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Using de novo genome assembly and high-throughput sequencing to characterize the MHC region in a non-model bird, the Eurasian coot
Genes of the Major Histocompatibility Complex (MHC) form a key component of vertebrate adaptive immunity, as they code for molecules which bind antigens of intra- and extracellular pathogens (MHC class I and II, respectively) and present them to T cell receptors. In general, MHC genes are hyper-poly...
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Published in: | Scientific reports 2022-04, Vol.12 (1), p.7031-7031, Article 7031 |
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description | Genes of the Major Histocompatibility Complex (MHC) form a key component of vertebrate adaptive immunity, as they code for molecules which bind antigens of intra- and extracellular pathogens (MHC class I and II, respectively) and present them to T cell receptors. In general, MHC genes are hyper-polymorphic and high MHC diversity is often maintained within natural populations (via balancing selection) and within individuals (via gene duplications). Because of its complex architecture with tandems of duplicated genes, characterization of MHC region in non-model vertebrate species still poses a major challenge. Here, we combined de novo genome assembly and high-throughput sequencing to characterize MHC polymorphism in a rallid bird species, the Eurasian coot
Fulica atra
. An analysis of genome assembly indicated high duplication rate at MHC-I, which was also supported by targeted sequencing of peptide-binding exons (at least five MHC-I loci genotyped). We found high allelic richness at both MHC-I and MHC-II, although signature of diversifying selection and recombination (gene conversion) was much stronger at MHC-II. Our results indicate that Eurasian coot retains extraordinary polymorphism at both MHC classes (when compared to other non-passerine bird species), although they may be subject to different evolutionary mechanism. |
doi_str_mv | 10.1038/s41598-022-11018-w |
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Fulica atra
. An analysis of genome assembly indicated high duplication rate at MHC-I, which was also supported by targeted sequencing of peptide-binding exons (at least five MHC-I loci genotyped). We found high allelic richness at both MHC-I and MHC-II, although signature of diversifying selection and recombination (gene conversion) was much stronger at MHC-II. Our results indicate that Eurasian coot retains extraordinary polymorphism at both MHC classes (when compared to other non-passerine bird species), although they may be subject to different evolutionary mechanism.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-022-11018-w</identifier><identifier>PMID: 35488050</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/181 ; 631/208 ; 631/250 ; Adaptive immunity ; Animals ; Antigens ; Birds ; Birds - genetics ; Exons ; Gene conversion ; Gene Duplication ; Genes ; Genomes ; High-Throughput Nucleotide Sequencing ; Humanities and Social Sciences ; Humans ; Lymphocytes T ; Major histocompatibility complex ; Major Histocompatibility Complex - genetics ; multidisciplinary ; Natural populations ; Next-generation sequencing ; Phylogeny ; Polymorphism ; Recombination ; Science ; Science (multidisciplinary) ; Species ; T cell receptors ; Vertebrates</subject><ispartof>Scientific reports, 2022-04, Vol.12 (1), p.7031-7031, Article 7031</ispartof><rights>The Author(s) 2022</rights><rights>2022. The Author(s).</rights><rights>The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c421t-7fe1f9ce2cad7bc1920e901c80346ac09b3949f66a1eadd30921136bd2b9671b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2656988500/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2656988500?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35488050$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pikus, Ewa</creatorcontrib><creatorcontrib>Minias, Piotr</creatorcontrib><title>Using de novo genome assembly and high-throughput sequencing to characterize the MHC region in a non-model bird, the Eurasian coot</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Genes of the Major Histocompatibility Complex (MHC) form a key component of vertebrate adaptive immunity, as they code for molecules which bind antigens of intra- and extracellular pathogens (MHC class I and II, respectively) and present them to T cell receptors. In general, MHC genes are hyper-polymorphic and high MHC diversity is often maintained within natural populations (via balancing selection) and within individuals (via gene duplications). Because of its complex architecture with tandems of duplicated genes, characterization of MHC region in non-model vertebrate species still poses a major challenge. Here, we combined de novo genome assembly and high-throughput sequencing to characterize MHC polymorphism in a rallid bird species, the Eurasian coot
Fulica atra
. An analysis of genome assembly indicated high duplication rate at MHC-I, which was also supported by targeted sequencing of peptide-binding exons (at least five MHC-I loci genotyped). We found high allelic richness at both MHC-I and MHC-II, although signature of diversifying selection and recombination (gene conversion) was much stronger at MHC-II. Our results indicate that Eurasian coot retains extraordinary polymorphism at both MHC classes (when compared to other non-passerine bird species), although they may be subject to different evolutionary mechanism.