Murine MHC class Ib gene, H2-M2, encodes a conserved surface-expressed glycoprotein
We have determined the genomic sequence of H2-M2 in seven haplotypes from nine inbred strains of mice and in five wild-derived haplotypes. Except for the spretus haplotype sp1 with a premature stop codon, we found only limited polymorphism. Four of the five amino acid substitutions in the alpha-heli...
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description | We have determined the genomic sequence of H2-M2 in seven haplotypes from nine inbred strains of mice and in five wild-derived haplotypes. Except for the spretus haplotype sp1 with a premature stop codon, we found only limited polymorphism. Four of the five amino acid substitutions in the alpha-helices are at positions that would point out from the antigen-binding groove, indicating that the polymorphism might influence receptor recognition rather than antigen binding. The rat homologue, RT1.M2(lv1), has 89% identity to H2-M2 at the nucleotide level and 91% at the amino acid level, and it also encodes an intact MHC class I glycoprotein. Chimeric proteins with alpha(1)alpha(2) or alpha(3)-transmembrane domains encoded by H2-Q9 were detectable on the surface of transfectants with monoclonal antibodies against Qa2, and the full-length M2 protein, labeled by fusion with green fluorescent protein, was detectable with S19.8 monoclonal antibodies. The H2-M2 protein was thus expressed on the cell surface, even in TAP-deficient RMA-S cells at 37 degrees C, suggesting that it is TAP-independent. We conclude that H2-M2 is a conserved mouse class Ib gene that is translated to a surface-expressed MHC class I molecule with a function still to be elucidated. |
doi_str_mv | 10.1007/s00251-004-0661-6 |
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Except for the spretus haplotype sp1 with a premature stop codon, we found only limited polymorphism. Four of the five amino acid substitutions in the alpha-helices are at positions that would point out from the antigen-binding groove, indicating that the polymorphism might influence receptor recognition rather than antigen binding. The rat homologue, RT1.M2(lv1), has 89% identity to H2-M2 at the nucleotide level and 91% at the amino acid level, and it also encodes an intact MHC class I glycoprotein. Chimeric proteins with alpha(1)alpha(2) or alpha(3)-transmembrane domains encoded by H2-Q9 were detectable on the surface of transfectants with monoclonal antibodies against Qa2, and the full-length M2 protein, labeled by fusion with green fluorescent protein, was detectable with S19.8 monoclonal antibodies. The H2-M2 protein was thus expressed on the cell surface, even in TAP-deficient RMA-S cells at 37 degrees C, suggesting that it is TAP-independent. We conclude that H2-M2 is a conserved mouse class Ib gene that is translated to a surface-expressed MHC class I molecule with a function still to be elucidated.</description><identifier>ISSN: 0093-7711</identifier><identifier>EISSN: 1432-1211</identifier><identifier>DOI: 10.1007/s00251-004-0661-6</identifier><identifier>PMID: 15045471</identifier><language>eng</language><publisher>United States: Springer Nature B.V</publisher><subject>Alternative Splicing ; Amino Acid Sequence ; Amino acids ; Animals ; Base Sequence ; Cloning, Molecular ; Conserved Sequence ; DNA, Complementary - genetics ; Genes, MHC Class I ; Haplotypes ; HeLa Cells ; Histocompatibility Antigens - genetics ; Histocompatibility Antigens Class II - genetics ; Humans ; Membrane Glycoproteins - genetics ; Membrane Glycoproteins - immunology ; Mice ; Mice, Inbred Strains ; Molecular Sequence Data ; Phylogeny ; Polymorphism, Genetic ; Proteins ; Rats ; Recombinant Fusion Proteins - genetics ; Recombinant Fusion Proteins - immunology ; Sequence Homology, Amino Acid ; Transfection</subject><ispartof>Immunogenetics (New York), 2004-04, Vol.56 (1), p.1-11</ispartof><rights>Springer-Verlag 2004</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c355t-40f12e439b2f86bcdeaa1f2c602ebf92567a55133192f71ab3e755ec9a883a303</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15045471$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Moore, Yuki