Shortening tobacco life cycle accelerates functional gene identification in genomic research.
Identifieur interne : 002918 ( Main/Exploration ); précédent : 002917; suivant : 002919Shortening tobacco life cycle accelerates functional gene identification in genomic research.
Auteurs : G. Ning [République populaire de Chine] ; X. Xiao ; H. Lv ; X. Li ; Y. Zuo ; M. BaoSource :
- Plant biology (Stuttgart, Germany) [ 1438-8677 ] ; 2012.
Descripteurs français
- KwdFr :
- Arabidopsis (croissance et développement), Arabidopsis (génétique), Arabidopsis (métabolisme), Autofécondation (MeSH), Betula (génétique), Clonage moléculaire (MeSH), Croisement consanguin (MeSH), Croisements génétiques (MeSH), Facteurs temps (MeSH), Fleurs (croissance et développement), Fleurs (génétique), Fleurs (métabolisme), Gènes de plante (MeSH), Gènes rapporteurs (MeSH), Génomique (méthodes), Phénotype (MeSH), Plasmides (génétique), Populus (génétique), Protéines d'Arabidopsis (génétique), Protéines d'Arabidopsis (métabolisme), Protéines proto-oncogènes c-myb (génétique), Protéines proto-oncogènes c-myb (métabolisme), Prunus (génétique), Prunus (métabolisme), Régions promotrices (génétique) (MeSH), Régulation de l'expression des gènes végétaux (MeSH), Spécificité d'espèce (MeSH), Tabac (croissance et développement), Tabac (génétique), Tabac (métabolisme), Transformation génétique (MeSH), Végétaux génétiquement modifiés (croissance et développement), Végétaux génétiquement modifiés (génétique), Végétaux génétiquement modifiés (métabolisme).
- MESH :
- croissance et développement : Arabidopsis, Fleurs, Tabac, Végétaux génétiquement modifiés.
- génétique : Arabidopsis, Betula, Fleurs, Plasmides, Populus, Protéines d'Arabidopsis, Protéines proto-oncogènes c-myb, Prunus, Tabac, Végétaux génétiquement modifiés.
- métabolisme : Arabidopsis, Fleurs, Protéines d'Arabidopsis, Protéines proto-oncogènes c-myb, Prunus, Tabac, Végétaux génétiquement modifiés.
- méthodes : Génomique.
- Autofécondation, Clonage moléculaire, Croisement consanguin, Croisements génétiques, Facteurs temps, Gènes de plante, Gènes rapporteurs, Phénotype, Régions promotrices (génétique), Régulation de l'expression des gènes végétaux, Spécificité d'espèce, Transformation génétique.
English descriptors
- KwdEn :
- Arabidopsis (genetics), Arabidopsis (growth & development), Arabidopsis (metabolism), Arabidopsis Proteins (genetics), Arabidopsis Proteins (metabolism), Betula (genetics), Cloning, Molecular (MeSH), Crosses, Genetic (MeSH), Flowers (genetics), Flowers (growth & development), Flowers (metabolism), Gene Expression Regulation, Plant (MeSH), Genes, Plant (MeSH), Genes, Reporter (MeSH), Genomics (methods), Inbreeding (MeSH), Phenotype (MeSH), Plants, Genetically Modified (genetics), Plants, Genetically Modified (growth & development), Plants, Genetically Modified (metabolism), Plasmids (genetics), Populus (genetics), Promoter Regions, Genetic (MeSH), Proto-Oncogene Proteins c-myb (genetics), Proto-Oncogene Proteins c-myb (metabolism), Prunus (genetics), Prunus (metabolism), Self-Fertilization (MeSH), Species Specificity (MeSH), Time Factors (MeSH), Tobacco (genetics), Tobacco (growth & development), Tobacco (metabolism), Transformation, Genetic (MeSH).
- MESH :
- chemical , genetics : Arabidopsis Proteins, Proto-Oncogene Proteins c-myb.
- genetics : Arabidopsis, Betula, Flowers, Plants, Genetically Modified, Plasmids, Populus, Prunus, Tobacco.
- growth & development : Arabidopsis, Flowers, Plants, Genetically Modified, Tobacco.
- metabolism : Arabidopsis, Arabidopsis Proteins, Flowers, Plants, Genetically Modified, Proto-Oncogene Proteins c-myb, Prunus, Tobacco.
- methods : Genomics.
