The role of PopCel1 and PopCel2 in poplar leaf growth and cellulose biosynthesis.
Identifieur interne : 004373 ( Main/Exploration ); précédent : 004372; suivant : 004374The role of PopCel1 and PopCel2 in poplar leaf growth and cellulose biosynthesis.
Auteurs : Yasunori Ohmiya [Japon] ; Tomonori Nakai ; Yong Woo Park ; Takashi Aoyama ; Atsuhiro Oka ; Fukumi Sakai ; Takahisa HayashiSource :
- The Plant journal : for cell and molecular biology [ 0960-7412 ] ; 2003.
Descripteurs français
- KwdFr :
- ARN messager (génétique), ARN messager (métabolisme), Analyse de profil d'expression de gènes (MeSH), Cellulase (génétique), Cellulase (métabolisme), Cellulose (biosynthèse), Clonage moléculaire (MeSH), Données de séquences moléculaires (MeSH), Feuilles de plante (croissance et développement), Feuilles de plante (enzymologie), Feuilles de plante (génétique), Feuilles de plante (métabolisme), Gènes de plante (génétique), Induction enzymatique (effets des médicaments et des substances chimiques), Phylogenèse (MeSH), Populus (croissance et développement), Populus (enzymologie), Populus (génétique), Populus (métabolisme), Régulation de l'expression des gènes végétaux (effets des médicaments et des substances chimiques), Saccharose (métabolisme), Saccharose (pharmacologie), Végétaux génétiquement modifiés (MeSH), Éléments antisens (génétique) (génétique).
- MESH :
- biosynthèse : Cellulose.
- croissance et développement : Feuilles de plante, Populus.
- effets des médicaments et des substances chimiques : Induction enzymatique, Régulation de l'expression des gènes végétaux.
- enzymologie : Feuilles de plante, Populus.
- génétique : ARN messager, Cellulase, Feuilles de plante, Gènes de plante, Populus, Éléments antisens (génétique).
- métabolisme : ARN messager, Cellulase, Feuilles de plante, Populus, Saccharose.
- pharmacologie : Saccharose.
- Analyse de profil d'expression de gènes, Clonage moléculaire, Données de séquences moléculaires, Phylogenèse, Végétaux génétiquement modifiés.
English descriptors
- KwdEn :
- Antisense Elements (Genetics) (genetics), Cellulase (genetics), Cellulase (metabolism), Cellulose (biosynthesis), Cloning, Molecular (MeSH), Enzyme Induction (drug effects), Gene Expression Profiling (MeSH), Gene Expression Regulation, Plant (drug effects), Genes, Plant (genetics), Molecular Sequence Data (MeSH), Phylogeny (MeSH), Plant Leaves (enzymology), Plant Leaves (genetics), Plant Leaves (growth & development), Plant Leaves (metabolism), Plants, Genetically Modified (MeSH), Populus (enzymology), Populus (genetics), Populus (growth & development), Populus (metabolism), RNA, Messenger (genetics), RNA, Messenger (metabolism), Sucrose (metabolism), Sucrose (pharmacology).
- MESH :
- chemical , biosynthesis : Cellulose.
- chemical , genetics : Antisense Elements (Genetics), Cellulase, RNA, Messenger.
- chemical , metabolism : Cellulase, RNA, Messenger, Sucrose.
- drug effects : Enzyme Induction, Gene Expression Regulation, Plant.
- enzymology : Plant Leaves, Populus.
- genetics : Genes, Plant, Plant Leaves, Populus.
- growth & development : Plant Leaves, Populus.
- metabolism : Plant Leaves, Populus.
- chemical , pharmacology : Sucrose.
- Cloning, Molecular, Gene Expression Profiling, Molecular Sequence Data, Phylogeny, Plants, Genetically Modified.
Abstract
Poplar calli transcribed two cellulase (endo-1,4-beta-glucanase) genes, PopCel1 and PopCel2, whose mRNAs were differentially located in the growing leaves of poplar during cell wall synthesis. Histochemical and RT-PCR analyses of promoter-GUS fusion gene activities in transgenic poplar demonstrated that PopCel1 promoter-derived GUS activity was localized in the petiole and leaf veins, whereas PopCel2 was confined to mesophyll cells and disappeared from the tip during the development of leaves. Autoradiography of the leaf showed that the radioactivity of [14C]sucrose incorporated into cellulose corresponded to the combination of the sucrose-induced tissue-specific patterns of PopCel1 and PopCel2. Interestingly, 2,6-dichlorobenzonitrile (DCB) not only inhibited the incorporation of the radioactivity into cellulose, but also repressed the induction of both cellulase genes. Suppression of cellulases by expression of PopCel1 antisense cDNA or co-suppression of PopCel1 mRNA by overexpression of PopCel1 sense cDNA reduced leaf growth. Therefore, we came to the conclusion that PopCel1 and PopCel2 probably function to promote leaf growth in poplar by the endohydrolysis of 1,4-beta-glucan.
