cDNA cloning of six mRNAs induced by TMV infection of tobacco and a characterization of their translation products.
Identifieur interne : 000560 ( Main/Curation ); précédent : 000559; suivant : 000561cDNA cloning of six mRNAs induced by TMV infection of tobacco and a characterization of their translation products.
Auteurs : R A Hooft Van Huijsduijnen [Pays-Bas] ; L C Van Loon ; J F BolSource :
- The EMBO journal [ 0261-4189 ] ; 1986.
Descripteurs français
- KwdFr :
- ADN complémentaire (génétique), ARN des plantes (génétique), ARN messager (génétique), Biosynthèse des protéines (MeSH), Clonage moléculaire (MeSH), Hybridation d'acides nucléiques (MeSH), Protéines végétales (génétique), Tabac (virologie), Technique de Northern (MeSH), Virus de la mosaïque du tabac (génétique).
- MESH :
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : DNA, Complementary, Plant Proteins, RNA, Messenger, RNA, Plant.
- genetics : Tobacco Mosaic Virus.
- virology : Tobacco.
- Blotting, Northern, Cloning, Molecular, Nucleic Acid Hybridization, Protein Biosynthesis.
Abstract
A cDNA library was constructed to 10-15 S poly(A) RNA from tobacco mosaic virus (MV)-infected Samsun NN tobacco.By differential colony hybridization of 1400 transformants,32 clones were obtained corresponding to TMV-inducible tobacco mRNAs. These clones were subdivided into six clusters on the basis of cross-hybridization of the inserts. By Northern blot hybridization it was shown that three of the corresponding mRNAs were strongly induced by spraying tobacco plants with salicylic acid, whereas one mRNA was weakly induced by this treatment. All mRNAs were systemically induced in plants in which only the lower leaves were locally infected by TMV. Hybrid-selected translation was performed, using six clones representing one cluster each, followed by immunoprecipitation using an antiserum to purified pathogenesis-related (PR) proteins. Four clones yielded precipitable translation products. One of these clones represented a cluster of PR-1 clones, another clone encoded the thaumatin-like (TL) protein of tobacco which may correspond to PR-P or -Q.
PubMed: 16453701
PubMed Central: PMC1167082
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pubmed:16453701Le document en format XML
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<affiliation wicri:level="1"><nlm:affiliation>Department of Biochemistry, State University of Leiden, Wassenaarseweg 64, 2333 AL Leiden, and Department of Plant Physiology, Agricultural University, Arboretumlaan 4, 6703 BD Wageningen, The Netherlands.</nlm:affiliation>
<country xml:lang="fr">Pays-Bas</country>
<wicri:regionArea>Department of Biochemistry, State University of Leiden, Wassenaarseweg 64, 2333 AL Leiden, and Department of Plant Physiology, Agricultural University, Arboretumlaan 4, 6703 BD Wageningen</wicri:regionArea>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">cDNA cloning of six mRNAs induced by TMV infection of tobacco and a characterization of their translation products.</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Blotting, Northern (MeSH)</term>
<term>Cloning, Molecular (MeSH)</term>
<term>DNA, Complementary (genetics)</term>
<term>Nucleic Acid Hybridization (MeSH)</term>
<term>Plant Proteins (genetics)</term>
<term>Protein Biosynthesis (MeSH)</term>
<term>RNA, Messenger (genetics)</term>
<term>RNA, Plant (genetics)</term>
<term>Tobacco (virology)</term>
<term>Tobacco Mosaic Virus (genetics)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>ADN complémentaire (génétique)</term>
<term>ARN des plantes (génétique)</term>
<term>ARN messager (génétique)</term>
<term>Biosynthèse des protéines (MeSH)</term>
<term>Clonage moléculaire (MeSH)</term>
<term>Hybridation d'acides nucléiques (MeSH)</term>
<term>Protéines végétales (génétique)</term>
<term>Tabac (virologie)</term>
<term>Technique de Northern (MeSH)</term>
<term>Virus de la mosaïque du tabac (génétique)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>DNA, Complementary</term>
<term>Plant Proteins</term>
<term>RNA, Messenger</term>
<term>RNA, Plant</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Tobacco Mosaic Virus</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>ADN complémentaire</term>
<term>ARN des plantes</term>
<term>ARN messager</term>
<term>Protéines végétales</term>
<term>Virus de la mosaïque du tabac</term>
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<keywords scheme="MESH" qualifier="virologie" xml:lang="fr"><term>Tabac</term>
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<keywords scheme="MESH" qualifier="virology" xml:lang="en"><term>Tobacco</term>
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<term>Cloning, Molecular</term>
<term>Nucleic Acid Hybridization</term>
<term>Protein Biosynthesis</term>
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<keywords scheme="MESH" xml:lang="fr"><term>Biosynthèse des protéines</term>
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<term>Hybridation d'acides nucléiques</term>
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<front><div type="abstract" xml:lang="en">A cDNA library was constructed to 10-15 S poly(A) RNA from tobacco mosaic virus (MV)-infected Samsun NN tobacco.By differential colony hybridization of 1400 transformants,32 clones were obtained corresponding to TMV-inducible tobacco mRNAs. These clones were subdivided into six clusters on the basis of cross-hybridization of the inserts. By Northern blot hybridization it was shown that three of the corresponding mRNAs were strongly induced by spraying tobacco plants with salicylic acid, whereas one mRNA was weakly induced by this treatment. All mRNAs were systemically induced in plants in which only the lower leaves were locally infected by TMV. Hybrid-selected translation was performed, using six clones representing one cluster each, followed by immunoprecipitation using an antiserum to purified pathogenesis-related (PR) proteins. Four clones yielded precipitable translation products. One of these clones represented a cluster of PR-1 clones, another clone encoded the thaumatin-like (TL) protein of tobacco which may correspond to PR-P or -Q.</div>
</front>
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<ArticleTitle>cDNA cloning of six mRNAs induced by TMV infection of tobacco and a characterization of their translation products.</ArticleTitle>
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<Abstract><AbstractText>A cDNA library was constructed to 10-15 S poly(A) RNA from tobacco mosaic virus (MV)-infected Samsun NN tobacco.By differential colony hybridization of 1400 transformants,32 clones were obtained corresponding to TMV-inducible tobacco mRNAs. These clones were subdivided into six clusters on the basis of cross-hybridization of the inserts. By Northern blot hybridization it was shown that three of the corresponding mRNAs were strongly induced by spraying tobacco plants with salicylic acid, whereas one mRNA was weakly induced by this treatment. All mRNAs were systemically induced in plants in which only the lower leaves were locally infected by TMV. Hybrid-selected translation was performed, using six clones representing one cluster each, followed by immunoprecipitation using an antiserum to purified pathogenesis-related (PR) proteins. Four clones yielded precipitable translation products. One of these clones represented a cluster of PR-1 clones, another clone encoded the thaumatin-like (TL) protein of tobacco which may correspond to PR-P or -Q.</AbstractText>
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