F</creatorcontrib><creatorcontrib>Lambracht-Washington, Doris</creatorcontrib><creatorcontrib>Tabaczewski, Piotr</creatorcontrib><creatorcontrib>Fischer Lindahl, Kirsten</creatorcontrib><title>Murine MHC class Ib gene, H2-M2, encodes a conserved surface-expressed glycoprotein</title><title>Immunogenetics (New York)</title><addtitle>Immunogenetics</addtitle><description>We have determined the genomic sequence of H2-M2 in seven haplotypes from nine inbred strains of mice and in five wild-derived haplotypes. Except for the spretus haplotype sp1 with a premature stop codon, we found only limited polymorphism. Four of the five amino acid substitutions in the alpha-helices are at positions that would point out from the antigen-binding groove, indicating that the polymorphism might influence receptor recognition rather than antigen binding. The rat homologue, RT1.M2(lv1), has 89% identity to H2-M2 at the nucleotide level and 91% at the amino acid level, and it also encodes an intact MHC class I glycoprotein. Chimeric proteins with alpha(1)alpha(2) or alpha(3)-transmembrane domains encoded by H2-Q9 were detectable on the surface of transfectants with monoclonal antibodies against Qa2, and the full-length M2 protein, labeled by fusion with green fluorescent protein, was detectable with S19.8 monoclonal antibodies. The H2-M2 protein was thus expressed on the cell surface, even in TAP-deficient RMA-S cells at 37 degrees C, suggesting that it is TAP-independent. We conclude that H2-M2 is a conserved mouse class Ib gene that is translated to a surface-expressed MHC class I molecule with a function still to be elucidated.</description><subject>Alternative Splicing</subject><subject>Amino Acid Sequence</subject><subject>Amino acids</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Cloning, Molecular</subject><subject>Conserved Sequence</subject><subject>DNA, Complementary - genetics</subject><subject>Genes, MHC Class I</subject><subject>Haplotypes</subject><subject>HeLa Cells</subject><subject>Histocompatibility Antigens - genetics</subject><subject>Histocompatibility Antigens Class II - genetics</subject><subject>Humans</subject><subject>Membrane Glycoproteins - genetics</subject><subject>Membrane Glycoproteins - immunology</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Molecular Sequence Data</subject><subject>Phylogeny</subject><subject>Polymorphism, Genetic</subject><subject>Proteins</subject><subject>Rats</subject><subject>Recombinant Fusion Proteins - genetics</subject><subject>Recombinant Fusion Proteins - immunology</subject><subject>Sequence Homology, Amino Acid</subject><subject>Transfection</subject><issn>0093-7711</issn><issn>1432-1211</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkcFKAzEQhoMoWqsP4EWCB09GZ5JN0hylqBUsHtRzyKazpbLdrUlX9O3d0oLgxdPA8M0_M3yMnSFcI4C9yQBSowAoBBiDwuyxARZKCpSI-2wA4JSwFvGIHef8DoDaSXPIjlBDoQuLA_Yy7dKiIT6djHmsQ878seRzauiKT6SYyitOTWxnlHngsW0ypU-a8dylKkQS9LVKlHPfmdffsV2ldk2L5oQdVKHOdLqrQ_Z2f_c6noin54fH8e2TiErrtSigQkmFcqWsRqaMMwoBKxkNSCorJ7WxQWtUCp2sLIZSkdWaogujkQoK1JBdbnP7vR8d5bVfLnKkug4NtV32FkeFNPA_iNYp67TpwYs_4HvbpaZ_whvZHy2t26ThFoqpzTlR5VdpsQzp2yP4jRe_9eJ7L37jxW-Cz3fBXbmk2e_EToT6AXe4hd0</recordid><startdate>200404</startdate><enddate>200404</enddate><creator>Moore, Yuki F</creator><creator>Lambracht-Washington, Doris</creator><creator>Tabaczewski, Piotr</creator><creator>Fischer Lindahl, Kirsten</creator><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>7QL</scope><scope>7T5</scope><scope>7T7</scope><scope>7TK</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</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>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>200404</creationdate><title>Murine MHC class Ib gene, H2-M2, encodes a conserved surface-expressed glycoprotein</title><author>Moore, Yuki F ; Lambracht-Washington, Doris ; Tabaczewski, Piotr ; Fischer Lindahl, Kirsten</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c355t-40f12e439b2f86bcdeaa1f2c602ebf92567a55133192f71ab3e755ec9a883a303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Alternative Splicing</topic><topic>Amino Acid Sequence</topic><topic>Amino acids</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Cloning, Molecular</topic><topic>Conserved