- Cloning, Molecular, Crosses, Genetic, Gene Expression Regulation, Plant, Genes, Plant, Genes, Reporter, Inbreeding, Phenotype, Promoter Regions, Genetic, Self-Fertilization, Species Specificity, Time Factors, Transformation, Genetic.
Abstract
Definitive allocation of function requires the introduction of genetic mutations and analysis of their phenotypic consequences. Novel, rapid and convenient techniques or materials are very important and useful to accelerate gene identification in functional genomics research. Here, over-expression of PmFT (Prunus mume), a novel FT orthologue, and PtFT (Populus tremula) lead to shortening of the tobacco life cycle. A series of novel short life cycle stable tobacco lines (30-50 days) were developed through repeated self-crossing selection breeding. Based on the second transformation via a gusA reporter gene, the promoter from BpFULL1 in silver birch (Betula pendula) and the gene (CPC) from Arabidopsis thaliana were effectively tested using short life cycle tobacco lines. Comparative analysis among wild type, short life cycle tobacco and Arabidopsis transformation system verified that it is optional to accelerate functional gene studies by shortening host plant material life cycle, at least in these short life cycle tobacco lines. The results verified that the novel short life cycle transgenic tobacco lines not only combine the advantages of economic nursery requirements and a simple transformation system, but also provide a robust, effective and stable host system to accelerate gene analysis. Thus, shortening tobacco life cycle strategy is feasible to accelerate heterologous or homologous functional gene identification in genomic research.
DOI: 10.1111/j.1438-8677.2012.00571.x
PubMed: 23107371
Affiliations:
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génétique</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Definitive allocation of function requires the introduction of genetic mutations and analysis of their phenotypic consequences. Novel, rapid and convenient techniques or materials are very important and useful to accelerate gene identification in functional genomics research. Here, over-expression of PmFT (Prunus mume), a novel FT orthologue, and PtFT (Populus tremula) lead to shortening of the tobacco life cycle. A series of novel short life cycle stable tobacco lines (30-50 days) were developed through repeated self-crossing selection breeding. Based on the second transformation via a gusA reporter gene, the promoter from BpFULL1 in silver birch (Betula pendula) and the gene (CPC) from Arabidopsis thaliana were effectively tested using short life cycle tobacco lines. Comparative analysis among wild type, short life cycle tobacco and Arabidopsis transformation system verified that it is optional to accelerate functional gene studies by shortening host plant material life cycle, at least in these short life cycle tobacco lines. The results verified that the novel short life cycle transgenic tobacco lines not only combine the advantages of economic nursery requirements and a simple transformation system, but also provide a robust, effective and stable host system to accelerate gene analysis. Thus, shortening tobacco life cycle strategy is feasible to accelerate heterologous or homologous functional gene identification in genomic research.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">23107371</PMID><DateCompleted><Year>2013</Year><Month>03</Month><Day>28</Day></DateCompleted><DateRevised><Year>2012</Year><Month>10</Month><Day>30</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1438-8677</ISSN><JournalIssue CitedMedium="Internet"><Volume>14</Volume><Issue>6</Issue><PubDate><Year>2012</Year><Month>Nov</Month></PubDate></JournalIssue><Title>Plant biology (Stuttgart, Germany)</Title><ISOAbbreviation>Plant Biol (Stuttg)</ISOAbbreviation></Journal><ArticleTitle>Shortening tobacco life cycle accelerates functional gene identification in genomic research.</ArticleTitle><Pagination><MedlinePgn>934-43</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1111/j.1438-8677.2012.00571.x</ELocationID><Abstract><AbstractText>Definitive allocation of function requires the introduction of genetic mutations and analysis of their phenotypic consequences. Novel, rapid and convenient techniques or materials are very important and useful to accelerate gene identification in functional genomics research. Here, over-expression of PmFT (Prunus mume), a novel FT orthologue, and PtFT (Populus tremula) lead to shortening of the tobacco life cycle. A series of novel short life cycle stable tobacco lines (30-50 days) were developed through repeated self-crossing selection breeding. Based on the second transformation via a gusA reporter gene, the promoter from BpFULL1 in silver birch (Betula pendula) and the gene (CPC) from Arabidopsis thaliana were effectively tested using short life cycle tobacco lines. Comparative analysis among wild type, short life cycle tobacco and Arabidopsis transformation system verified that it is optional to accelerate functional gene studies by shortening host plant material life cycle, at least in these short life cycle tobacco lines. The results verified that the novel short life cycle transgenic tobacco lines not only combine the advantages of economic nursery requirements and a simple transformation system, but also provide a robust, effective and stable host system to accelerate gene analysis. Thus, shortening tobacco life cycle strategy is feasible to accelerate heterologous or homologous functional gene identification in genomic research.