Analysis of the genomic region containing the tammar wallaby (Macropus eugenii) orthologues of MHC class III genes
Major histocompatibility complex (MHC) molecules are central to development and regulation of the immune system in all jawed vertebrates. MHC class III cytokine genes from the tumor necrosis factor core family, including tumor necrosis factor (TNF) and lymphotoxin alpha and beta (LTA, LTB), are well...
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creator | Cross, J.G.R. Harrison, G.A. Coggill, P. Sims, S. Beck, S. Deakin, J.E. Marshall Graves, J.A. |
description | Major histocompatibility complex (MHC) molecules are central to development and regulation of the immune system in all jawed vertebrates. MHC class III cytokine genes from the tumor necrosis factor core family, including tumor necrosis factor (TNF) and lymphotoxin alpha and beta (LTA, LTB), are well studied in human and mouse. Orthologues have been identified in several other eutherian species and the cDNA sequences have been reported for a model marsupial, the tammar wallaby. Comparative genomics can help to determine gene function, to understand the evolution of a gene or gene family, and to identify potential regulatory regions. We therefore cloned the genomic region containing the tammar LTB, TNF, and LTA orthologues by “genome walking”, using primers designed from known tammar sequences and regions conserved in other species. We isolated two tammar BAC clones containing all three genes. These tammar genes show similar intergenic distances and the same transcriptional orientation as in human and mouse. Gene structures and sequences are also very conserved. By comparing the tammar, human and mouse genomic sequences we were able to identify candidate regulatory regions for these genes in mammals. Full length sequencing of BACs containing the three genes has been partially completed, and reveals the presence of a number of other tammar MHC III orthologues in this region. |
doi_str_mv | 10.1159/000086379 |
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MHC class III cytokine genes from the tumor necrosis factor core family, including tumor necrosis factor (TNF) and lymphotoxin alpha and beta (LTA, LTB), are well studied in human and mouse. Orthologues have been identified in several other eutherian species and the cDNA sequences have been reported for a model marsupial, the tammar wallaby. Comparative genomics can help to determine gene function, to understand the evolution of a gene or gene family, and to identify potential regulatory regions. We therefore cloned the genomic region containing the tammar LTB, TNF, and LTA orthologues by “genome walking”, using primers designed from known tammar sequences and regions conserved in other species. We isolated two tammar BAC clones containing all three genes. These tammar genes show similar intergenic distances and the same transcriptional orientation as in human and mouse. Gene structures and sequences are also very conserved. By comparing the tammar, human and mouse genomic sequences we were able to identify candidate regulatory regions for these genes in mammals. Full length sequencing of BACs containing the three genes has been partially completed, and reveals the presence of a number of other tammar MHC III orthologues in this region. </description><identifier>ISSN: 1424-8581</identifier><identifier>EISSN: 1424-859X</identifier><identifier>DOI: 10.1159/000086379</identifier><identifier>PMID: 16103651</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Animals ; Base Sequence ; Chromosome Mapping ; Chromosomes, Artificial, Bacterial ; Chromosomes, Mammalian ; Cloning, Molecular ; Conserved Sequence ; DNA Primers ; Genome ; Humans ; Macropodidae - genetics ; Macropodidae - immunology ; Macropus eugenii ; Major Histocompatibility Complex ; Mice ; Molecular Sequence Data ; Original Article ; Polymerase Chain Reaction - methods ; Sequence Alignment ; Sequence Homology, Nucleic Acid ; Transcription, Genetic ; Tumor Necrosis Factor-alpha - genetics</subject><ispartof>Cytogenetic and genome research, 2005-01, Vol.111 (2), p.110-117</ispartof><rights>2005 S. Karger AG, Basel</rights><rights>Copyright (c) 2005 S. Karger AG, Basel</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c388t-873af1dff46344d843b60fa28f26bde24cef14b0cb56299f7138cb01c693c4cd3</citedby><cites>FETCH-LOGICAL-c388t-873af1dff46344d843b60fa28f26bde24cef14b0cb56299f7138cb01c693c4cd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,2424,27906,27907</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16103651$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cross, J.G.R.