Melanin-Concentrating Hormone Receptor Subtypes 1 and 2: Species-Specific Gene Expression
To assess the contribution of potential central nervous system pathways implicated in the control of appetite regulation and energy metabolism, it is essential to first identify appropriate animal models. Melanin-concentrating hormone (MCH), a conserved cyclic neuropeptide implicated in the modulati...
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Veröffentlicht in: | Genomics (San Diego, Calif.) Calif.), 2002-06, Vol.79 (6), p.785-792 |
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creator | Tan, Carina P. Sano, Hideki Iwaasa, Hisashi Pan, Jie Sailer, Andreas W. Hreniuk, Donna L. Feighner, Scott D. Palyha, Oksana C. Pong, Sheng-Shung Figueroa, David J. Austin, Christopher P. Jiang, Michael M. Yu, Hong Ito, Junko Ito, Makoto Ito, Masahiko Guan, Xiao Ming MacNeil, Douglas J. Kanatani, Akio Van der Ploeg, Lex H.T. Howard, Andrew D. |
description | To assess the contribution of potential central nervous system pathways implicated in the control of appetite regulation and energy metabolism, it is essential to first identify appropriate animal models. Melanin-concentrating hormone (MCH), a conserved cyclic neuropeptide implicated in the modulation of food intake, has been shown to bind and activate two G-protein-coupled receptors, called GPR24 and MCHR2, expressed in human brain and other tissues. Here we show that several non-human species (rat, mouse, hamster, guinea pig, and rabbit) do not have functional MCHR2 receptors, or encode a nonfunctional MCHR2 pseudogene while retaining GPR24 expression. We identified three species for further evaluation that express both MCH receptor subtypes. We cloned and functionally characterized dog, ferret, and rhesus GPR24 and MCHR2 in mammalian cells and studied their brain distribution patterns by in situ hybridization. The homology, expression profile, and functional similarity of the receptors in the dog, ferret, and rhesus to that of human support the potential use of these species as preclinical animal models in the development of therapeutic agents for obesity or other MCH-mediated disorders. |
doi_str_mv | 10.1006/geno.2002.6771 |
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Melanin-concentrating hormone (MCH), a conserved cyclic neuropeptide implicated in the modulation of food intake, has been shown to bind and activate two G-protein-coupled receptors, called GPR24 and MCHR2, expressed in human brain and other tissues. Here we show that several non-human species (rat, mouse, hamster, guinea pig, and rabbit) do not have functional MCHR2 receptors, or encode a nonfunctional MCHR2 pseudogene while retaining GPR24 expression. We identified three species for further evaluation that express both MCH receptor subtypes. We cloned and functionally characterized dog, ferret, and rhesus GPR24 and MCHR2 in mammalian cells and studied their brain distribution patterns by in situ hybridization. The homology, expression profile, and functional similarity of the receptors in the dog, ferret, and rhesus to that of human support the potential use of these species as preclinical animal models in the development of therapeutic agents for obesity or other MCH-mediated disorders.</description><identifier>ISSN: 0888-7543</identifier><identifier>EISSN: 1089-8646</identifier><identifier>DOI: 10.1006/geno.2002.6771</identifier><identifier>PMID: 12036292</identifier><language>eng</language><publisher>San Diego, CA: Elsevier Inc</publisher><subject>Amino Acid Sequence ; Animals ; Biological and medical sciences ; Fundamental and applied biological sciences. Psychology ; Gene Expression Regulation ; Genes. 