DOI: 10.1046/j.1365-313x.2003.01695.x
PubMed: 12631332
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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Messenger (metabolism)</term><term>Sucrose (metabolism)</term><term>Sucrose (pharmacology)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>ARN messager (génétique)</term><term>ARN messager (métabolisme)</term><term>Analyse de profil d'expression de gènes (MeSH)</term><term>Cellulase (génétique)</term><term>Cellulase (métabolisme)</term><term>Cellulose (biosynthèse)</term><term>Clonage moléculaire (MeSH)</term><term>Données de séquences moléculaires (MeSH)</term><term>Feuilles de plante (croissance et développement)</term><term>Feuilles de plante (enzymologie)</term><term>Feuilles de plante (génétique)</term><term>Feuilles de plante (métabolisme)</term><term>Gènes de plante (génétique)</term><term>Induction enzymatique (effets des médicaments et des substances chimiques)</term><term>Phylogenèse (MeSH)</term><term>Populus (croissance et développement)</term><term>Populus (enzymologie)</term><term>Populus (génétique)</term><term>Populus (métabolisme)</term><term>Régulation de l'expression des gènes végétaux (effets des médicaments et des substances chimiques)</term><term>Saccharose (métabolisme)</term><term>Saccharose (pharmacologie)</term><term>Végétaux génétiquement modifiés (MeSH)</term><term>Éléments antisens (génétique) (génétique)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="biosynthesis" xml:lang="en"><term>Cellulose</term></keywords><keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Antisense Elements (Genetics)</term><term>Cellulase</term><term>RNA, Messenger</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Cellulase</term><term>RNA, Messenger</term><term>Sucrose</term></keywords><keywords scheme="MESH" qualifier="biosynthèse" xml:lang="fr"><term>Cellulose</term></keywords><keywords scheme="MESH" qualifier="croissance et développement" xml:lang="fr"><term>Feuilles de plante</term><term>Populus</term></keywords><keywords scheme="MESH" 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moléculaires</term><term>Phylogenèse</term><term>Végétaux génétiquement modifiés</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Poplar calli transcribed two cellulase (endo-1,4-beta-glucanase) genes, PopCel1 and PopCel2, whose mRNAs were differentially located in the growing leaves of poplar during cell wall synthesis. Histochemical and RT-PCR analyses of promoter-GUS fusion gene activities in transgenic poplar demonstrated that PopCel1 promoter-derived GUS activity was localized in the petiole and leaf veins, whereas PopCel2 was confined to mesophyll cells and disappeared from the tip during the development of leaves. Autoradiography of the leaf showed that the radioactivity of [14C]sucrose incorporated into cellulose corresponded to the combination of the sucrose-induced tissue-specific patterns of PopCel1 and PopCel2. Interestingly, 2,6-dichlorobenzonitrile (DCB) not only inhibited the incorporation of the radioactivity into cellulose, but also repressed the induction of both cellulase genes. Suppression of cellulases by expression of PopCel1 antisense cDNA or co-suppression of PopCel1 mRNA by overexpression of PopCel1 sense cDNA reduced leaf growth. Therefore, we came to the conclusion that PopCel1 and PopCel2 probably function to promote leaf growth in poplar by the endohydrolysis of 1,4-beta-glucan.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">12631332</PMID><DateCompleted><Year>2003</Year><Month>12</Month><Day>10</Day></DateCompleted><DateRevised><Year>2019</Year><Month>09</Month><Day>06</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0960-7412</ISSN><JournalIssue CitedMedium="Print"><Volume>33</Volume><Issue>6</Issue><PubDate><Year>2003</Year><Month>Mar</Month></PubDate></JournalIssue><Title>The Plant journal : for cell and molecular biology</Title><ISOAbbreviation>Plant J</ISOAbbreviation></Journal><ArticleTitle>The role of PopCel1 and PopCel2 in poplar leaf growth and cellulose biosynthesis.</ArticleTitle><Pagination><MedlinePgn>1087-97</MedlinePgn></Pagination><Abstract><AbstractText>Poplar calli transcribed two cellulase (endo-1,4-beta-glucanase) genes, PopCel1 and PopCel2, whose mRNAs were differentially located in the growing leaves of poplar during cell wall synthesis. Histochemical and RT-PCR analyses of promoter-GUS fusion gene activities in transgenic poplar demonstrated that PopCel1 promoter-derived GUS activity was localized in the petiole and leaf veins, whereas PopCel2 was confined to mesophyll cells and disappeared from the tip during the development of leaves. Autoradiography of the leaf showed that the radioactivity of [14C]sucrose incorporated into cellulose corresponded to the combination of the sucrose-induced tissue-specific patterns of PopCel1 and PopCel2. Interestingly, 2,6-dichlorobenzonitrile (DCB) not only inhibited the incorporation of the radioactivity into cellulose, but also repressed the induction of both cellulase genes. Suppression of cellulases by expression of PopCel1 antisense cDNA or co-suppression of PopCel1 mRNA by overexpression of PopCel1 sense cDNA reduced leaf growth. Therefore, we came to the conclusion that PopCel1 and PopCel2 probably function to promote leaf growth in poplar by the endohydrolysis of 1,4-beta-glucan.