</creatorcontrib><creatorcontrib>Harrison, G.A.</creatorcontrib><creatorcontrib>Coggill, P.</creatorcontrib><creatorcontrib>Sims, S.</creatorcontrib><creatorcontrib>Beck, S.</creatorcontrib><creatorcontrib>Deakin, J.E.</creatorcontrib><creatorcontrib>Marshall Graves, J.A.</creatorcontrib><title>Analysis of the genomic region containing the tammar wallaby (Macropus eugenii) orthologues of MHC class III genes</title><title>Cytogenetic and genome research</title><addtitle>Cytogenet Genome Res</addtitle><description>Major histocompatibility complex (MHC) molecules are central to development and regulation of the immune system in all jawed vertebrates. MHC class III cytokine genes from the tumor necrosis factor core family, including tumor necrosis factor (TNF) and lymphotoxin alpha and beta (LTA, LTB), are well studied in human and mouse. Orthologues have been identified in several other eutherian species and the cDNA sequences have been reported for a model marsupial, the tammar wallaby. Comparative genomics can help to determine gene function, to understand the evolution of a gene or gene family, and to identify potential regulatory regions. We therefore cloned the genomic region containing the tammar LTB, TNF, and LTA orthologues by “genome walking”, using primers designed from known tammar sequences and regions conserved in other species. We isolated two tammar BAC clones containing all three genes. These tammar genes show similar intergenic distances and the same transcriptional orientation as in human and mouse. Gene structures and sequences are also very conserved. By comparing the tammar, human and mouse genomic sequences we were able to identify candidate regulatory regions for these genes in mammals. Full length sequencing of BACs containing the three genes has been partially completed, and reveals the presence of a number of other tammar MHC III orthologues in this region. </description><subject>Animals</subject><subject>Base Sequence</subject><subject>Chromosome Mapping</subject><subject>Chromosomes, Artificial, Bacterial</subject><subject>Chromosomes, Mammalian</subject><subject>Cloning, Molecular</subject><subject>Conserved Sequence</subject><subject>DNA Primers</subject><subject>Genome</subject><subject>Humans</subject><subject>Macropodidae - genetics</subject><subject>Macropodidae - immunology</subject><subject>Macropus eugenii</subject><subject>Major Histocompatibility Complex</subject><subject>Mice</subject><subject>Molecular Sequence Data</subject><subject>Original Article</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Sequence Alignment</subject><subject>Sequence Homology, Nucleic Acid</subject><subject>Transcription, Genetic</subject><subject>Tumor Necrosis Factor-alpha - genetics</subject><issn>1424-8581</issn><issn>1424-859X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqFkUtLAzEUhYMotj4WrgUJLkQX1bwmzSyl-ChYBFFwN2QyyTR1ZlKTGaT_3tiWFkQwmxu43z33cg4AJxhdY5ykNyg-wekw3QF9zAgbiCR93938Be6BgxBmCGHBEr4PephjRHmC-8DfNrJaBBugM7CdaljqxtVWQa9L6xqoXNNK29imXHZbWdfSwy9ZVTJfwMuJVN7NuwB1FwetvYLOt1NXubLTS8nJ4wiqSoYAx-Pxj7gOR2DPyCro43U9BG_3d6-jx8HT88N4dPs0UFSIdiCGVBpcGMM4ZawQjOYcGUmEITwvNGFKG8xypPKEkzQ1Q0yFyhFWPKWKqYIegouV7ty7z3hOm9U2KB0vb7TrQsYFEzhB5F-QIIFoQlEEz3-BM9f5aGBkCCMYDdM0QlcrKDoTgtcmm3sbTVtkGGU_cWWbuCJ7thbs8loXW3Kdz3bjh_Sl9htg9PCyVMjmhYnQ6Z_Qasc3t02jjw</recordid><startdate>20050101</startdate><enddate>20050101</enddate><creator>Cross, J.G.R.</creator><creator>Harrison, G.A.</creator><creator>Coggill, P.</creator><creator>Sims, S.</creator><creator>Beck, S.</creator><creator>Deakin, J.E.</creator><creator>Marshall Graves, J.A.</creator><general>S. 