Molecular cloning and expression analysis of the GNAS gene in pig and porcine fibroblast cells
The Alpha subunit of the stimulatory guanine nucleotide-binding protein (GNAS) is a complex imprinted gene. The major product of the GNAS gene is the α-subunit of the guanine nucleotide-binding protein (Gas), which plays a key role in multiple signal transduction pathways. Gas is required for the pr...
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description | The Alpha subunit of the stimulatory guanine nucleotide-binding protein (GNAS) is a complex imprinted gene. The major product of the GNAS gene is the α-subunit of the guanine nucleotide-binding protein (Gas), which plays a key role in multiple signal transduction pathways. Gas is required for the production of the receptor-stimulated intracellular cyclic adenosine monophosphate (cAMP). It has been demonstrated that an increase in the concentration of the intracellular second messenger cAMP promotes apoptosis in different tumor entities. Mutations of GNAS have also been identified in many tumors. This study aimed to investigate the expression pattern and the apoptosis effect in fibroblast cells for porcine GNAS. The results show that GNAS mRNA was detected in a wide range of tissues, especially in the longissimus dorsi muscle and thyroid gland. The developmental pattern of GNAS mRNA in the thyroid gland of Jinhua pigs was then examined; however, there was no significant difference (P > 0.05) among any of the stages. GNAS gene expression was relatively stable in the thyroid gland during the entire growth and development process. The developmental pattern of GNAS mRNA in the longissimus dorsi muscle was significantly different among the various developmental stages (P < 0.01). GNAS mRNA was strongly expressed at 60 days, 90 days, and 150 days after birth, whereas the expression level was very low during the embryo stages. Target RNA interference of GNAS in porcine fibroblast cells leads to lower mRNA expression of Bcl-2, Fas, and Caspase-3, which are recognized as apoptosis related markers. |
doi_str_mv | 10.4238/2014.July.24.26 |
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The major product of the GNAS gene is the α-subunit of the guanine nucleotide-binding protein (Gas), which plays a key role in multiple signal transduction pathways. Gas is required for the production of the receptor-stimulated intracellular cyclic adenosine monophosphate (cAMP). It has been demonstrated that an increase in the concentration of the intracellular second messenger cAMP promotes apoptosis in different tumor entities. Mutations of GNAS have also been identified in many tumors. This study aimed to investigate the expression pattern and the apoptosis effect in fibroblast cells for porcine GNAS. The results show that GNAS mRNA was detected in a wide range of tissues, especially in the longissimus dorsi muscle and thyroid gland. The developmental pattern of GNAS mRNA in the thyroid gland of Jinhua pigs was then examined; however, there was no significant difference (P > 0.05) among any of the stages. GNAS gene expression was relatively stable in the thyroid gland during the entire growth and development process. The developmental pattern of GNAS mRNA in the longissimus dorsi muscle was significantly different among the various developmental stages (P < 0.01). GNAS mRNA was strongly expressed at 60 days, 90 days, and 150 days after birth, whereas the expression level was very low during the embryo stages. Target RNA interference of GNAS in porcine fibroblast cells leads to lower mRNA expression of Bcl-2, Fas, and Caspase-3, which are recognized as apoptosis related markers.</description><identifier>ISSN: 1676-5680</identifier><identifier>EISSN: 1676-5680</identifier><identifier>DOI: 10.4238/2014.July.24.26</identifier><identifier>PMID: 25078603</identifier><language>eng</language><publisher>Brazil</publisher><subject>Age Factors ; Animals ; Apoptosis - genetics ; Caspase 3 - genetics ; Caspase 3 - metabolism ; Cloning, Molecular ; Embryo, Mammalian ; fas Receptor - genetics ; fas Receptor - metabolism ; Fibroblasts - cytology ; Fibroblasts - metabolism ; Gene Expression Regulation, Developmental ; GTP-Binding Protein alpha Subunits, Gs - antagonists & inhibitors ; GTP-Binding Protein alpha Subunits, Gs - classification ; GTP-Binding Protein alpha Subunits, Gs - genetics ; GTP-Binding Protein alpha Subunits, Gs - metabolism ; Muscle, Skeletal - growth & development ; Muscle, Skeletal - metabolism ; Organ Specificity ; Phylogeny ; Proto-Oncogene Proteins c-bcl-2 - genetics ; Proto-Oncogene Proteins c-bcl-2 - metabolism ; RNA, Messenger - antagonists & inhibitors ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; RNA, Small Interfering - genetics ; RNA, Small Interfering - metabolism ; Sequence Homology, Amino Acid ; Swine ; Thyroid Gland - growth & development ; Thyroid Gland - metabolism</subject><ispartof>Genetics and molecular