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Comprehensive genomic analysis of the CNGC gene family in Brassica oleracea: novel insights into synteny, structures, and transcript profiles
The cyclic nucleotide-gated ion channel (CNGC) family affects the uptake of cations, growth, pathogen defence, and thermotolerance in plants. However, the systematic identification, origin and function of this gene family has not been performed in Brassica oleracea, an important vegetable crop and g...
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Published in: | BMC genomics 2017-11, Vol.18 (1), p.869-869, Article 869 |
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description | The cyclic nucleotide-gated ion channel (CNGC) family affects the uptake of cations, growth, pathogen defence, and thermotolerance in plants. However, the systematic identification, origin and function of this gene family has not been performed in Brassica oleracea, an important vegetable crop and genomic model organism.
In present study, we identified 26 CNGC genes in B. oleracea genome, which are non-randomly localized on eight chromosomes, and classified into four major (I-IV) and two sub-groups (i.e., IV-a and IV-b). The BoCNGC family is asymmetrically fractioned into the following three sub-genomes: least fractionated (14 genes), most fractionated-I (10), and most fractionated-II (2). The syntenic map of BoCNGC genes exhibited strong relationships with the model Arabidopsis thaliana and B. rapa CNGC genes and provided markers for defining the regions of conserved synteny among the three genomes. Both whole-genome triplication along with segmental and tandem duplications contributed to the expansion of this gene family. We predicted the characteristics of BoCNGCs regarding exon-intron organisations, motif compositions and post-translational modifications, which diversified their structures and functions. Using orthologous Arabidopsis CNGCs as a reference, we found that most CNGCs were associated with various protein-protein interaction networks involving CNGCs and other signalling and stress related proteins. We revealed that five microRNAs (i.e., bol-miR5021, bol-miR838d, bol-miR414b, bol-miR4234, and bol-miR_new2) have target sites in nine BoCNGC genes. The BoCNGC genes were differentially expressed in seven B. oleracea tissues including leaf, stem, callus, silique, bud, root and flower. The transcript abundance levels quantified by qRT-PCR assays revealed that BoCNGC genes from phylogenetic Groups I and IV were particularly sensitive to cold stress and infections with bacterial pathogen Xanthomonas campestris pv. campestris, suggesting their importance in abiotic and biotic stress responses.
Our comprehensive genome-wide analysis represents a rich data resource for studying new plant gene families. Our data may also be useful for breeding new B. oleracea cultivars with improved productivity, quality, and stress resistance. |
doi_str_mv | 10.1186/s12864-017-4244-y |
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In present study, we identified 26 CNGC genes in B. oleracea genome, which are non-randomly localized on eight chromosomes, and classified into four major (I-IV) and two sub-groups (i.e., IV-a and IV-b). The BoCNGC family is asymmetrically fractioned into the following three sub-genomes: least fractionated (14 genes), most fractionated-I (10), and most fractionated-II (2). The syntenic map of BoCNGC genes exhibited strong relationships with the model Arabidopsis thaliana and B. rapa CNGC genes and provided markers for defining the regions of conserved synteny among the three genomes. Both whole-genome triplication along with segmental and tandem duplications contributed to the expansion of this gene family. We predicted the characteristics of BoCNGCs regarding exon-intron organisations, motif compositions and post-translational modifications, which diversified their structures and functions. Using orthologous Arabidopsis CNGCs as a reference, we found that most CNGCs were associated with various protein-protein interaction networks involving CNGCs and other signalling and stress related proteins. We revealed that five microRNAs (i.e., bol-miR5021, bol-miR838d, bol-miR414b, bol-miR4234, and bol-miR_new2) have target sites in nine BoCNGC genes. The BoCNGC genes were differentially expressed in seven B. oleracea tissues including leaf, stem, callus, silique, bud, root and flower. The transcript abundance levels quantified by qRT-PCR assays revealed that BoCNGC genes from phylogenetic Groups I and IV were particularly sensitive to cold stress and infections with bacterial pathogen Xanthomonas campestris pv. campestris, suggesting their importance in abiotic and biotic stress responses.
