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Molecular Cloning, Functional Expression, Pharmacological Characterization and Chromosomal Localization of the Human Metabotropic Glutamate Receptor Type 3
Glutamic acid is the major excitatory amino acid of the central nervous system which interacts with two receptor families, the ionotropic and metabotropic glutamate receptors. The metabotropic glutamate receptors (mGluRs) are coupled to G proteins and can be divided into three subgroups based on the...
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Published in: | Neuropharmacology 1996-05, Vol.35 (5), p.523-530 |
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container_title | Neuropharmacology |
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creator | EMILE, LYDIA MERCKEN, LUC APIOU, FRANCOISE PRADIER, LAURENT BOCK, MARIE-DOMINIQUE MENAGER, JEAN CLOT, JOSETTE DOBLE, ADAM BLANCHARD, JEAN-CHARLES |
description | Glutamic acid is the major excitatory amino acid of the central nervous system which interacts with two receptor families, the ionotropic and metabotropic glutamate receptors. The metabotropic glutamate receptors (mGluRs) are coupled to G proteins and can be divided into three subgroups based on their sequence homology, signal transduction pathway and pharmacology. In this study, we describe the cloning of the cDNA encoding the human metabotropic glutamate receptor type 3 (HmGluR3). It was obtained by reverse transcription-polymerase chain reaction (RT-PCR) with degenerate oligonucleotides corresponding to highly conserved sequences between rat mGluRs. The receptor shows 879 amino acids with 96% amino acid sequence identity with rat mGluR3. It is strongly expressed in fetal and adult whole brain, especially in caudate nucleus and corpus callosum. The gene was identified by fluorescence
in situ hybridization on chromosome 7 band q22. Activation of the human mGluR3, permanently expressed in Baby Hamster Kidney (BHK) cells, by excitatory amino acid inhibits the forskolin-stimulated accumulation of intracellular cAMP. The rank order of potency is
l-glutamic acid ⩾ (1
S,3
R)-1-aminocyclopentane-1,3-dicarboxylic acid ((1
S,3
R)-ACPD) >> ibotenic acid > quisqualic acid. (
RS)-α-methyl-4-carboxyphenylglycine [(
RS)-MCPG, 1 mM] is without effect on inhibition of forskolin-induced cAMP accumulation by
l-glutamic acid. Copyright © 1996 Elsevier Science Ltd. |
doi_str_mv | 10.1016/0028-3908(96)84622-3 |
format | article |
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in situ hybridization on chromosome 7 band q22. Activation of the human mGluR3, permanently expressed in Baby Hamster Kidney (BHK) cells, by excitatory amino acid inhibits the forskolin-stimulated accumulation of intracellular cAMP. The rank order of potency is
l-glutamic acid ⩾ (1
S,3
R)-1-aminocyclopentane-1,3-dicarboxylic acid ((1
S,3
R)-ACPD) >> ibotenic acid > quisqualic acid. (
RS)-α-methyl-4-carboxyphenylglycine [(
RS)-MCPG, 1 mM] is without effect on inhibition of forskolin-induced cAMP accumulation by
