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Molecular cloning, tissue distribution and ontogenetic expression of Xiang pig Chemerin and its involvement in regulating energy metabolism through Akt and ERK1/2 signaling pathways
Chemerin, as a new member of adipokines family, is highly expressed in adipose tissue in rodent and its expression increases with obesity. Moreover, chemerin has been reported to have significant relationship with metabolic syndrome and insulin sensitivity. Here, the gene encoding chemerin from Xian...
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Published in: | Molecular biology reports 2012-02, Vol.39 (2), p.1887-1894 |
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creator | Yang, Huansheng Li, Fengna Kong, Xiangfeng Yuan, Xiaoxue Lian, Guoqi Geng, Meimei Li, Tiejun Yin, Jingdong Yin, Yulong |
description | Chemerin, as a new member of adipokines family, is highly expressed in adipose tissue in rodent and its expression increases with obesity. Moreover, chemerin has been reported to have significant relationship with metabolic syndrome and insulin sensitivity. Here, the gene encoding chemerin from Xiang pig was cloned. The open reading frame of this cDNA encodes 163 deduced amino acid residues. The putative protein has a N-terminal signaling peptide and a nuclear localization signal profile which are highly conserved among the vertebrate orthologs. Both chemerin and chemerinR are highly expressed in lung, kidney and small intestine in adult Xiang pig. Besides these tissues, chemerin is abundant in liver and backfat, and chemerinR is abundant in spleen and skeletal muscle. We also investigated the age-dependent expression of chemerin in suckling Xiang piglets in various tissues, which showed an interaction between age and segments in abundance of chemerin and chemerinR from day 1 to day 21. For chemerinR, it was abundant in skeletal muscle of both adult and fetal Xiang pig. Further, we treated differentiated C2C12 cells with chemerin. The result showed that chemerin regulated energy metabolism partly through Akt and ERK1/2 signaling pathway. Taken together, our findings provide basic molecular information for the deeper investigation on the function of chemerin. |
doi_str_mv | 10.1007/s11033-011-0934-8 |
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Moreover, chemerin has been reported to have significant relationship with metabolic syndrome and insulin sensitivity. Here, the gene encoding chemerin from Xiang pig was cloned. The open reading frame of this cDNA encodes 163 deduced amino acid residues. The putative protein has a N-terminal signaling peptide and a nuclear localization signal profile which are highly conserved among the vertebrate orthologs. Both chemerin and chemerinR are highly expressed in lung, kidney and small intestine in adult Xiang pig. Besides these tissues, chemerin is abundant in liver and backfat, and chemerinR is abundant in spleen and skeletal muscle. We also investigated the age-dependent expression of chemerin in suckling Xiang piglets in various tissues, which showed an interaction between age and segments in abundance of chemerin and chemerinR from day 1 to day 21. For chemerinR, it was abundant in skeletal muscle of both adult and fetal Xiang pig. Further, we treated differentiated C2C12 cells with chemerin. The result showed that chemerin regulated energy metabolism partly through Akt and ERK1/2 signaling pathway. Taken together, our findings provide basic molecular information for the deeper investigation on the function of chemerin.