Our comprehensive genome-wide analysis represents a rich data resource for studying new plant gene families. Our data may also be useful for breeding new B. oleracea cultivars with improved productivity, quality, and stress resistance.</description><identifier>ISSN: 1471-2164</identifier><identifier>EISSN: 1471-2164</identifier><identifier>DOI: 10.1186/s12864-017-4244-y</identifier><identifier>PMID: 29132315</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Abiotic and biotic stress ; Abiotic stress ; Amino acids ; Arabidopsis thaliana ; Brassica ; Brassica oleracea ; Callus ; Cations ; Chromosomes ; CNGC ; Cultivars ; Evolution ; Evolutionary conservation ; Expression pattern ; Flowers & plants ; Gene expression ; Gene families ; Genes ; Genomes ; Genomic analysis ; Genomics ; Ion channels ; miRNA ; Nucleotides ; Pathogens ; Phylogenetics ; Phylogeny ; Physiology ; Plant breeding ; Plant genetics ; Post-translation ; Protein-protein interactions ; Proteins ; Signal transduction ; Synteny ; Temperature tolerance ; Transcription ; Vegetables</subject><ispartof>BMC genomics, 2017-11, Vol.18 (1), p.869-869, Article 869</ispartof><rights>COPYRIGHT 2017 BioMed Central Ltd.</rights><rights>2017. This work is licensed 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><rights>The Author(s). 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c594t-8d1bd3118b06f36631d2435b5b47fecbeef9b812826831b8086d971d4ab067053</citedby><cites>FETCH-LOGICAL-c594t-8d1bd3118b06f36631d2435b5b47fecbeef9b812826831b8086d971d4ab067053</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5683364/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2348379726?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29132315$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kakar, Kaleem U</creatorcontrib><creatorcontrib>Nawaz, Zarqa</creatorcontrib><creatorcontrib>Kakar, Khadija</creatorcontrib><creatorcontrib>Ali, Essa</creatorcontrib><creatorcontrib>Almoneafy, Abdulwareth A</creatorcontrib><creatorcontrib>Ullah, Raqeeb</creatorcontrib><creatorcontrib>Ren, Xue-Liang</creatorcontrib><creatorcontrib>Shu, Qing-Yao</creatorcontrib><title>Comprehensive genomic analysis of the CNGC gene family in Brassica oleracea: novel insights into synteny, structures, and transcript profiles</title><title>BMC genomics</title><addtitle>BMC Genomics</addtitle><description>The cyclic nucleotide-gated ion channel (CNGC) family affects the uptake of cations, growth, pathogen defence, and thermotolerance in plants. However, the systematic identification, origin and function of this gene family has not been performed in Brassica oleracea, an important vegetable crop and genomic model organism.
In present study, we identified 26 CNGC genes in B. oleracea genome, which are non-randomly localized on eight chromosomes, and classified into four major (I-IV) and two sub-groups (i.e., IV-a and IV-b). The BoCNGC family is asymmetrically fractioned into the following three sub-genomes: least fractionated (14 genes), most fractionated-I (10), and most fractionated-II (2). The syntenic map of BoCNGC genes exhibited strong relationships with the model Arabidopsis thaliana and B. rapa CNGC genes and provided markers for defining the regions of conserved synteny among the three genomes. Both whole-genome triplication along with segmental and tandem duplications contributed to the expansion of this gene family. We predicted the characteristics of BoCNGCs regarding exon-intron organisations, motif compositions and post-translational modifications, which diversified their structures and functions. Using orthologous Arabidopsis CNGCs as a reference, we found that most CNGCs were associated with various protein-protein interaction networks involving CNGCs and other signalling and stress related proteins. We revealed that five microRNAs (i.e., bol-miR5021, bol-miR838d, bol-miR414b, bol-miR4234, and bol-miR_new2) have target sites in nine BoCNGC genes. The BoCNGC genes were differentially expressed in seven B. oleracea tissues including leaf, stem, callus, silique, bud, root and flower. The transcript abundance levels quantified by qRT-PCR assays revealed that BoCNGC genes from phylogenetic Groups I and IV were particularly sensitive to cold stress and infections with bacterial pathogen Xanthomonas campestris pv. campestris, suggesting their importance in abiotic and biotic stress responses.