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Ohmiya</LastName><ForeName>Yasunori</ForeName><Initials>Y</Initials><AffiliationInfo><Affiliation>Wood Research Institute, Kyoto University, Uji, Kyoto 611-0011, Japan.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Nakai</LastName><ForeName>Tomonori</ForeName><Initials>T</Initials></Author><Author ValidYN="Y"><LastName>Park</LastName><ForeName>Yong Woo</ForeName><Initials>YW</Initials></Author><Author ValidYN="Y"><LastName>Aoyama</LastName><ForeName>Takashi</ForeName><Initials>T</Initials></Author><Author ValidYN="Y"><LastName>Oka</LastName><ForeName>Atsuhiro</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Sakai</LastName><ForeName>Fukumi</ForeName><Initials>F</Initials></Author><Author ValidYN="Y"><LastName>Hayashi</LastName><ForeName>Takahisa</ForeName><Initials>T</Initials></Author></AuthorList><Language>eng</Language><DataBankList 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UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>Plant J</MedlineTA><NlmUniqueID>9207397</NlmUniqueID><ISSNLinking>0960-7412</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D016375">Antisense Elements (Genetics)</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D012333">RNA, Messenger</NameOfSubstance></Chemical><Chemical><RegistryNumber>57-50-1</RegistryNumber><NameOfSubstance UI="D013395">Sucrose</NameOfSubstance></Chemical><Chemical><RegistryNumber>9004-34-6</RegistryNumber><NameOfSubstance UI="D002482">Cellulose</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 3.2.1.4</RegistryNumber><NameOfSubstance UI="D002480">Cellulase</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D016375" MajorTopicYN="N">Antisense Elements (Genetics)</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002480" MajorTopicYN="N">Cellulase</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002482" MajorTopicYN="N">Cellulose</DescriptorName><QualifierName UI="Q000096" MajorTopicYN="Y">biosynthesis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003001" MajorTopicYN="N">Cloning, Molecular</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D004790" MajorTopicYN="N">Enzyme Induction</DescriptorName><QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D020869" MajorTopicYN="N">Gene Expression Profiling</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D018506" MajorTopicYN="N">Gene Expression Regulation, Plant</DescriptorName><QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D017343" MajorTopicYN="N">Genes, Plant</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008969" MajorTopicYN="N">Molecular Sequence Data</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D010802" MajorTopicYN="N">Phylogeny</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D018515" MajorTopicYN="N">Plant Leaves</DescriptorName><QualifierName UI="Q000201" MajorTopicYN="N">enzymology</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000254" MajorTopicYN="Y">growth & development</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D030821" MajorTopicYN="N">Plants, Genetically Modified</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D032107" MajorTopicYN="N">Populus</DescriptorName><QualifierName UI="Q000201" MajorTopicYN="N">enzymology</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000254" MajorTopicYN="Y">growth & development</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012333" MajorTopicYN="N">RNA, Messenger</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013395" MajorTopicYN="N">Sucrose</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName><QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2003</Year><Month>3</Month><Day>13</Day><Hour>4</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2003</Year><Month>12</Month><Day>12</Day><Hour>5</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2003</Year><Month>3</Month><Day>13</Day><Hour>4</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">12631332</ArticleId><ArticleId IdType="pii">1695</ArticleId><ArticleId IdType="doi">10.1046/j.1365-313x.2003.01695.x</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Japon</li></country><region><li>Région du Kansai</li></region><settlement><li>Kyoto</li></settlement><orgName><li>Université de Kyoto</li></orgName></list><tree><noCountry><name sortKey="Aoyama, Takashi" sort="Aoyama, Takashi" uniqKey="Aoyama T" first="Takashi" last="Aoyama">Takashi Aoyama</name><name sortKey="Hayashi, Takahisa" sort="Hayashi, Takahisa" uniqKey="Hayashi T" first="Takahisa" last="Hayashi">Takahisa Hayashi</name><name sortKey="Nakai, Tomonori" sort="Nakai, Tomonori" uniqKey="Nakai T" first="Tomonori" last="Nakai">Tomonori Nakai</name><name sortKey="Oka, Atsuhiro" sort="Oka, Atsuhiro" uniqKey="Oka A" first="Atsuhiro" last="Oka">Atsuhiro Oka</name><name sortKey="Park, Yong Woo" sort="Park, Yong Woo" uniqKey="Park Y" first="Yong Woo" last="Park">Yong Woo Park</name><name sortKey="Sakai, Fukumi" sort="Sakai, Fukumi" uniqKey="Sakai F" first="Fukumi" last="Sakai">Fukumi Sakai</name></noCountry><country name="Japon"><region name="Région du Kansai"><name sortKey="Ohmiya, Yasunori" sort="Ohmiya, Yasunori" uniqKey="Ohmiya Y" first="Yasunori" last="Ohmiya">Yasunori Ohmiya</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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