Expression of an anther-specific chalcone synthase-like gene is correlated with uninucleate microspore development in Nicotiana sylvestris.
Identifieur interne : 002A03 ( Main/Exploration ); précédent : 002A02; suivant : 002A04Expression of an anther-specific chalcone synthase-like gene is correlated with uninucleate microspore development in Nicotiana sylvestris.
Auteurs : I. Atanassov [Bulgarie] ; E. Russinova ; L. Antonov ; A. AtanassovSource :
- Plant molecular biology [ 0167-4412 ] ; 1998.
Descripteurs français
- KwdFr :
- ADN complémentaire (MeSH), Acyltransferases (biosynthèse), Acyltransferases (composition chimique), Acyltransferases (génétique), Alignement de séquences (MeSH), Cadres ouverts de lecture (MeSH), Clonage moléculaire (MeSH), Données de séquences moléculaires (MeSH), Isoenzymes (biosynthèse), Isoenzymes (composition chimique), Isoenzymes (génétique), Phylogenèse (MeSH), Protéines de fusion recombinantes (biosynthèse), Protéines de fusion recombinantes (composition chimique), Régulation de l'expression des gènes codant pour des enzymes (MeSH), Régulation de l'expression des gènes végétaux (MeSH), Similitude de séquences d'acides aminés (MeSH), Spores (MeSH), Séquence d'acides aminés (MeSH), Tabac (enzymologie), Tabac (génétique), Tabac (physiologie), Végétaux toxiques (MeSH), Évolution moléculaire (MeSH).
- MESH :
- biosynthèse : Acyltransferases, Isoenzymes, Protéines de fusion recombinantes.
- composition chimique : Acyltransferases, Isoenzymes, Protéines de fusion recombinantes.
- enzymologie : Tabac.
- génétique : Acyltransferases, Isoenzymes, Tabac.
- physiologie : Tabac.
- ADN complémentaire, Alignement de séquences, Cadres ouverts de lecture, Clonage moléculaire, Données de séquences moléculaires, Phylogenèse, Régulation de l'expression des gènes codant pour des enzymes, Régulation de l'expression des gènes végétaux, Similitude de séquences d'acides aminés, Spores, Séquence d'acides aminés, Végétaux toxiques, Évolution moléculaire.
English descriptors
- KwdEn :
- Acyltransferases (biosynthesis), Acyltransferases (chemistry), Acyltransferases (genetics), Amino Acid Sequence (MeSH), Cloning, Molecular (MeSH), DNA, Complementary (MeSH), Evolution, Molecular (MeSH), Gene Expression Regulation, Enzymologic (MeSH), Gene Expression Regulation, Plant (MeSH), Isoenzymes (biosynthesis), Isoenzymes (chemistry), Isoenzymes (genetics), Molecular Sequence Data (MeSH), Open Reading Frames (MeSH), Phylogeny (MeSH), Plants, Toxic (MeSH), Recombinant Fusion Proteins (biosynthesis), Recombinant Fusion Proteins (chemistry), Sequence Alignment (MeSH), Sequence Homology, Amino Acid (MeSH), Spores (MeSH), Tobacco (enzymology), Tobacco (genetics), Tobacco (physiology).
- MESH :
- chemical , biosynthesis : Acyltransferases, Isoenzymes, Recombinant Fusion Proteins.
- chemical , chemistry : Acyltransferases, Isoenzymes, Recombinant Fusion Proteins.
- chemical , genetics : Acyltransferases, Isoenzymes.
- enzymology : Tobacco.
- genetics : Tobacco.
- physiology : Tobacco.
- Amino Acid Sequence, Cloning, Molecular, DNA, Complementary, Evolution, Molecular, Gene Expression Regulation, Enzymologic, Gene Expression Regulation, Plant, Molecular Sequence Data, Open Reading Frames, Phylogeny, Plants, Toxic, Sequence Alignment, Sequence Homology, Amino Acid, Spores.