Our comprehensive genome-wide analysis represents a rich data resource for studying new plant gene families. Our data may also be useful for breeding new B. oleracea cultivars with improved productivity, quality, and stress resistance.</description><subject>Abiotic and biotic stress</subject><subject>Abiotic stress</subject><subject>Amino acids</subject><subject>Arabidopsis thaliana</subject><subject>Brassica</subject><subject>Brassica oleracea</subject><subject>Callus</subject><subject>Cations</subject><subject>Chromosomes</subject><subject>CNGC</subject><subject>Cultivars</subject><subject>Evolution</subject><subject>Evolutionary conservation</subject><subject>Expression pattern</subject><subject>Flowers & plants</subject><subject>Gene expression</subject><subject>Gene families</subject><subject>Genes</subject><subject>Genomes</subject><subject>Genomic analysis</subject><subject>Genomics</subject><subject>Ion channels</subject><subject>miRNA</subject><subject>Nucleotides</subject><subject>Pathogens</subject><subject>Phylogenetics</subject><subject>Phylogeny</subject><subject>Physiology</subject><subject>Plant breeding</subject><subject>Plant genetics</subject><subject>Post-translation</subject><subject>Protein-protein interactions</subject><subject>Proteins</subject><subject>Signal transduction</subject><subject>Synteny</subject><subject>Temperature tolerance</subject><subject>Transcription</subject><subject>Vegetables</subject><issn>1471-2164</issn><issn>1471-2164</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkt-K1DAYxYso7rr6AN5IwBuF7Zo0adp6IayDrgOLgn-uQ5J-7WRokzFJB_sQvrOps647Ir1o6Pc7J83JybKnBF8QUvNXgRQ1ZzkmVc4KxvL5XnZKWEXygnB2_876JHsUwhYnsC7Kh9lJ0RBaUFKeZj9Xbtx52IANZg-oB-tGo5G0cpiDCch1KG4ArT5erZYhoE6OZpiRseitlyEYLZEbwEsN8jWybg9DmgXTb2JIi-hQmG0EO5-jEP2k4-QhnCf_FkUvbdDe7CLaedeZAcLj7EEnhwBPbt5n2bf3776uPuTXn67Wq8vrXJcNi3ndEtXSFIHCvKOcU9IWjJaqVKzqQCuArlF1CqfgNSWqxjVvm4q0TCZBhUt6lq0Pvq2TW7HzZpR-Fk4a8fuD872QPho9gFAcg2Qd5opJlkJXWleqo6WUTdt0WiWvNwev3aRGaDXYdLDhyPR4Ys1G9G4vyvRzlLNk8OLGwLvvE4QoRhM0DIO04KYgSMNZUeGmrhL6_B906yaf7iqIgrKaVk1V8L9UL9MBjO1c2lcvpuKyZBxXGNOFuvgPlZ4WUgOcheVGjgUvjwSJifAj9nIKQay_fD5myYHV3oXgobvNg2CxdFccuitSJcXSXTEnzbO7Qd4q_pSV_gJI2Oqw</recordid><startdate>20171113</startdate><enddate>20171113</enddate><creator>Kakar, 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genomic analysis of the CNGC gene family in Brassica oleracea: novel insights into synteny, structures, and transcript profiles</title><author>Kakar, Kaleem U ; Nawaz, Zarqa ; Kakar, Khadija ; Ali, Essa ; Almoneafy, Abdulwareth A ; Ullah, Raqeeb ; Ren, Xue-Liang ; Shu, Qing-Yao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c594t-8d1bd3118b06f36631d2435b5b47fecbeef9b812826831b8086d971d4ab067053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Abiotic and biotic stress</topic><topic>Abiotic stress</topic><topic>Amino acids</topic><topic>Arabidopsis thaliana</topic><topic>Brassica</topic><topic>Brassica oleracea</topic><topic>Callus</topic><topic>Cations</topic><topic>Chromosomes</topic><topic>CNGC</topic><topic>Cultivars</topic><topic>Evolution</topic><topic>Evolutionary conservation</topic><topic>Expression pattern</topic><topic>Flowers & plants</topic><topic>Gene expression</topic><topic>Gene families</topic><topic>Genes</topic><topic>Genomes</topic><topic>Genomic analysis</topic><topic>Genomics</topic><topic>Ion channels</topic><topic>miRNA</topic><topic>Nucleotides</topic><topic>Pathogens</topic><topic>Phylogenetics</topic><topic>Phylogeny</topic><topic>Physiology</topic><topic>Plant breeding</topic><topic>Plant genetics</topic><topic>Post-translation</topic><topic>Protein-protein interactions</topic><topic>Proteins</topic><topic>Signal transduction</topic><topic>Synteny</topic><topic>Temperature tolerance</topic><topic>Transcription</topic><topic>Vegetables</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kakar, Kaleem U</creatorcontrib><creatorcontrib>Nawaz, Zarqa</creatorcontrib><creatorcontrib>Kakar, Khadija</creatorcontrib><creatorcontrib>Ali, Essa</creatorcontrib><creatorcontrib>Almoneafy, Abdulwareth