</description><identifier>ISSN: 0301-4851</identifier><identifier>EISSN: 1573-4978</identifier><identifier>DOI: 10.1007/s11033-011-0934-8</identifier><identifier>PMID: 21643960</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Adipokines - genetics ; Adipokines - metabolism ; Adipokines - pharmacology ; Age Factors ; Amino acids ; Analysis of Variance ; Animal Anatomy ; Animal Biochemistry ; Animals ; Bioenergetics ; Biomedical and Life Sciences ; Blotting, Western ; Cell Line, Tumor ; Chemotactic Factors - genetics ; Chemotactic Factors - metabolism ; Cloning ; Cloning, Molecular ; Computational Biology ; Energy Metabolism - drug effects ; Energy Metabolism - physiology ; Gene Expression ; Gene Expression Profiling ; Histology ; Insulin ; Kidney ; Kinases ; Life Sciences ; Lung ; MAP Kinase Signaling System - physiology ; metabolic disorders ; Metabolism ; Mice ; Molecular biology ; Morphology ; Muscles ; obesity ; Open Reading Frames - genetics ; Reverse Transcriptase Polymerase Chain Reaction ; rodents ; Signal transduction ; Sus scrofa - genetics</subject><ispartof>Molecular biology reports, 2012-02, Vol.39 (2), p.1887-1894</ispartof><rights>Springer Science+Business Media B.V. 2011</rights><rights>Springer Science+Business Media B.V. 2012</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c469t-3a8cf8c8f3b77c859eb9cbdd6b3d3ac287ce239d6a89d8004df1c001737756323</citedby><cites>FETCH-LOGICAL-c469t-3a8cf8c8f3b77c859eb9cbdd6b3d3ac287ce239d6a89d8004df1c001737756323</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21643960$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Huansheng</creatorcontrib><creatorcontrib>Li, Fengna</creatorcontrib><creatorcontrib>Kong, Xiangfeng</creatorcontrib><creatorcontrib>Yuan, Xiaoxue</creatorcontrib><creatorcontrib>Lian, Guoqi</creatorcontrib><creatorcontrib>Geng, Meimei</creatorcontrib><creatorcontrib>Li, Tiejun</creatorcontrib><creatorcontrib>Yin, Jingdong</creatorcontrib><creatorcontrib>Yin, Yulong</creatorcontrib><title>Molecular cloning, tissue distribution and ontogenetic expression of Xiang pig Chemerin and its involvement in regulating energy metabolism through Akt and ERK1/2 signaling pathways</title><title>Molecular biology reports</title><addtitle>Mol Biol Rep</addtitle><addtitle>Mol Biol Rep</addtitle><description>Chemerin, as a new member of adipokines family, is highly expressed in adipose tissue in rodent and its expression increases with obesity. Moreover, chemerin has been reported to have significant relationship with metabolic syndrome and insulin sensitivity. Here, the gene encoding chemerin from Xiang pig was cloned. The open reading frame of this cDNA encodes 163 deduced amino acid residues. The putative protein has a N-terminal signaling peptide and a nuclear localization signal profile which are highly conserved among the vertebrate orthologs. Both chemerin and chemerinR are highly expressed in lung, kidney and small intestine in adult Xiang pig. Besides these tissues, chemerin is abundant in liver and backfat, and chemerinR is abundant in spleen and skeletal muscle. We also investigated the age-dependent expression of chemerin in suckling Xiang piglets in various tissues, which showed an interaction between age and segments in abundance of chemerin and chemerinR from day 1 to day 21. For chemerinR, it was abundant in skeletal muscle of both adult and fetal Xiang pig. Further, we treated differentiated C2C12 cells with chemerin. The result showed that chemerin regulated energy metabolism partly through Akt and ERK1/2 signaling pathway. Taken together, our findings provide basic molecular information for the deeper investigation on the function of chemerin.</description><subject>Adipokines - genetics</subject><subject>Adipokines - metabolism</subject><subject>Adipokines - pharmacology</subject><subject>Age Factors</subject><subject>Amino acids</subject><subject>Analysis of Variance</subject><subject>Animal Anatomy</subject><subject>Animal Biochemistry</subject><subject>Animals</subject><subject>Bioenergetics</subject><subject>Biomedical and Life Sciences</subject><subject>Blotting, Western</subject><subject>Cell Line, Tumor</subject><subject>Chemotactic Factors - genetics</subject><subject>Chemotactic Factors - metabolism</subject><subject>Cloning</subject><subject>Cloning, Molecular</subject><subject>Computational