Abstract
Two cDNA clones, specifically expressed in Nicotiana sylvestris anthers during uninucleate microspore development, were isolated using a subtractive hybridization approach. Sequence analysis showed that one of them, NSCHSLK, displayed a high level of similarity to several anther-specific chalcone synthase-like (CHSLK) proteins and an ORF from chromosome I of Arabidopsis thaliana. A lower, but significant, similarity to chalcone synthases and closely related enzymes (CHSRE) was also detected. The structure of the nschslk gene was found to be typical of the chalcone (chs)/stilbene (sts) synthase family. Expression of NSCHSLK mRNA was confined to microspores and tapetal cells. UV-irradiation or infection with Phytophthora parasitica var. nicotianae of transgenic Nicotiana benthamiana plants carrying a chimeric nschslk/GUS gene indicated that the nschslk promoter exhibits the same anther-specific, developmentally regulated expression pattern. Comparison of CHSRE and CHSLK polypeptide sequences revealed some important similarities and differences between the two groups. The data presented in this study, suggest that the anther-specific chslk genes represent a separate sub-family of plant polyketide synthases related to chs/sts in terms of gene structure, polypeptide sequence and the possible catalytic mechanism, but differing in substrate/product specificity. The putative role of CHSLK enzymes in anther development and particularly in exine synthesis is discussed.
DOI: 10.1023/a:1006074508779
PubMed: 9869422
Affiliations:
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moléculaire</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Two cDNA clones, specifically expressed in Nicotiana sylvestris anthers during uninucleate microspore development, were isolated using a subtractive hybridization approach. Sequence analysis showed that one of them, NSCHSLK, displayed a high level of similarity to several anther-specific chalcone synthase-like (CHSLK) proteins and an ORF from chromosome I of Arabidopsis thaliana. A lower, but significant, similarity to chalcone synthases and closely related enzymes (CHSRE) was also detected. The structure of the nschslk gene was found to be typical of the chalcone (chs)/stilbene (sts) synthase family. Expression of NSCHSLK mRNA was confined to microspores and tapetal cells. UV-irradiation or infection with Phytophthora parasitica var. nicotianae of transgenic Nicotiana benthamiana plants carrying a chimeric nschslk/GUS gene indicated that the nschslk promoter exhibits the same anther-specific, developmentally regulated expression pattern. Comparison of CHSRE and CHSLK polypeptide sequences revealed some important similarities and differences between the two groups. The data presented in this study, suggest that the anther-specific chslk genes represent a separate sub-family of plant polyketide synthases related to chs/sts in terms of gene structure, polypeptide sequence and the possible catalytic mechanism, but differing in substrate/product specificity. The putative role of CHSLK enzymes in anther development and particularly in exine synthesis is discussed.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">9869422</PMID><DateCompleted><Year>1999</Year><Month>01</Month><Day>15</Day></DateCompleted><DateRevised><Year>2019</Year><Month>08</Month><Day>22</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0167-4412</ISSN><JournalIssue CitedMedium="Print"><Volume>38</Volume><Issue>6</Issue><PubDate><Year>1998</Year><Month>Dec</Month></PubDate></JournalIssue><Title>Plant molecular biology</Title><ISOAbbreviation>Plant Mol Biol</ISOAbbreviation></Journal><ArticleTitle>Expression of an anther-specific chalcone synthase-like gene is correlated with uninucleate microspore development in Nicotiana sylvestris.</ArticleTitle><Pagination><MedlinePgn>1169-78</MedlinePgn></Pagination><Abstract><AbstractText>Two cDNA clones, specifically expressed in Nicotiana sylvestris anthers during uninucleate microspore development, were isolated using a subtractive hybridization approach. Sequence analysis showed that one of them, NSCHSLK, displayed a high level of similarity to several anther-specific chalcone synthase-like (CHSLK) proteins and an ORF from chromosome I of Arabidopsis thaliana. A lower, but significant, similarity to chalcone synthases and closely related enzymes (CHSRE) was also detected. The structure of the nschslk gene was found to be typical of the chalcone (chs)/stilbene (sts) synthase family. Expression of NSCHSLK mRNA was confined to microspores and tapetal cells. UV-irradiation or infection with Phytophthora parasitica var. nicotianae of transgenic Nicotiana benthamiana plants carrying a chimeric nschslk/GUS gene indicated that the nschslk promoter exhibits the same anther-specific, developmentally regulated expression pattern. Comparison of CHSRE and CHSLK polypeptide sequences revealed some important similarities and differences between the two groups. The data presented in this study, suggest that the anther-specific chslk genes represent a separate sub-family of plant polyketide synthases related to chs/sts in terms of gene structure, polypeptide sequence and the possible catalytic mechanism, but differing in substrate/product specificity. The putative role of CHSLK enzymes in anther development and particularly in exine synthesis is discussed.