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genetics</topic><topic>Macropodidae - immunology</topic><topic>Macropus eugenii</topic><topic>Major Histocompatibility Complex</topic><topic>Mice</topic><topic>Molecular Sequence Data</topic><topic>Original Article</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Sequence Alignment</topic><topic>Sequence Homology, Nucleic Acid</topic><topic>Transcription, Genetic</topic><topic>Tumor Necrosis Factor-alpha - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cross, J.G.R.</creatorcontrib><creatorcontrib>Harrison, G.A.</creatorcontrib><creatorcontrib>Coggill, P.</creatorcontrib><creatorcontrib>Sims, S.</creatorcontrib><creatorcontrib>Beck, S.</creatorcontrib><creatorcontrib>Deakin, J.E.</creatorcontrib><creatorcontrib>Marshall Graves, J.A.</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>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences 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>Science Database (Alumni Edition)</collection><collection>STEM Database</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 Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</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>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>Science Database</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>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>SIRS Editorial</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Cytogenetic and genome research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cross, J.G.R.</au><au>Harrison, G.A.</au><au>Coggill, P.</au><au>Sims, S.</au><au>Beck, S.</au><au>Deakin, J.E.</au><au>Marshall Graves, J.A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analysis of the genomic region containing the tammar wallaby (Macropus eugenii) orthologues of MHC class III genes</atitle><jtitle>Cytogenetic and genome research</jtitle><addtitle>Cytogenet Genome Res</addtitle><date>2005-01-01</date><risdate>2005</risdate><volume>111</volume><issue>2</issue><spage>110</spage><epage>117</epage><pages>110-117</pages><issn>1424-8581</issn><eissn>1424-859X</eissn><abstract>Major histocompatibility complex (MHC) molecules are central to development and regulation of the immune system in all jawed vertebrates. MHC class III cytokine genes from the tumor necrosis factor core family, including tumor necrosis factor (TNF) and lymphotoxin alpha and beta (LTA, LTB), are well studied in human and mouse. Orthologues have been identified in several other eutherian species and the cDNA sequences have been reported for a model marsupial, the tammar wallaby. Comparative genomics can help to determine gene function, to understand the evolution of a gene or gene family, and to identify potential regulatory regions. We therefore cloned the genomic region containing the tammar LTB, TNF, and LTA orthologues by “genome walking”, using primers designed from known tammar sequences and regions conserved in other species. We isolated two tammar BAC clones containing all three genes. These tammar genes show similar intergenic distances and the same transcriptional orientation as in human and mouse. Gene structures and sequences are also very conserved. By comparing the tammar, human and mouse genomic sequences we were able to identify candidate regulatory regions for these genes in mammals. Full length sequencing of BACs containing the three genes has been partially completed, and reveals the presence of a number of other tammar MHC III orthologues in this region. </abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>16103651</pmid><doi>10.1159/000086379</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Base Sequence Chromosome Mapping Chromosomes, Artificial, Bacterial Chromosomes, Mammalian Cloning, Molecular Conserved Sequence DNA Primers Genome Humans Macropodidae - genetics Macropodidae - immunology Macropus eugenii Major Histocompatibility Complex Mice Molecular Sequence Data Original Article Polymerase Chain Reaction - methods Sequence Alignment Sequence Homology, Nucleic Acid Transcription, Genetic Tumor Necrosis Factor-alpha - genetics |
title | Analysis of the genomic region containing the tammar wallaby (Macropus eugenii) orthologues of MHC class III genes |
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