Function and Transcriptional Regulation of Bovine TORC2 Gene in Adipocytes: Roles of C/EBPγ, XBP1, INSM1 and ZNF263
The TORC2 gene is a member of the transducer of the regulated cyclic adenosine monophosphate (cAMP) response element binding protein gene family, which plays a key role in metabolism and adipogenesis. In the present study, we confirmed the role of TORC2 in bovine preadipocyte proliferation through c...
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description | The TORC2 gene is a member of the transducer of the regulated cyclic adenosine monophosphate (cAMP) response element binding protein gene family, which plays a key role in metabolism and adipogenesis. In the present study, we confirmed the role of TORC2 in bovine preadipocyte proliferation through cell cycle staining flow cytometry, cell counting assay, 5-ethynyl-2′-deoxyuridine staining (EdU), and mRNA and protein expression analysis of proliferation-related marker genes. In addition, Oil red O staining analysis, immunofluorescence of adiponectin, mRNA and protein level expression of lipid related marker genes confirmed the role of TORC2 in the regulation of bovine adipocyte differentiation. Furthermore, the transcription start site and sub-cellular localization of the TORC2 gene was identified in bovine adipocytes. To investigate the underlying regulatory mechanism of the bovine TORC2, we cloned a 1990 bp of the 5’ untranslated region (5′UTR) promoter region into a luciferase reporter vector and seven vector fragments were constructed through serial deletion of the 5′UTR flanking region. The core promoter region of the TORC2 gene was identified at location −314 to −69 bp upstream of the transcription start site. Based on the results of the transcriptional activities of the promoter vector fragments, luciferase activities of mutated fragments and siRNAs interference, four transcription factors (CCAAT/enhancer-binding protein C/BEPγ, X-box binding protein 1 XBP1, Insulinoma-associated 1 INSM1, and Zinc finger protein 263 ZNF263) were identified as the transcriptional regulators of TORC2 gene. These findings were further confirmed through Electrophoretic Mobility Shift Assay (EMSA) within nuclear extracts of bovine adipocytes. Furthermore, we also identified that C/EBPγ, XBP1, INSM1 and ZNF263 regulate TORC2 gene as activators in the promoter region. We can conclude that TORC2 gene is potentially a positive regulator of adipogenesis. These findings will not only provide an insight for the improvement of intramuscular fat in cattle, but will enhance our understanding regarding therapeutic intervention of metabolic syndrome and obesity in public health as well. |
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In the present study, we confirmed the role of TORC2 in bovine preadipocyte proliferation through cell cycle staining flow cytometry, cell counting assay, 5-ethynyl-2′-deoxyuridine staining (EdU), and mRNA and protein expression analysis of proliferation-related marker genes. In addition, Oil red O staining analysis, immunofluorescence of adiponectin, mRNA and protein level expression of lipid related marker genes confirmed the role of TORC2 in the regulation of bovine adipocyte differentiation. Furthermore, the transcription start site and sub-cellular localization of the TORC2 gene was identified in bovine adipocytes. To investigate the underlying regulatory mechanism of the bovine TORC2, we cloned a 1990 bp of the 5’ untranslated region (5′UTR) promoter region into a luciferase reporter vector and seven vector fragments were constructed through serial deletion of the 5′UTR flanking region. The core promoter region of the TORC2 gene was identified at location −314 to −69 bp upstream of the transcription start site. Based on the results of the transcriptional activities of the promoter vector fragments, luciferase activities of mutated fragments and siRNAs interference, four transcription factors (CCAAT/enhancer-binding protein C/BEPγ, X-box binding protein 1 XBP1, Insulinoma-associated 1 INSM1, and Zinc finger protein 263 ZNF263) were identified as the transcriptional regulators of TORC2 gene. These findings were further confirmed through Electrophoretic Mobility Shift Assay (EMSA) within nuclear extracts of bovine adipocytes. Furthermore, we also identified that C/EBPγ, XBP1, INSM1 and ZNF263 regulate TORC2 gene as activators in the promoter region. We can conclude that TORC2 gene is potentially a positive regulator of adipogenesis. These findings will not only provide an insight for the improvement of intramuscular fat in cattle, but will enhance our understanding regarding therapeutic intervention of metabolic syndrome and obesity in public health as well.