A</creatorcontrib><creatorcontrib>Ullah, Raqeeb</creatorcontrib><creatorcontrib>Ren, 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Zarqa</au><au>Kakar, Khadija</au><au>Ali, Essa</au><au>Almoneafy, Abdulwareth A</au><au>Ullah, Raqeeb</au><au>Ren, Xue-Liang</au><au>Shu, Qing-Yao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comprehensive genomic analysis of the CNGC gene family in Brassica oleracea: novel insights into synteny, structures, and transcript profiles</atitle><jtitle>BMC genomics</jtitle><addtitle>BMC Genomics</addtitle><date>2017-11-13</date><risdate>2017</risdate><volume>18</volume><issue>1</issue><spage>869</spage><epage>869</epage><pages>869-869</pages><artnum>869</artnum><issn>1471-2164</issn><eissn>1471-2164</eissn><abstract>The cyclic nucleotide-gated ion channel (CNGC) family affects the uptake of cations, growth, pathogen defence, and thermotolerance in plants. However, the systematic identification, origin and function of this gene family has not been performed in Brassica oleracea, an important vegetable crop and genomic model organism.
In present study, we identified 26 CNGC genes in B. oleracea genome, which are non-randomly localized on eight chromosomes, and classified into four major (I-IV) and two sub-groups (i.e., IV-a and IV-b). The BoCNGC family is asymmetrically fractioned into the following three sub-genomes: least fractionated (14 genes), most fractionated-I (10), and most fractionated-II (2). The syntenic map of BoCNGC genes exhibited strong relationships with the model Arabidopsis thaliana and B. rapa CNGC genes and provided markers for defining the regions of conserved synteny among the three genomes. Both whole-genome triplication along with segmental and tandem duplications contributed to the expansion of this gene family. We predicted the characteristics of BoCNGCs regarding exon-intron organisations, motif compositions and post-translational modifications, which diversified their structures and functions. Using orthologous Arabidopsis CNGCs as a reference, we found that most CNGCs were associated with various protein-protein interaction networks involving CNGCs and other signalling and stress related proteins. We revealed that five microRNAs (i.e., bol-miR5021, bol-miR838d, bol-miR414b, bol-miR4234, and bol-miR_new2) have target sites in nine BoCNGC genes. The BoCNGC genes were differentially expressed in seven B. oleracea tissues including leaf, stem, callus, silique, bud, root and flower. The transcript abundance levels quantified by qRT-PCR assays revealed that BoCNGC genes from phylogenetic Groups I and IV were particularly sensitive to cold stress and infections with bacterial pathogen Xanthomonas campestris pv. campestris, suggesting their importance in abiotic and biotic stress responses.
Our comprehensive genome-wide analysis represents a rich data resource for studying new plant gene families. Our data may also be useful for breeding new B. oleracea cultivars with improved productivity, quality, and stress resistance.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>29132315</pmid><doi>10.1186/s12864-017-4244-y</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Abiotic and biotic stress Abiotic stress Amino acids Arabidopsis thaliana Brassica Brassica oleracea Callus Cations Chromosomes CNGC Cultivars Evolution Evolutionary conservation Expression pattern Flowers & plants Gene expression Gene families Genes Genomes Genomic analysis Genomics Ion channels miRNA Nucleotides Pathogens Phylogenetics Phylogeny Physiology Plant breeding Plant genetics Post-translation Protein-protein interactions Proteins Signal transduction Synteny Temperature tolerance Transcription Vegetables |
title | Comprehensive genomic analysis of the CNGC gene family in Brassica oleracea: novel insights into synteny, structures, and transcript profiles |
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