l-glutamic acid. Copyright © 1996 Elsevier Science Ltd.</description><identifier>ISSN: 0028-3908</identifier><identifier>EISSN: 1873-7064</identifier><identifier>DOI: 10.1016/0028-3908(96)84622-3</identifier><identifier>PMID: 8887960</identifier><identifier>CODEN: NEPHBW</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>(1 S,3 R)-1-aminocyclopentane-1,3-dicarboxylic acid ; Amino Acid Sequence ; Aminoacid receptors (glycine, glutamate, gaba) ; Animals ; Baby Hamster ; Biological and medical sciences ; cAMP ; Cell receptors ; Cell structures and functions ; Cricetinae ; Cyclic AMP - metabolism ; Dose-Response Relationship, Drug ; Fundamental and applied biological sciences. Psychology ; Glutamate ; Glutamic Acid - pharmacology ; Human metabotropic glutamate receptor ; Humans ; Immunohistochemistry ; In Situ Hybridization ; Kidney ; Methylcarboxyphenylglycine ; Molecular and cellular biology ; Molecular Sequence Data ; Rats ; Receptors, Metabotropic Glutamate - genetics</subject><ispartof>Neuropharmacology, 1996-05, Vol.35 (5), p.523-530</ispartof><rights>1996 Elsevier Science Ltd</rights><rights>1996 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c417t-5a4c7c1240486e6b60032c678cb4f0c674872add5972cc17ede72b52a23b79783</citedby><cites>FETCH-LOGICAL-c417t-5a4c7c1240486e6b60032c678cb4f0c674872add5972cc17ede72b52a23b79783</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3225270$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8887960$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>EMILE, LYDIA</creatorcontrib><creatorcontrib>MERCKEN, LUC</creatorcontrib><creatorcontrib>APIOU, FRANCOISE</creatorcontrib><creatorcontrib>PRADIER, LAURENT</creatorcontrib><creatorcontrib>BOCK, MARIE-DOMINIQUE</creatorcontrib><creatorcontrib>MENAGER, JEAN</creatorcontrib><creatorcontrib>CLOT, JOSETTE</creatorcontrib><creatorcontrib>DOBLE, ADAM</creatorcontrib><creatorcontrib>BLANCHARD, JEAN-CHARLES</creatorcontrib><title>Molecular Cloning, Functional Expression, Pharmacological Characterization and Chromosomal Localization of the Human Metabotropic Glutamate Receptor Type 3</title><title>Neuropharmacology</title><addtitle>Neuropharmacology</addtitle><description>Glutamic acid is the major excitatory amino acid of the central nervous system which interacts with two receptor families, the ionotropic and metabotropic glutamate receptors. The metabotropic glutamate receptors (mGluRs) are coupled to G proteins and can be divided into three subgroups based on their sequence homology, signal transduction pathway and pharmacology. In this study, we describe the cloning of the cDNA encoding the human metabotropic glutamate receptor type 3 (HmGluR3). It was obtained by reverse transcription-polymerase chain reaction (RT-PCR) with degenerate oligonucleotides corresponding to highly conserved sequences between rat mGluRs. The receptor shows 879 amino acids with 96% amino acid sequence identity with rat mGluR3. It is strongly expressed in fetal and adult whole brain, especially in caudate nucleus and corpus callosum. The gene was identified by fluorescence
in situ hybridization on chromosome 7 band q22. Activation of the human mGluR3, permanently expressed in Baby Hamster Kidney (BHK) cells, by excitatory amino acid inhibits the forskolin-stimulated accumulation of intracellular cAMP. The rank order of potency is
l-glutamic acid ⩾ (1
S,3
R)-1-aminocyclopentane-1,3-dicarboxylic acid ((1
S,3
R)-ACPD) >> ibotenic acid > quisqualic acid. (
RS)-α-methyl-4-carboxyphenylglycine [(
RS)-MCPG, 1 mM] is without effect on inhibition of forskolin-induced cAMP accumulation by