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms20184338</identifier><identifier>PMID: 31487963</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>1-Phosphatidylinositol 3-kinase ; Adenosine kinase ; Adenosine monophosphate ; Adipocytes ; Adipogenesis ; AKT protein ; Cattle ; Cell cycle ; Cyclic AMP response element-binding protein ; Enzymes ; Gene expression ; Gene regulation ; Genes ; Glucagon ; Glucocorticoids ; Gluconeogenesis ; Insulin ; Insulin resistance ; Kinases ; Meat ; Meat industry ; Meat quality ; Metabolism ; Metabolites ; Molecular modelling ; Myogenesis ; Protein kinase ; Proteins ; Transcription</subject><ispartof>International journal of molecular sciences, 2019-09, Vol.20 (18), p.4338</ispartof><rights>2019. This work is licensed under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2019 by the authors. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c286t-a47e01901123af0e9fcb4e793911566e96cb379b1706ecf4bfe9b89aed90a1983</citedby><cites>FETCH-LOGICAL-c286t-a47e01901123af0e9fcb4e793911566e96cb379b1706ecf4bfe9b89aed90a1983</cites><orcidid>0000-0001-5191-3457 ; 0000-0003-3663-7129 ; 0000-0002-0961-1911</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6769628/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6769628/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids></links><search><creatorcontrib>Khan, Rajwali</creatorcontrib><creatorcontrib>Raza, Sayed Haidar Abbas</creatorcontrib><creatorcontrib>Junjvlieke, Zainaguli</creatorcontrib><creatorcontrib>Xiaoyu, Wang</creatorcontrib><creatorcontrib>Garcia, Matthew</creatorcontrib><creatorcontrib>Elnour, Ibrahim Elsaeid</creatorcontrib><creatorcontrib>Hongbao, Wang</creatorcontrib><creatorcontrib>Linsen, Zan</creatorcontrib><title>Function and Transcriptional Regulation of Bovine TORC2 Gene in Adipocytes: Roles of C/EBPγ, XBP1, INSM1 and ZNF263</title><title>International journal of molecular sciences</title><description>The TORC2 gene is a member of the transducer of the regulated cyclic adenosine monophosphate (cAMP) response element binding protein gene family, which plays a key role in metabolism and adipogenesis. In the present study, we confirmed the role of TORC2 in bovine preadipocyte proliferation through cell cycle staining flow cytometry, cell counting assay, 5-ethynyl-2′-deoxyuridine staining (EdU), and mRNA and protein expression analysis of proliferation-related marker genes. In addition, Oil red O staining analysis, immunofluorescence of adiponectin, mRNA and protein level expression of lipid related marker genes confirmed the role of TORC2 in the regulation of bovine adipocyte differentiation. Furthermore, the transcription start site and sub-cellular localization of the TORC2 gene was identified in bovine adipocytes. To investigate the underlying regulatory mechanism of the bovine TORC2, we cloned a 1990 bp of the 5’ untranslated region (5′UTR) promoter region into a luciferase reporter vector and seven vector fragments were constructed through serial deletion of the 5′UTR flanking region. The core promoter region of the TORC2 gene was identified at location −314 to −69 bp upstream of the transcription start site. Based on the results of the transcriptional activities of the promoter vector fragments, luciferase activities of mutated fragments and siRNAs interference, four transcription factors (CCAAT/enhancer-binding protein C/BEPγ, X-box binding protein 1 XBP1, Insulinoma-associated 1 INSM1, and Zinc finger protein 263 ZNF263) were identified as the transcriptional regulators of TORC2 gene. These findings were further confirmed through Electrophoretic Mobility Shift Assay (EMSA) within nuclear extracts of bovine adipocytes. Furthermore, we also identified that C/EBPγ, XBP1, INSM1 and ZNF263 regulate TORC2 gene as activators in the promoter region. We can conclude that TORC2 gene is potentially a positive regulator of adipogenesis. These findings will not only provide an insight for the improvement of intramuscular fat in cattle, but will enhance our understanding regarding therapeutic intervention of metabolic syndrome and obesity in public health as well.