research, 2014-07, Vol.13 (3), p.5463-5473</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c338t-3c7bef34d7d12d49f66a338f954e2f9827aae9d119875d07a824b976979b56c13</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25078603$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Peng, J</creatorcontrib><creatorcontrib>Li, Y L</creatorcontrib><creatorcontrib>Shen, Y F</creatorcontrib><creatorcontrib>Wang, Y</creatorcontrib><creatorcontrib>Xu, N Y</creatorcontrib><title>Molecular cloning and expression analysis of the GNAS gene in pig and porcine fibroblast cells</title><title>Genetics and molecular research</title><addtitle>Genet Mol Res</addtitle><description>The Alpha subunit of the stimulatory guanine nucleotide-binding protein (GNAS) is a complex imprinted gene. The major product of the GNAS gene is the α-subunit of the guanine nucleotide-binding protein (Gas), which plays a key role in multiple signal transduction pathways. Gas is required for the production of the receptor-stimulated intracellular cyclic adenosine monophosphate (cAMP). It has been demonstrated that an increase in the concentration of the intracellular second messenger cAMP promotes apoptosis in different tumor entities. Mutations of GNAS have also been identified in many tumors. This study aimed to investigate the expression pattern and the apoptosis effect in fibroblast cells for porcine GNAS. The results show that GNAS mRNA was detected in a wide range of tissues, especially in the longissimus dorsi muscle and thyroid gland. The developmental pattern of GNAS mRNA in the thyroid gland of Jinhua pigs was then examined; however, there was no significant difference (P > 0.05) among any of the stages. GNAS gene expression was relatively stable in the thyroid gland during the entire growth and development process. The developmental pattern of GNAS mRNA in the longissimus dorsi muscle was significantly different among the various developmental stages (P < 0.01). GNAS mRNA was strongly expressed at 60 days, 90 days, and 150 days after birth, whereas the expression level was very low during the embryo stages. Target RNA interference of GNAS in porcine fibroblast cells leads to lower mRNA expression of Bcl-2, Fas, and Caspase-3, which are recognized as apoptosis related markers.</description><subject>Age Factors</subject><subject>Animals</subject><subject>Apoptosis - genetics</subject><subject>Caspase 3 - genetics</subject><subject>Caspase 3 - metabolism</subject><subject>Cloning, Molecular</subject><subject>Embryo, Mammalian</subject><subject>fas Receptor - genetics</subject><subject>fas Receptor - metabolism</subject><subject>Fibroblasts - cytology</subject><subject>Fibroblasts - metabolism</subject><subject>Gene Expression Regulation, Developmental</subject><subject>GTP-Binding Protein alpha Subunits, Gs - antagonists & inhibitors</subject><subject>GTP-Binding Protein alpha Subunits, Gs - classification</subject><subject>GTP-Binding Protein alpha Subunits, Gs - genetics</subject><subject>GTP-Binding Protein alpha Subunits, Gs - metabolism</subject><subject>Muscle, Skeletal - growth & development</subject><subject>Muscle, Skeletal - metabolism</subject><subject>Organ Specificity</subject><subject>Phylogeny</subject><subject>Proto-Oncogene Proteins c-bcl-2 - genetics</subject><subject>Proto-Oncogene Proteins c-bcl-2 - metabolism</subject><subject>RNA, Messenger - antagonists & inhibitors</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>RNA, Small Interfering - genetics</subject><subject>RNA, Small Interfering - metabolism</subject><subject>Sequence Homology, Amino Acid</subject><subject>Swine</subject><subject>Thyroid Gland - growth & development</subject><subject>Thyroid Gland - metabolism</subject><issn>1676-5680</issn><issn>1676-5680</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkMFPwyAUh4nRuDk9ezMcvbQDSoEel0WnZupBvUpoCxPDSoU2cf-9bTaNJx7vfe-Xlw-AS4xSSjIxJwjT9KF3u5TQlLAjMMWMsyRnAh3_qyfgLMZPhEhOBToFE5IjLhjKpuD90Ttd9U4FWDnf2GYDVVND_d0GHaP1zfBVbhdthN7A7kPD1dPiBW50o6FtYGv3fOtDZYeWsWXwpVOxg5V2Lp6DE6Nc1BeHdwbebm9el3fJ-nl1v1yskyrLRJdkFS-1yWjNa0xqWhjG1DAwRU41MYUgXCld1BgXguc14koQWhacFbwoc1bhbAau97lt8F-9jp3c2jheoBrt-yhxnmNE0JA0oPM9WgUfY9BGtsFuVdhJjOQoVY5S5ShVEioJGzauDuF9udX1H_9rMfsBPAZy0w</recordid><startdate>20140724</startdate><enddate>20140724</enddate><creator>Peng, J</creator><creator>Li, Y L</creator><creator>Shen, Y F</creator><creator>Wang, Y</creator><creator>Xu, N Y</creator><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>7X8</scope></search><sort><creationdate>20140724</creationdate><title>Molecular cloning and expression analysis of the GNAS gene in pig and porcine fibroblast cells</title><author>Peng, J ; Li, Y L ; Shen, Y F ; Wang, Y ; Xu, N Y</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c338t-3c7bef34d7d12d49f66a338f954e2f9827aae9d119875d07a824b976979b56c13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Age Factors</topic><topic>Animals</topic><topic>Apoptosis - genetics</topic><topic>Caspase 3 - genetics</topic><topic>Caspase 3 - metabolism</topic><topic>Cloning, Molecular</topic><topic>Embryo, Mammalian</topic><topic>fas Receptor - genetics</topic><topic>fas Receptor - metabolism</topic><topic>Fibroblasts - cytology</topic><topic>Fibroblasts - metabolism</topic><topic>Gene Expression Regulation, Developmental</topic><topic>GTP-Binding Protein alpha Subunits, Gs - antagonists & inhibitors</topic><topic>GTP-Binding Protein alpha Subunits, Gs - classification</topic><topic>GTP-Binding Protein alpha Subunits, Gs - genetics</topic><topic>GTP-Binding Protein alpha Subunits, Gs - metabolism</topic><topic>Muscle, Skeletal - growth & development</topic><topic>Muscle, Skeletal - metabolism</topic><topic>Organ Specificity</topic><topic>Phylogeny</topic><topic>Proto-Oncogene Proteins c-bcl-2 - genetics</topic><topic>Proto-Oncogene Proteins c-bcl-2 - metabolism</topic><topic>RNA, Messenger - antagonists & inhibitors</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>RNA, Small Interfering - genetics</topic><topic>RNA, Small Interfering - metabolism</topic><topic>Sequence Homology, Amino Acid</topic><topic>Swine</topic><topic>Thyroid Gland - growth & development</topic><topic>Thyroid Gland - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Peng, J</creatorcontrib><creatorcontrib>Li, Y L</creatorcontrib><creatorcontrib>Shen, Y F</creatorcontrib><creatorcontrib>Wang, Y</creatorcontrib><creatorcontrib>Xu, N Y</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Genetics and molecular research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Peng, J</au><au>Li, Y L</au><au>Shen, Y F</au><au>Wang, Y</au><au>Xu, N Y</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular cloning and expression analysis of the GNAS gene in pig and porcine fibroblast cells</atitle><jtitle>Genetics and molecular research</jtitle><addtitle>Genet Mol Res</addtitle><date>2014-07-24</date><risdate>2014</risdate><volume>13</volume><issue>3</issue><spage>5463</spage><epage>5473</epage><pages>5463-5473</pages><issn>1676-5680</issn><eissn>1676-5680</eissn><abstract>The Alpha subunit of the stimulatory guanine nucleotide-binding protein (GNAS) is a complex imprinted gene. The major product of the GNAS gene is the α-subunit of the guanine nucleotide-binding protein (Gas), which plays a key role in multiple signal transduction pathways. Gas is required for the production of the receptor-stimulated intracellular cyclic adenosine monophosphate (cAMP). It has been demonstrated that an increase in the concentration of the intracellular second messenger cAMP promotes apoptosis in different tumor entities. Mutations of GNAS have also been identified in many tumors. This study aimed to investigate the expression pattern and the apoptosis effect in fibroblast cells for porcine GNAS. The results show that GNAS mRNA was detected in a wide range of tissues, especially in the longissimus dorsi muscle and thyroid gland. The developmental pattern of GNAS mRNA in the thyroid gland of Jinhua pigs was then examined; however, there was no significant difference (P > 0.05) among any of the stages. GNAS gene expression was relatively stable in the thyroid gland during the entire growth and development process. The developmental pattern of GNAS mRNA in the longissimus dorsi muscle was significantly different among the various developmental stages (P < 0.01). GNAS mRNA was strongly expressed at 60 days, 90 days, and 150 days after birth, whereas the expression level was very low during the embryo stages. Target RNA interference of GNAS in porcine fibroblast cells leads to lower mRNA expression of Bcl-2, Fas, and Caspase-3, which are recognized as apoptosis related markers.</abstract><cop>Brazil</cop><pmid>25078603</pmid><doi>10.4238/2014.July.24.26</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Age Factors Animals Apoptosis - genetics Caspase 3 - genetics Caspase 3 - metabolism Cloning, Molecular Embryo, Mammalian fas Receptor - genetics fas Receptor - metabolism Fibroblasts - cytology Fibroblasts - metabolism Gene Expression Regulation, Developmental GTP-Binding Protein alpha Subunits, Gs - antagonists & inhibitors GTP-Binding Protein alpha Subunits, Gs - classification GTP-Binding Protein alpha Subunits, Gs - genetics GTP-Binding Protein alpha Subunits, Gs - metabolism Muscle, Skeletal - growth & development Muscle, Skeletal - metabolism Organ Specificity Phylogeny Proto-Oncogene Proteins c-bcl-2 - genetics Proto-Oncogene Proteins c-bcl-2 - metabolism RNA, Messenger - antagonists & inhibitors RNA, Messenger - genetics RNA, Messenger - metabolism RNA, Small Interfering - genetics RNA, Small Interfering - metabolism Sequence Homology, Amino Acid Swine Thyroid Gland - growth & development Thyroid Gland - metabolism |
title | Molecular cloning and expression analysis of the GNAS gene in pig and porcine fibroblast cells |
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