l-glutamic acid. Copyright © 1996 Elsevier Science Ltd.</description><subject>(1 S,3 R)-1-aminocyclopentane-1,3-dicarboxylic acid</subject><subject>Amino Acid Sequence</subject><subject>Aminoacid receptors (glycine, glutamate, gaba)</subject><subject>Animals</subject><subject>Baby Hamster</subject><subject>Biological and medical sciences</subject><subject>cAMP</subject><subject>Cell receptors</subject><subject>Cell structures and functions</subject><subject>Cricetinae</subject><subject>Cyclic AMP - metabolism</subject><subject>Dose-Response Relationship, Drug</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glutamate</subject><subject>Glutamic Acid - pharmacology</subject><subject>Human metabotropic glutamate receptor</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>In Situ Hybridization</subject><subject>Kidney</subject><subject>Methylcarboxyphenylglycine</subject><subject>Molecular and cellular biology</subject><subject>Molecular Sequence Data</subject><subject>Rats</subject><subject>Receptors, Metabotropic Glutamate - genetics</subject><issn>0028-3908</issn><issn>1873-7064</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><recordid>eNqFkd1u1DAQhSMEKkvhDUDyBUJFasB2HNu5QUKr_iBtBULl2nImk9YoiVPbQS2vwsviZZe9hCt7fL4Z2-cUxUtG3zHK5HtKuS6rhuqTRr7VQnJeVo-KFdOqKhWV4nGxOiBPi2cxfqeUCs30UXGktVaNpKvi15UfEJbBBrIe_OSmm1NyvkyQnJ_sQM7u54Ax5uKUfLm1YbTgB3_jIGvrXFtIGNxPu8WJnbp8GPzoox8zsPEZ-yv6nqRbJJfLaCdyhcm2PgU_OyAXw5LsaBOSrwg4Jx_I9cOMpHpePOntEPHFfj0uvp2fXa8vy83ni0_rj5sSBFOprK0ABYyL_DmJspWUVhyk0tCKnuaN0IrbrqsbxQGYwg4Vb2tuedWqRunquHizmzsHf7dgTGZ0EXAY7IR-iUZpkf2U6r8gqzVXlLEMih0IwccYsDdzcKMND4ZRsw3PbJMx22RMI82f8EyV217t5y_tiN2haZ9W1l_vdRuztX2wE7h4wCrO63x_xj7sMMym_XAYTASHE2DnAkIynXf_fsdvLAG3xQ</recordid><startdate>19960501</startdate><enddate>19960501</enddate><creator>EMILE, LYDIA</creator><creator>MERCKEN, LUC</creator><creator>APIOU, FRANCOISE</creator><creator>PRADIER, LAURENT</creator><creator>BOCK, MARIE-DOMINIQUE</creator><creator>MENAGER, JEAN</creator><creator>CLOT, JOSETTE</creator><creator>DOBLE, ADAM</creator><creator>BLANCHARD, JEAN-CHARLES</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><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>7TK</scope><scope>7X8</scope></search><sort><creationdate>19960501</creationdate><title>Molecular Cloning, Functional Expression, Pharmacological Characterization and Chromosomal Localization of the Human Metabotropic Glutamate Receptor Type 3</title><author>EMILE, LYDIA ; MERCKEN, LUC ; APIOU, FRANCOISE ; PRADIER, LAURENT ; BOCK, MARIE-DOMINIQUE ; MENAGER, JEAN ; CLOT, JOSETTE ; DOBLE, ADAM ; BLANCHARD, JEAN-CHARLES</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-5a4c7c1240486e6b60032c678cb4f0c674872add5972cc17ede72b52a23b79783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>(1 S,3 R)-1-aminocyclopentane-1,3-dicarboxylic acid</topic><topic>Amino Acid Sequence</topic><topic>Aminoacid receptors (glycine, glutamate, gaba)</topic><topic>Animals</topic><topic>Baby Hamster</topic><topic>Biological and medical sciences</topic><topic>cAMP</topic><topic>Cell receptors</topic><topic>Cell structures and functions</topic><topic>Cricetinae</topic><topic>Cyclic AMP - metabolism</topic><topic>Dose-Response Relationship, Drug</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glutamate</topic><topic>Glutamic Acid - pharmacology</topic><topic>Human metabotropic glutamate receptor</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>In Situ Hybridization</topic><topic>Kidney</topic><topic>Methylcarboxyphenylglycine</topic><topic>Molecular and cellular biology</topic><topic>Molecular Sequence Data</topic><topic>Rats</topic><topic>Receptors, Metabotropic Glutamate - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>EMILE, LYDIA</creatorcontrib><creatorcontrib>MERCKEN, LUC</creatorcontrib><creatorcontrib>APIOU, FRANCOISE</creatorcontrib><creatorcontrib>PRADIER, LAURENT</creatorcontrib><creatorcontrib>BOCK, MARIE-DOMINIQUE</creatorcontrib><creatorcontrib>MENAGER, JEAN</creatorcontrib><creatorcontrib>CLOT, JOSETTE</creatorcontrib><creatorcontrib>DOBLE, ADAM</creatorcontrib><creatorcontrib>BLANCHARD, JEAN-CHARLES</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Neuropharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>EMILE, LYDIA</au><au>MERCKEN, LUC</au><au>APIOU, FRANCOISE</au><au>PRADIER, LAURENT</au><au>BOCK, MARIE-DOMINIQUE</au><au>MENAGER, JEAN</au><au>CLOT, JOSETTE</au><au>DOBLE, ADAM</au><au>BLANCHARD, JEAN-CHARLES</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular Cloning, Functional Expression, Pharmacological Characterization and Chromosomal Localization of the Human Metabotropic Glutamate Receptor Type 3</atitle><jtitle>Neuropharmacology</jtitle><addtitle>Neuropharmacology</addtitle><date>1996-05-01</date><risdate>1996</risdate><volume>35</volume><issue>5</issue><spage>523</spage><epage>530</epage><pages>523-530</pages><issn>0028-3908</issn><eissn>1873-7064</eissn><coden>NEPHBW</coden><abstract>Glutamic acid is the major excitatory amino acid of the central nervous system which interacts with two receptor families, the ionotropic and metabotropic glutamate receptors. The metabotropic glutamate receptors (mGluRs) are coupled to G proteins and can be divided into three subgroups based on their sequence homology, signal transduction pathway and pharmacology. In this study, we describe the cloning of the cDNA encoding the human metabotropic glutamate receptor type 3 (HmGluR3). It was obtained by reverse transcription-polymerase chain reaction (RT-PCR) with degenerate oligonucleotides corresponding to highly conserved sequences between rat mGluRs. The receptor shows 879 amino acids with 96% amino acid sequence identity with rat mGluR3. It is strongly expressed in fetal and adult whole brain, especially in caudate nucleus and corpus callosum. The gene was identified by fluorescence
in situ hybridization on chromosome 7 band q22. Activation of the human mGluR3, permanently expressed in Baby Hamster Kidney (BHK) cells, by excitatory amino acid inhibits the forskolin-stimulated accumulation of intracellular cAMP. The rank order of potency is
l-glutamic acid ⩾ (1
S,3
R)-1-aminocyclopentane-1,3-dicarboxylic acid ((1
S,3
R)-ACPD) >> ibotenic acid > quisqualic acid. (
RS)-α-methyl-4-carboxyphenylglycine [(
RS)-MCPG, 1 mM] is without effect on inhibition of forskolin-induced cAMP accumulation by
l-glutamic acid. Copyright © 1996 Elsevier Science Ltd.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>8887960</pmid><doi>10.1016/0028-3908(96)84622-3</doi><tpages>8</tpages></addata></record> |
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ispartof | Neuropharmacology, 1996-05, Vol.35 (5), p.523-530 |
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language | eng |
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source | ScienceDirect Journals |
subjects | (1 S,3 R)-1-aminocyclopentane-1,3-dicarboxylic acid Amino Acid Sequence Aminoacid receptors (glycine, glutamate, gaba) Animals Baby Hamster Biological and medical sciences cAMP Cell receptors Cell structures and functions Cricetinae Cyclic AMP - metabolism Dose-Response Relationship, Drug Fundamental and applied biological sciences. Psychology Glutamate Glutamic Acid - pharmacology Human metabotropic glutamate receptor Humans Immunohistochemistry In Situ Hybridization Kidney Methylcarboxyphenylglycine Molecular and cellular biology Molecular Sequence Data Rats Receptors, Metabotropic Glutamate - genetics |
title | Molecular Cloning, Functional Expression, Pharmacological Characterization and Chromosomal Localization of the Human Metabotropic Glutamate Receptor Type 3 |
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