</description><subject>1-Phosphatidylinositol 3-kinase</subject><subject>Adenosine kinase</subject><subject>Adenosine monophosphate</subject><subject>Adipocytes</subject><subject>Adipogenesis</subject><subject>AKT protein</subject><subject>Cattle</subject><subject>Cell cycle</subject><subject>Cyclic AMP response element-binding protein</subject><subject>Enzymes</subject><subject>Gene expression</subject><subject>Gene regulation</subject><subject>Genes</subject><subject>Glucagon</subject><subject>Glucocorticoids</subject><subject>Gluconeogenesis</subject><subject>Insulin</subject><subject>Insulin resistance</subject><subject>Kinases</subject><subject>Meat</subject><subject>Meat industry</subject><subject>Meat quality</subject><subject>Metabolism</subject><subject>Metabolites</subject><subject>Molecular modelling</subject><subject>Myogenesis</subject><subject>Protein kinase</subject><subject>Proteins</subject><subject>Transcription</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpVUdtKAzEUDKJ4f_MDAr52NbfNbnwQbGlV8EatIL6EbHpWU7abmuwW_C7_w2-yqyL6dIYzwwzMIHRAyRHnihy72TwyQnPBeb6GtqlgLCFEZut_8BbaiXFGCOMsVZtoi1ORZ0rybdSM2to2ztfY1FM8CaaONrhF9zEVHsNzW5kv2pe475euBjy5HQ8YPocVdDU-m7qFt28NxBM89hXETjk4HvbvPt57-LF_R3v48ub-mn4FPN2MmOR7aKM0VYT9n7uLHkbDyeAiubo9vxycXSWW5bJJjMiAUEUoZdyUBFRpCwGZ4orSVEpQ0hY8UwXNiARbiqIEVeTKwFQRQ1XOd9Hpt--iLeYwtVA3wVR6EdzchDftjdP_mdq96Ge_1DKTSrLO4PDHIPjXFmKjZ74Nq2aiZlxIIVKS0pWq962ywccYoPxNoER3G-m_G_FPIWSCEg</recordid><startdate>20190904</startdate><enddate>20190904</enddate><creator>Khan, Rajwali</creator><creator>Raza, Sayed Haidar Abbas</creator><creator>Junjvlieke, Zainaguli</creator><creator>Xiaoyu, Wang</creator><creator>Garcia, Matthew</creator><creator>Elnour, Ibrahim Elsaeid</creator><creator>Hongbao, Wang</creator><creator>Linsen, Zan</creator><general>MDPI AG</general><general>MDPI</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-5191-3457</orcidid><orcidid>https://orcid.org/0000-0003-3663-7129</orcidid><orcidid>https://orcid.org/0000-0002-0961-1911</orcidid></search><sort><creationdate>20190904</creationdate><title>Function and Transcriptional Regulation of Bovine TORC2 Gene in Adipocytes: Roles of C/EBPγ, XBP1, INSM1 and ZNF263</title><author>Khan, Rajwali ; 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In the present study, we confirmed the role of TORC2 in bovine preadipocyte proliferation through cell cycle staining flow cytometry, cell counting assay, 5-ethynyl-2′-deoxyuridine staining (EdU), and mRNA and protein expression analysis of proliferation-related marker genes. In addition, Oil red O staining analysis, immunofluorescence of adiponectin, mRNA and protein level expression of lipid related marker genes confirmed the role of TORC2 in the regulation of bovine adipocyte differentiation. Furthermore, the transcription start site and sub-cellular localization of the TORC2 gene was identified in bovine adipocytes. To investigate the underlying regulatory mechanism of the bovine TORC2, we cloned a 1990 bp of the 5’ untranslated region (5′UTR) promoter region into a luciferase reporter vector and seven vector fragments were constructed through serial deletion of the 5′UTR flanking region. The core promoter region of the TORC2 gene was identified at location −314 to −69 bp upstream of the transcription start site. Based on the results of the transcriptional activities of the promoter vector fragments, luciferase activities of mutated fragments and siRNAs interference, four transcription factors (CCAAT/enhancer-binding protein C/BEPγ, X-box binding protein 1 XBP1, Insulinoma-associated 1 INSM1, and Zinc finger protein 263 ZNF263) were identified as the transcriptional regulators of TORC2 gene. These findings were further confirmed through Electrophoretic Mobility Shift Assay (EMSA) within nuclear extracts of bovine adipocytes. Furthermore, we also identified that C/EBPγ, XBP1, INSM1 and ZNF263 regulate TORC2 gene as activators in the promoter region. We can conclude that TORC2 gene is potentially a positive regulator of adipogenesis. These findings will not only provide an insight for the improvement of intramuscular fat in cattle, but will enhance our understanding regarding therapeutic intervention of metabolic syndrome and obesity in public health as well.</abstract><cop>Basel</cop><pub>MDPI AG</pub><pmid>31487963</pmid><doi>10.3390/ijms20184338</doi><orcidid>https://orcid.org/0000-0001-5191-3457</orcidid><orcidid>https://orcid.org/0000-0003-3663-7129</orcidid><orcidid>https://orcid.org/0000-0002-0961-1911</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 1-Phosphatidylinositol 3-kinase Adenosine kinase Adenosine monophosphate Adipocytes Adipogenesis AKT protein Cattle Cell cycle Cyclic AMP response element-binding protein Enzymes Gene expression Gene regulation Genes Glucagon Glucocorticoids Gluconeogenesis Insulin Insulin resistance Kinases Meat Meat industry Meat quality Metabolism Metabolites Molecular modelling Myogenesis Protein kinase Proteins Transcription |
title | Function and Transcriptional Regulation of Bovine TORC2 Gene in Adipocytes: Roles of C/EBPγ, XBP1, INSM1 and ZNF263 |
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