</AbstractText><CopyrightInformation>© 2012 German Botanical Society and The Royal Botanical Society of the Netherlands.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Ning</LastName><ForeName>G</ForeName><Initials>G</Initials><AffiliationInfo><Affiliation>Key laboratory of Horticultural Plant Biology, Ministry of Education, College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Xiao</LastName><ForeName>X</ForeName><Initials>X</Initials></Author><Author ValidYN="Y"><LastName>Lv</LastName><ForeName>H</ForeName><Initials>H</Initials></Author><Author ValidYN="Y"><LastName>Li</LastName><ForeName>X</ForeName><Initials>X</Initials></Author><Author ValidYN="Y"><LastName>Zuo</LastName><ForeName>Y</ForeName><Initials>Y</Initials></Author><Author ValidYN="Y"><LastName>Bao</LastName><ForeName>M</ForeName><Initials>M</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2012</Year><Month>03</Month><Day>26</Day></ArticleDate></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>Plant Biol (Stuttg)</MedlineTA><NlmUniqueID>101148926</NlmUniqueID><ISSNLinking>1435-8603</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D029681">Arabidopsis Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="C511989">CPC protein, Arabidopsis</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D020598">Proto-Oncogene Proteins c-myb</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D017360" MajorTopicYN="N">Arabidopsis</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000254" MajorTopicYN="N">growth & development</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D029681" MajorTopicYN="N">Arabidopsis Proteins</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D029662" MajorTopicYN="N">Betula</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003001" MajorTopicYN="N">Cloning, Molecular</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D003433" MajorTopicYN="N">Crosses, Genetic</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D035264" MajorTopicYN="N">Flowers</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000254" MajorTopicYN="N">growth & development</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018506" MajorTopicYN="Y">Gene Expression Regulation, Plant</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D017343" MajorTopicYN="Y">Genes, Plant</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D017930" MajorTopicYN="N">Genes, Reporter</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D023281" MajorTopicYN="N">Genomics</DescriptorName><QualifierName UI="Q000379" MajorTopicYN="Y">methods</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D007178" MajorTopicYN="N">Inbreeding</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D010641" MajorTopicYN="N">Phenotype</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D030821" MajorTopicYN="N">Plants, Genetically Modified</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000254" MajorTopicYN="N">growth & development</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010957" MajorTopicYN="N">Plasmids</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D032107" MajorTopicYN="N">Populus</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D011401" MajorTopicYN="N">Promoter Regions, Genetic</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D020598" MajorTopicYN="N">Proto-Oncogene Proteins c-myb</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D027861" MajorTopicYN="N">Prunus</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D057945" MajorTopicYN="N">Self-Fertilization</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D013045" MajorTopicYN="N">Species Specificity</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D013997" MajorTopicYN="N">Time Factors</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D014026" MajorTopicYN="N">Tobacco</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName><QualifierName UI="Q000254" MajorTopicYN="N">growth & development</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D014170" MajorTopicYN="N">Transformation, Genetic</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2012</Year><Month>10</Month><Day>31</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2012</Year><Month>10</Month><Day>31</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2013</Year><Month>3</Month><Day>30</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">23107371</ArticleId><ArticleId IdType="doi">10.1111/j.1438-8677.2012.00571.x</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>République populaire de Chine</li></country><region><li>Hubei</li></region><settlement><li>Wuhan</li></settlement></list><tree><noCountry><name sortKey="Bao, M" sort="Bao, M" uniqKey="Bao M" first="M" last="Bao">M. Bao</name><name sortKey="Li, X" sort="Li, X" uniqKey="Li X" first="X" last="Li">X. Li</name><name sortKey="Lv, H" sort="Lv, H" uniqKey="Lv H" first="H" last="Lv">H. Lv</name><name sortKey="Xiao, X" sort="Xiao, X" uniqKey="Xiao X" first="X" last="Xiao">X. Xiao</name><name sortKey="Zuo, Y" sort="Zuo, Y" uniqKey="Zuo Y" first="Y" last="Zuo">Y. Zuo</name></noCountry><country name="République populaire de Chine"><region name="Hubei"><name sortKey="Ning, G" sort="Ning, G" uniqKey="Ning G" first="G" last="Ning">G. Ning</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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