Biology</subject><subject>Energy Metabolism - drug effects</subject><subject>Energy Metabolism - physiology</subject><subject>Gene Expression</subject><subject>Gene Expression Profiling</subject><subject>Histology</subject><subject>Insulin</subject><subject>Kidney</subject><subject>Kinases</subject><subject>Life Sciences</subject><subject>Lung</subject><subject>MAP Kinase Signaling System - physiology</subject><subject>metabolic disorders</subject><subject>Metabolism</subject><subject>Mice</subject><subject>Molecular biology</subject><subject>Morphology</subject><subject>Muscles</subject><subject>obesity</subject><subject>Open Reading Frames - genetics</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>rodents</subject><subject>Signal transduction</subject><subject>Sus scrofa - genetics</subject><issn>0301-4851</issn><issn>1573-4978</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNp9kcFu1DAURS0EokPhA9ggiw0sCLXjJHaW1ahQRBESAold5DgvGZfEnvo5hfkw_q9OU0BCgpUtv3vPld8l5Clnrzlj8gQ5Z0JkjPOM1aLI1D2y4aUUWVFLdZ9smGA8K1TJj8gjxEvGWMFl-ZAc5bwqRF2xDfn5wY9g5lEHakbvrBte0WgRZ6CdxRhsO0frHdWuo95FP4CDaA2FH_sAiMvI9_Sr1W6gezvQ7Q4mCHY12IjUums_XqdHF9OdBhhSWEw5NJHCcKATRN360eJE4y74edjR02_x1n_26T0_ySnawelxsex13H3XB3xMHvR6RHhydx6TL2_OPm_Ps4uPb99tTy8yU1R1zIRWpldG9aKV0qiyhrY2bddVreiENrmSBnJRd5VWdafSdrqeG8a4FFKWlcjFMXmxcvfBX82AsZksGhhH7cDP2NRcyLRRqZLy5X-VqS-lRJmKSdLnf0kv_RzSD295QpSMLzy-ikzwiAH6Zh_spMMhkRaYbNbym1R-s5TfLJ5nd-C5naD77fjVdhLkqwDTyA0Q_iT_m3oDNOu9HQ</recordid><startdate>20120201</startdate><enddate>20120201</enddate><creator>Yang, Huansheng</creator><creator>Li, Fengna</creator><creator>Kong, Xiangfeng</creator><creator>Yuan, Xiaoxue</creator><creator>Lian, Guoqi</creator><creator>Geng, Meimei</creator><creator>Li, Tiejun</creator><creator>Yin, Jingdong</creator><creator>Yin, Yulong</creator><general>Springer Netherlands</general><general>Springer Nature B.V</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>3V.</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>RC3</scope><scope>7ST</scope><scope>C1K</scope><scope>SOI</scope><scope>7X8</scope></search><sort><creationdate>20120201</creationdate><title>Molecular cloning, tissue distribution and ontogenetic expression of Xiang pig Chemerin and its involvement in regulating energy metabolism through Akt and ERK1/2 signaling pathways</title><author>Yang, Huansheng ; Li, Fengna ; Kong, Xiangfeng ; Yuan, Xiaoxue ; Lian, Guoqi ; Geng, Meimei ; Li, Tiejun ; Yin, Jingdong ; Yin, Yulong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c469t-3a8cf8c8f3b77c859eb9cbdd6b3d3ac287ce239d6a89d8004df1c001737756323</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adipokines - genetics</topic><topic>Adipokines - metabolism</topic><topic>Adipokines - pharmacology</topic><topic>Age Factors</topic><topic>Amino acids</topic><topic>Analysis of Variance</topic><topic>Animal Anatomy</topic><topic>Animal Biochemistry</topic><topic>Animals</topic><topic>Bioenergetics</topic><topic>Biomedical and Life Sciences</topic><topic>Blotting, Western</topic><topic>Cell Line, Tumor</topic><topic>Chemotactic Factors - genetics</topic><topic>Chemotactic Factors - metabolism</topic><topic>Cloning</topic><topic>Cloning, Molecular</topic><topic>Computational Biology</topic><topic>Energy Metabolism - drug effects</topic><topic>Energy Metabolism - physiology</topic><topic>Gene Expression</topic><topic>Gene Expression Profiling</topic><topic>Histology</topic><topic>Insulin</topic><topic>Kidney</topic><topic>Kinases</topic><topic>Life Sciences</topic><topic>Lung</topic><topic>MAP Kinase Signaling System - physiology</topic><topic>metabolic disorders</topic><topic>Metabolism</topic><topic>Mice</topic><topic>Molecular biology</topic><topic>Morphology</topic><topic>Muscles</topic><topic>obesity</topic><topic>Open Reading Frames - genetics</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>rodents</topic><topic>Signal transduction</topic><topic>Sus