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Melanin-concentrating hormone (MCH), a conserved cyclic neuropeptide implicated in the modulation of food intake, has been shown to bind and activate two G-protein-coupled receptors, called GPR24 and MCHR2, expressed in human brain and other tissues. Here we show that several non-human species (rat, mouse, hamster, guinea pig, and rabbit) do not have functional MCHR2 receptors, or encode a nonfunctional MCHR2 pseudogene while retaining GPR24 expression. We identified three species for further evaluation that express both MCH receptor subtypes. We cloned and functionally characterized dog, ferret, and rhesus GPR24 and MCHR2 in mammalian cells and studied their brain distribution patterns by in situ hybridization. The homology, expression profile, and functional similarity of the receptors in the dog, ferret, and rhesus to that of human support the potential use of these species as preclinical animal models in the development of therapeutic agents for obesity or other MCH-mediated disorders.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression Regulation</subject><subject>Genes. Genome</subject><subject>Humans</subject><subject>Mammals - genetics</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Molecular Sequence Data</subject><subject>Organ Specificity</subject><subject>Receptors, G-Protein-Coupled</subject><subject>Receptors, Pituitary Hormone - genetics</subject><subject>Receptors, Somatostatin - genetics</subject><subject>Sequence Alignment</subject><subject>Species Specificity</subject><issn>0888-7543</issn><issn>1089-8646</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkTtPKzEQRi10EYRHS4m2ubfbMPY6tpcORbwkEBKPgspyvGNklNiLvUGXf49DIlEhqmnON5rvDCFHFMYUQJy8YIhjBsDGQkq6RUYUVFsrwcUfMgKlVC0nvNklezm_AkDbKLZDdimDRrCWjcjzLc5N8KGexmAxDMkMPrxUVzEtYsDqHi32Q0zVw3I2fPSYK1qZ0FXstHro0XrM9dd03laXWALn__uEOfsYDsi2M_OMh5u5T54uzh-nV_XN3eX19OymtlzIobZUMoegDJMNCsodZ7O2Qc47aJlSHQJOmEEqJlY52yps0eGscdYKaZCLZp_8W-_tU3xbYh70wmeL81IL4zJrSaVkDH4HqeKUM0ELOF6DNsWcEzrdJ78w6UNT0CvremVdr6zrlfUSON5sXs4W2H3jG80F-LsBTLZm7pIJ1udvrpFAS_fCqTWHRdi7x6RzcVwe0_mEdtBd9D_d8AnS-Z3M</recordid><startdate>20020601</startdate><enddate>20020601</enddate><creator>Tan, Carina P.</creator><creator>Sano, Hideki</creator><creator>Iwaasa, Hisashi</creator><creator>Pan, Jie</creator><creator>Sailer, Andreas W.</creator><creator>Hreniuk, Donna L.</creator><creator>Feighner, Scott D.</creator><creator>Palyha, Oksana C.</creator><creator>Pong, Sheng-Shung</creator><creator>Figueroa, David J.</creator><creator>Austin, Christopher P.</creator><creator>Jiang, Michael M.</creator><creator>Yu, Hong</creator><creator>Ito, Junko</creator><creator>Ito, Makoto</creator><creator>Ito, Masahiko</creator><creator>Guan, Xiao Ming</creator><creator>MacNeil, Douglas J.</creator><creator>Kanatani, Akio</creator><creator>Van der Ploeg, Lex H.T.</creator><creator>Howard, Andrew D.</creator><general>Elsevier Inc</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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20020601</creationdate><title>Melanin-Concentrating Hormone Receptor Subtypes 1 and 2: Species-Specific Gene Expression</title><author>Tan, Carina P. ; Sano, Hideki ; Iwaasa, Hisashi ; Pan, Jie ; Sailer, Andreas W. ; Hreniuk, Donna L. ; Feighner, Scott D. ; Palyha, Oksana C. ; Pong, Sheng-Shung ; Figueroa, David J. ; Austin, Christopher P. ; Jiang, Michael M. ; Yu, Hong ; Ito, Junko ; Ito, Makoto ; Ito, Masahiko ; Guan, Xiao Ming ; MacNeil, Douglas J. ; Kanatani, Akio ; Van der Ploeg, Lex H.T. ; Howard, Andrew D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c467t-c172fe08a273e614f42b93e44d09288de0e52ae165c8fc98e9efeb3fcc67ae463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression Regulation</topic><topic>Genes. Genome</topic><topic>Humans</topic><topic>Mammals - genetics</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>Molecular Sequence Data</topic><topic>Organ Specificity</topic><topic>Receptors, G-Protein-Coupled</topic><topic>Receptors, Pituitary Hormone - genetics</topic><topic>Receptors, Somatostatin - genetics</topic><topic>Sequence Alignment</topic><topic>Species Specificity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tan, Carina P.