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Atanassov</LastName><ForeName>I</ForeName><Initials>I</Initials><AffiliationInfo><Affiliation>Institute of Genetic Engineering, Kostinbrod, Bulgaria. ivanatonassov@mailexcite.com</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Russinova</LastName><ForeName>E</ForeName><Initials>E</Initials></Author><Author ValidYN="Y"><LastName>Antonov</LastName><ForeName>L</ForeName><Initials>L</Initials></Author><Author ValidYN="Y"><LastName>Atanassov</LastName><ForeName>A</ForeName><Initials>A</Initials></Author></AuthorList><Language>eng</Language><DataBankList CompleteYN="Y"><DataBank><DataBankName>GENBANK</DataBankName><AccessionNumberList><AccessionNumber>Y14506</AccessionNumber><AccessionNumber>Y14507</AccessionNumber></AccessionNumberList></DataBank></DataBankList><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>Netherlands</Country><MedlineTA>Plant Mol Biol</MedlineTA><NlmUniqueID>9106343</NlmUniqueID><ISSNLinking>0167-4412</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D018076">DNA, Complementary</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D007527">Isoenzymes</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D011993">Recombinant Fusion Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 2.3.-</RegistryNumber><NameOfSubstance 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Molecular</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D015971" MajorTopicYN="N">Gene Expression Regulation, Enzymologic</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D018506" MajorTopicYN="Y">Gene Expression Regulation, Plant</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D007527" MajorTopicYN="N">Isoenzymes</DescriptorName><QualifierName UI="Q000096" MajorTopicYN="N">biosynthesis</QualifierName><QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008969" MajorTopicYN="N">Molecular Sequence Data</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D016366" MajorTopicYN="N">Open Reading Frames</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D010802" MajorTopicYN="N">Phylogeny</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D010947" MajorTopicYN="Y">Plants, Toxic</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D011993" MajorTopicYN="N">Recombinant Fusion Proteins</DescriptorName><QualifierName UI="Q000096" MajorTopicYN="N">biosynthesis</QualifierName><QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D016415" MajorTopicYN="N">Sequence Alignment</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D017386" MajorTopicYN="N">Sequence Homology, Amino Acid</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D013170" MajorTopicYN="N">Spores</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D014026" MajorTopicYN="N">Tobacco</DescriptorName><QualifierName UI="Q000201" MajorTopicYN="N">enzymology</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1998</Year><Month>12</Month><Day>30</Day></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>1998</Year><Month>12</Month><Day>30</Day><Hour>0</Hour><Minute>1</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>1998</Year><Month>12</Month><Day>30</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">9869422</ArticleId><ArticleId IdType="doi">10.1023/a:1006074508779</ArticleId></ArticleIdList><ReferenceList><Reference><Citation>Plant J. 1997 Jan;11(1):105-13</Citation><ArticleIdList><ArticleId IdType="pubmed">9025306</ArticleId></ArticleIdList></Reference><Reference><Citation>Plant Cell. 1993 Oct;5(10):1217-29</Citation><ArticleIdList><ArticleId IdType="pubmed">8281038</ArticleId></ArticleIdList></Reference><Reference><Citation>J Mol Evol. 1994 Jun;38(6):610-8</Citation><ArticleIdList><ArticleId 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Antonov</name><name sortKey="Atanassov, A" sort="Atanassov, A" uniqKey="Atanassov A" first="A" last="Atanassov">A. Atanassov</name><name sortKey="Russinova, E" sort="Russinova, E" uniqKey="Russinova E" first="E" last="Russinova">E. Russinova</name></noCountry><country name="Bulgarie"><noRegion><name sortKey="Atanassov, I" sort="Atanassov, I" uniqKey="Atanassov I" first="I" last="Atanassov">I. Atanassov</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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