scrofa - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Huansheng</creatorcontrib><creatorcontrib>Li, Fengna</creatorcontrib><creatorcontrib>Kong, Xiangfeng</creatorcontrib><creatorcontrib>Yuan, Xiaoxue</creatorcontrib><creatorcontrib>Lian, Guoqi</creatorcontrib><creatorcontrib>Geng, Meimei</creatorcontrib><creatorcontrib>Li, Tiejun</creatorcontrib><creatorcontrib>Yin, Jingdong</creatorcontrib><creatorcontrib>Yin, Yulong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Science Database (ProQuest)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular biology reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Huansheng</au><au>Li, Fengna</au><au>Kong, Xiangfeng</au><au>Yuan, Xiaoxue</au><au>Lian, Guoqi</au><au>Geng, Meimei</au><au>Li, Tiejun</au><au>Yin, Jingdong</au><au>Yin, Yulong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular cloning, tissue distribution and ontogenetic expression of Xiang pig Chemerin and its involvement in regulating energy metabolism through Akt and ERK1/2 signaling pathways</atitle><jtitle>Molecular biology reports</jtitle><stitle>Mol Biol Rep</stitle><addtitle>Mol Biol Rep</addtitle><date>2012-02-01</date><risdate>2012</risdate><volume>39</volume><issue>2</issue><spage>1887</spage><epage>1894</epage><pages>1887-1894</pages><issn>0301-4851</issn><eissn>1573-4978</eissn><abstract>Chemerin, as a new member of adipokines family, is highly expressed in adipose tissue in rodent and its expression increases with obesity. Moreover, chemerin has been reported to have significant relationship with metabolic syndrome and insulin sensitivity. Here, the gene encoding chemerin from Xiang pig was cloned. The open reading frame of this cDNA encodes 163 deduced amino acid residues. The putative protein has a N-terminal signaling peptide and a nuclear localization signal profile which are highly conserved among the vertebrate orthologs. Both chemerin and chemerinR are highly expressed in lung, kidney and small intestine in adult Xiang pig. Besides these tissues, chemerin is abundant in liver and backfat, and chemerinR is abundant in spleen and skeletal muscle. We also investigated the age-dependent expression of chemerin in suckling Xiang piglets in various tissues, which showed an interaction between age and segments in abundance of chemerin and chemerinR from day 1 to day 21. For chemerinR, it was abundant in skeletal muscle of both adult and fetal Xiang pig. Further, we treated differentiated C2C12 cells with chemerin. The result showed that chemerin regulated energy metabolism partly through Akt and ERK1/2 signaling pathway. Taken together, our findings provide basic molecular information for the deeper investigation on the function of chemerin.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>21643960</pmid><doi>10.1007/s11033-011-0934-8</doi><tpages>8</tpages></addata></record> |
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subjects | Adipokines - genetics Adipokines - metabolism Adipokines - pharmacology Age Factors Amino acids Analysis of Variance Animal Anatomy Animal Biochemistry Animals Bioenergetics Biomedical and Life Sciences Blotting, Western Cell Line, Tumor Chemotactic Factors - genetics Chemotactic Factors - metabolism Cloning Cloning, Molecular Computational Biology Energy Metabolism - drug effects Energy Metabolism - physiology Gene Expression Gene Expression Profiling Histology Insulin Kidney Kinases Life Sciences Lung MAP Kinase Signaling System - physiology metabolic disorders Metabolism Mice Molecular biology Morphology Muscles obesity Open Reading Frames - genetics Reverse Transcriptase Polymerase Chain Reaction rodents Signal transduction Sus scrofa - genetics |
title | Molecular cloning, tissue distribution and ontogenetic expression of Xiang pig Chemerin and its involvement in regulating energy metabolism through Akt and ERK1/2 signaling pathways |
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