</topic><topic>Cloning, Molecular</topic><topic>diet induced obesity</topic><topic>Dietary Fats - administration & dosage</topic><topic>Dietary Fats - pharmacology</topic><topic>Disease Susceptibility</topic><topic>Exons - genetics</topic><topic>Gene Expression Regulation</topic><topic>Humans</topic><topic>Ion Channels</topic><topic>Membrane Transport Proteins</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Mitochondrial Proteins</topic><topic>Molecular Sequence Data</topic><topic>Muscle, Skeletal - metabolism</topic><topic>Obesity - chemically induced</topic><topic>Obesity - genetics</topic><topic>Polymerase Chain Reaction</topic><topic>Protein Isoforms - genetics</topic><topic>Proteins - genetics</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Sequence Homology, Amino Acid</topic><topic>thermogenesis</topic><topic>Uncoupling Protein 2</topic><topic>Uncoupling Protein 3</topic><topic>uncoupling proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gong, Da-Wei</creatorcontrib><creatorcontrib>He, Yufang</creatorcontrib><creatorcontrib>Reitman, Marc L.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gong, Da-Wei</au><au>He, Yufang</au><au>Reitman, Marc L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genomic Organization and Regulation by Dietary Fat of the Uncoupling Protein 3 and 2 Genes</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>1999-03-05</date><risdate>1999</risdate><volume>256</volume><issue>1</issue><spage>27</spage><epage>32</epage><pages>27-32</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>Uncoupling protein-1 (UCP1) dissipates the transmitochondrial proton gradient as heat. UCP2 and UCP3 are two recently discovered homologues that also have uncoupling activity and thus presumably have a role in energy homeostasis. We now report the genomic structure of murine UCP3 (7 exons) and UCP2 (8 exons). UCP3 is ∼8 kilobases upstream of UCP2. An UCP3 variant mRNA, UCP3S, was also found and characterized. The effect of a high fat diet (45% versus 10%) on UCP3 and UCP2 mRNA levels was measured. Eating the 45% fat diet for eight weeks caused greater weight gain in AKR and C57BL/6J mice than in the obesity-resistant A/J mice. The high fat diet increased muscle UCP3 expression twofold in C57BL/6J animals. UCP2 expression increased slightly on the 45% fat diet in white adipose of AKR mice, but not in A/J or C57BL/6J mice. In skeletal muscle, UCP2 expression showed little variation with diet. Thus, UCP2 and UCP3 expression levels change in response to diet-induced obesity, but the changes are modest and depend on the tissue and genotype. The data suggest that it is not a reduction in UCP2 or UCP3 expression that causes obesity in the susceptible mice.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>10066417</pmid><doi>10.1006/bbrc.1999.0239</doi><tpages>6</tpages></addata></record> |
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subjects | Adipose Tissue - metabolism Alternative Splicing Amino Acid Sequence Animals Carrier Proteins - genetics Cloning, Molecular diet induced obesity Dietary Fats - administration & dosage Dietary Fats - pharmacology Disease Susceptibility Exons - genetics Gene Expression Regulation Humans Ion Channels Membrane Transport Proteins Mice Mice, Inbred Strains Mitochondrial Proteins Molecular Sequence Data Muscle, Skeletal - metabolism Obesity - chemically induced Obesity - genetics Polymerase Chain Reaction Protein Isoforms - genetics Proteins - genetics RNA, Messenger - genetics RNA, Messenger - metabolism Sequence Homology, Amino Acid thermogenesis Uncoupling Protein 2 Uncoupling Protein 3 uncoupling proteins |
title | Genomic Organization and Regulation by Dietary Fat of the Uncoupling Protein 3 and 2 Genes |
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