</creatorcontrib><creatorcontrib>Sano, Hideki</creatorcontrib><creatorcontrib>Iwaasa, Hisashi</creatorcontrib><creatorcontrib>Pan, Jie</creatorcontrib><creatorcontrib>Sailer, Andreas W.</creatorcontrib><creatorcontrib>Hreniuk, Donna L.</creatorcontrib><creatorcontrib>Feighner, Scott D.</creatorcontrib><creatorcontrib>Palyha, Oksana C.</creatorcontrib><creatorcontrib>Pong, Sheng-Shung</creatorcontrib><creatorcontrib>Figueroa, David J.</creatorcontrib><creatorcontrib>Austin, Christopher P.</creatorcontrib><creatorcontrib>Jiang, Michael M.</creatorcontrib><creatorcontrib>Yu, Hong</creatorcontrib><creatorcontrib>Ito, Junko</creatorcontrib><creatorcontrib>Ito, Makoto</creatorcontrib><creatorcontrib>Ito, Masahiko</creatorcontrib><creatorcontrib>Guan, Xiao Ming</creatorcontrib><creatorcontrib>MacNeil, Douglas J.</creatorcontrib><creatorcontrib>Kanatani, Akio</creatorcontrib><creatorcontrib>Van der Ploeg, Lex H.T.</creatorcontrib><creatorcontrib>Howard, Andrew D.</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>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Genomics (San Diego, Calif.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tan, Carina P.</au><au>Sano, Hideki</au><au>Iwaasa, Hisashi</au><au>Pan, Jie</au><au>Sailer, Andreas W.</au><au>Hreniuk, Donna L.</au><au>Feighner, Scott D.</au><au>Palyha, Oksana C.</au><au>Pong, Sheng-Shung</au><au>Figueroa, David J.</au><au>Austin, Christopher P.</au><au>Jiang, Michael M.</au><au>Yu, Hong</au><au>Ito, Junko</au><au>Ito, Makoto</au><au>Ito, Masahiko</au><au>Guan, Xiao Ming</au><au>MacNeil, Douglas J.</au><au>Kanatani, Akio</au><au>Van der Ploeg, Lex H.T.</au><au>Howard, Andrew D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Melanin-Concentrating Hormone Receptor Subtypes 1 and 2: Species-Specific Gene Expression</atitle><jtitle>Genomics (San Diego, Calif.)</jtitle><addtitle>Genomics</addtitle><date>2002-06-01</date><risdate>2002</risdate><volume>79</volume><issue>6</issue><spage>785</spage><epage>792</epage><pages>785-792</pages><issn>0888-7543</issn><eissn>1089-8646</eissn><abstract>To assess the contribution of potential central nervous system pathways implicated in the control of appetite regulation and energy metabolism, it is essential to first identify appropriate animal models. Melanin-concentrating hormone (MCH), a conserved cyclic neuropeptide implicated in the modulation of food intake, has been shown to bind and activate two G-protein-coupled receptors, called GPR24 and MCHR2, expressed in human brain and other tissues. Here we show that several non-human species (rat, mouse, hamster, guinea pig, and rabbit) do not have functional MCHR2 receptors, or encode a nonfunctional MCHR2 pseudogene while retaining GPR24 expression. We identified three species for further evaluation that express both MCH receptor subtypes. We cloned and functionally characterized dog, ferret, and rhesus GPR24 and MCHR2 in mammalian cells and studied their brain distribution patterns by in situ hybridization. The homology, expression profile, and functional similarity of the receptors in the dog, ferret, and rhesus to that of human support the potential use of these species as preclinical animal models in the development of therapeutic agents for obesity or other MCH-mediated disorders.</abstract><cop>San Diego, CA</cop><pub>Elsevier Inc</pub><pmid>12036292</pmid><doi>10.1006/geno.2002.6771</doi><tpages>8</tpages></addata></record> |
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subjects | Amino Acid Sequence Animals Biological and medical sciences Fundamental and applied biological sciences. Psychology Gene Expression Regulation Genes. Genome Humans Mammals - genetics Molecular and cellular biology Molecular genetics Molecular Sequence Data Organ Specificity Receptors, G-Protein-Coupled Receptors, Pituitary Hormone - genetics Receptors, Somatostatin - genetics Sequence Alignment Species Specificity |
title | Melanin-Concentrating Hormone Receptor Subtypes 1 and 2: Species-Specific Gene Expression |
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