</description><subject>631/181</subject><subject>631/208</subject><subject>631/250</subject><subject>Adaptive immunity</subject><subject>Animals</subject><subject>Antigens</subject><subject>Birds</subject><subject>Birds - genetics</subject><subject>Exons</subject><subject>Gene conversion</subject><subject>Gene Duplication</subject><subject>Genes</subject><subject>Genomes</subject><subject>High-Throughput Nucleotide Sequencing</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Lymphocytes T</subject><subject>Major histocompatibility complex</subject><subject>Major Histocompatibility Complex - genetics</subject><subject>multidisciplinary</subject><subject>Natural populations</subject><subject>Next-generation sequencing</subject><subject>Phylogeny</subject><subject>Polymorphism</subject><subject>Recombination</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Species</subject><subject>T cell receptors</subject><subject>Vertebrates</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9ks1u1DAURiMEotXQF2CBLLFhQcB_SewNEhq1tFIRG7q2HOcm8SixB9tp1S558npmSmlZ4I0t-9xj--orircEfyKYic-Rk0qKElNaEoKJKG9eFMcU86qkjNKXT9ZHxUmMG5xHRSUn8nVxxCouBK7wcfH7Klo3oA6Q89ceDeD8DEjHCHM73SLtOjTaYSzTGPwyjNsloQi_FnBmV5Y8MqMO2iQI9g5QGgF9P1-jAIP1DlmHdPa6cvYdTKi1ofu4Z06XoKPVDhnv05viVa-nCCcP86q4Ojv9uT4vL398u1h_vSwNpySVTQ-klwao0V3TGiIpBomJEZjxWhssWya57OtaE9Bdx7CkhLC67Wgr64a0bFVcHLyd1xu1DXbW4VZ5bdV-w4dB6ZCsmUCBEVxw1jY1MJ6bJqURVU8r3giKWdauii8H13ZpZ-gMuBT09Ez6_MTZUQ3-WkmcW0-qLPjwIAg-tzMmNdtoYJq0A79ERetKUFoLukPf_4Nu_BJcbtWOqqUQFcaZogfKBB9jgP7xMQSrXWLUITEqJ0btE6NuctG7p994LPmTjwywAxDzkRsg_L37P9p7Dx7MdQ</recordid><startdate>20220429</startdate><enddate>20220429</enddate><creator>Pikus, Ewa</creator><creator>Minias, Piotr</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><general>Nature Portfolio</general><scope>C6C</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20220429</creationdate><title>Using de novo genome assembly and high-throughput sequencing to characterize the MHC region in a non-model bird, the Eurasian coot</title><author>Pikus, Ewa ; Minias, Piotr</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-7fe1f9ce2cad7bc1920e901c80346ac09b3949f66a1eadd30921136bd2b9671b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>631/181</topic><topic>631/208</topic><topic>631/250</topic><topic>Adaptive immunity</topic><topic>Animals</topic><topic>Antigens</topic><topic>Birds</topic><topic>Birds - genetics</topic><topic>Exons</topic><topic>Gene conversion</topic><topic>Gene Duplication</topic><topic>Genes</topic><topic>Genomes</topic><topic>High-Throughput Nucleotide Sequencing</topic><topic>Humanities and Social Sciences</topic><topic>Humans</topic><topic>Lymphocytes T</topic><topic>Major histocompatibility complex</topic><topic>Major Histocompatibility Complex - genetics</topic><topic>multidisciplinary</topic><topic>Natural populations</topic><topic>Next-generation sequencing</topic><topic>Phylogeny</topic><topic>Polymorphism</topic><topic>Recombination</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Species</topic><topic>T cell receptors</topic><topic>Vertebrates</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pikus, Ewa</creatorcontrib><creatorcontrib>Minias, Piotr</creatorcontrib><collection>Springer Nature OA Free Journals</collection><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>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>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>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>Publicly Available Content Database</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 Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pikus, Ewa</au><au>Minias, Piotr</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Using de novo genome assembly and high-throughput sequencing to characterize the MHC region in a non-model bird, the Eurasian coot</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2022-04-29</date><risdate>2022</risdate><volume>12</volume><issue>1</issue><spage>7031</spage><epage>7031</epage><pages>7031-7031</pages><artnum>7031</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Genes of the Major Histocompatibility Complex (MHC) form a key component of vertebrate adaptive immunity, as they code for molecules which bind antigens of intra- and extracellular pathogens (MHC class I and II, respectively) and present them to T cell receptors. In general, MHC genes are hyper-polymorphic and high MHC diversity is often maintained within natural populations (via balancing selection) and within individuals (via gene duplications). Because of its complex architecture with tandems of duplicated genes, characterization of MHC region in non-model vertebrate species still poses a major challenge. Here, we combined de novo genome assembly and high-throughput sequencing to characterize MHC polymorphism in a rallid bird species, the Eurasian coot
Fulica atra
. An analysis of genome assembly indicated high duplication rate at MHC-I, which was also supported by targeted sequencing of peptide-binding exons (at least five MHC-I loci genotyped). We found high allelic richness at both MHC-I and MHC-II, although signature of diversifying selection and recombination (gene conversion) was much stronger at MHC-II. Our results indicate that Eurasian coot retains extraordinary polymorphism at both MHC classes (when compared to other non-passerine bird species), although they may be subject to different evolutionary mechanism.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>35488050</pmid><doi>10.1038/s41598-022-11018-w</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 631/181 631/208 631/250 Adaptive immunity Animals Antigens Birds Birds - genetics Exons Gene conversion Gene Duplication Genes Genomes High-Throughput Nucleotide Sequencing Humanities and Social Sciences Humans Lymphocytes T Major histocompatibility complex Major Histocompatibility Complex - genetics multidisciplinary Natural populations Next-generation sequencing Phylogeny Polymorphism Recombination Science Science (multidisciplinary) Species T cell receptors Vertebrates |
title | Using de novo genome assembly and high-throughput sequencing to characterize the MHC region in a non-model bird, the Eurasian coot |
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