Sequence</topic><topic>DNA, Complementary - genetics</topic><topic>Genes, MHC Class I</topic><topic>Haplotypes</topic><topic>HeLa Cells</topic><topic>Histocompatibility Antigens - genetics</topic><topic>Histocompatibility Antigens Class II - genetics</topic><topic>Humans</topic><topic>Membrane Glycoproteins - genetics</topic><topic>Membrane Glycoproteins - immunology</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Molecular Sequence Data</topic><topic>Phylogeny</topic><topic>Polymorphism, Genetic</topic><topic>Proteins</topic><topic>Rats</topic><topic>Recombinant Fusion Proteins - genetics</topic><topic>Recombinant Fusion Proteins - immunology</topic><topic>Sequence Homology, Amino Acid</topic><topic>Transfection</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Moore, Yuki F</creatorcontrib><creatorcontrib>Lambracht-Washington, Doris</creatorcontrib><creatorcontrib>Tabaczewski, Piotr</creatorcontrib><creatorcontrib>Fischer Lindahl, Kirsten</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>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>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>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 Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</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>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</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>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Immunogenetics (New York)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moore, Yuki F</au><au>Lambracht-Washington, Doris</au><au>Tabaczewski, Piotr</au><au>Fischer Lindahl, Kirsten</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Murine MHC class Ib gene, H2-M2, encodes a conserved surface-expressed glycoprotein</atitle><jtitle>Immunogenetics (New York)</jtitle><addtitle>Immunogenetics</addtitle><date>2004-04</date><risdate>2004</risdate><volume>56</volume><issue>1</issue><spage>1</spage><epage>11</epage><pages>1-11</pages><issn>0093-7711</issn><eissn>1432-1211</eissn><abstract>We have determined the genomic sequence of H2-M2 in seven haplotypes from nine inbred strains of mice and in five wild-derived haplotypes. Except for the spretus haplotype sp1 with a premature stop codon, we found only limited polymorphism. Four of the five amino acid substitutions in the alpha-helices are at positions that would point out from the antigen-binding groove, indicating that the polymorphism might influence receptor recognition rather than antigen binding. The rat homologue, RT1.M2(lv1), has 89% identity to H2-M2 at the nucleotide level and 91% at the amino acid level, and it also encodes an intact MHC class I glycoprotein. Chimeric proteins with alpha(1)alpha(2) or alpha(3)-transmembrane domains encoded by H2-Q9 were detectable on the surface of transfectants with monoclonal antibodies against Qa2, and the full-length M2 protein, labeled by fusion with green fluorescent protein, was detectable with S19.8 monoclonal antibodies. The H2-M2 protein was thus expressed on the cell surface, even in TAP-deficient RMA-S cells at 37 degrees C, suggesting that it is TAP-independent. We conclude that H2-M2 is a conserved mouse class Ib gene that is translated to a surface-expressed MHC class I molecule with a function still to be elucidated.</abstract><cop>United States</cop><pub>Springer Nature B.V</pub><pmid>15045471</pmid><doi>10.1007/s00251-004-0661-6</doi><tpages>11</tpages></addata></record> |
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subjects | Alternative Splicing Amino Acid Sequence Amino acids Animals Base Sequence Cloning, Molecular Conserved Sequence DNA, Complementary - genetics Genes, MHC Class I Haplotypes HeLa Cells Histocompatibility Antigens - genetics Histocompatibility Antigens Class II - genetics Humans Membrane Glycoproteins - genetics Membrane Glycoproteins - immunology Mice Mice, Inbred Strains Molecular Sequence Data Phylogeny Polymorphism, Genetic Proteins Rats Recombinant Fusion Proteins - genetics Recombinant Fusion Proteins - immunology Sequence Homology, Amino Acid Transfection |
title | Murine MHC class Ib gene, H2-M2, encodes a conserved surface-expressed glycoprotein |
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