Gene activation by UV light, fungal elicitor or fungal infection in Petroselinum crispum is correlated with repression of cell cycle-related genes.
Identifieur interne : 002B80 ( Main/Exploration ); précédent : 002B79; suivant : 002B81Gene activation by UV light, fungal elicitor or fungal infection in Petroselinum crispum is correlated with repression of cell cycle-related genes.
Auteurs : E. Logemann [Allemagne] ; S C Wu ; J. Schröder ; E. Schmelzer ; I E Somssich ; K. HahlbrockSource :
- The Plant journal : for cell and molecular biology [ 0960-7412 ] ; 1995.
Descripteurs français
- KwdFr :
- ARN messager (analyse), ARN messager (biosynthèse), Activation de la transcription (MeSH), Cellules cultivées (MeSH), Cinétique (MeSH), Cycle cellulaire (génétique), Cyclines (biosynthèse), Cyclines (génétique), Division cellulaire (MeSH), Données de séquences moléculaires (MeSH), Famille multigénique (MeSH), Flavonoïdes (biosynthèse), Fragments peptidiques (métabolisme), Glycoprotéines membranaires (métabolisme), Gènes de plante (effets des radiations), Histone (biosynthèse), Histone (génétique), Induction enzymatique (MeSH), Magnoliopsida (effets des radiations), Magnoliopsida (génétique), Magnoliopsida (microbiologie), Phenylalanine ammonia-lyase (biosynthèse), Phytophthora (pathogénicité), Phytophthora (physiologie), Protéine-kinase CDC2 (biosynthèse), Protéine-kinase CDC2 (génétique), Protéines fongiques (métabolisme), Rayons ultraviolets (MeSH), Régulation de l'expression des gènes végétaux (effets des radiations), Répression enzymatique (MeSH), Séquence d'acides aminés (MeSH), Séquence nucléotidique (MeSH), Transcription génétique (MeSH).
- MESH :
- analyse : ARN messager.
- biosynthèse : ARN messager, Cyclines, Flavonoïdes, Histone, Phenylalanine ammonia-lyase, Protéine-kinase CDC2.
- effets des radiations : Gènes de plante, Magnoliopsida, Régulation de l'expression des gènes végétaux.
- génétique : Cycle cellulaire, Cyclines, Histone, Magnoliopsida, Protéine-kinase CDC2.
- microbiologie : Magnoliopsida.
- métabolisme : Fragments peptidiques, Glycoprotéines membranaires, Protéines fongiques.
- pathogénicité : Phytophthora.
- physiologie : Phytophthora.
- Activation de la transcription, Cellules cultivées, Cinétique, Division cellulaire, Données de séquences moléculaires, Famille multigénique, Induction enzymatique, Rayons ultraviolets, Répression enzymatique, Séquence d'acides aminés, Séquence nucléotidique, Transcription génétique.
English descriptors
- KwdEn :
- Amino Acid Sequence (MeSH), Base Sequence (MeSH), CDC2 Protein Kinase (biosynthesis), CDC2 Protein Kinase (genetics), Cell Cycle (genetics), Cell Division (MeSH), Cells, Cultured (MeSH), Cyclins (biosynthesis), Cyclins (genetics), Enzyme Induction (MeSH), Enzyme Repression (MeSH), Flavonoids (biosynthesis), Fungal Proteins (metabolism), Gene Expression Regulation, Plant (radiation effects), Genes, Plant (radiation effects), Histones (biosynthesis), Histones (genetics), Kinetics (MeSH), Magnoliopsida (genetics), Magnoliopsida (microbiology), Magnoliopsida (radiation effects), Membrane Glycoproteins (metabolism), Molecular Sequence Data (MeSH), Multigene Family (MeSH), Peptide Fragments (metabolism), Phenylalanine Ammonia-Lyase (biosynthesis), Phytophthora (pathogenicity), Phytophthora (physiology), RNA, Messenger (analysis), RNA, Messenger (biosynthesis), Transcription, Genetic (MeSH), Transcriptional Activation (MeSH), Ultraviolet Rays (MeSH).
- MESH :
- chemical , analysis : RNA, Messenger.
- chemical , biosynthesis : CDC2 Protein Kinase, Cyclins, Flavonoids, Histones, Phenylalanine Ammonia-Lyase, RNA, Messenger.
- chemical , genetics : CDC2 Protein Kinase, Cyclins, Histones.
- genetics : Cell Cycle, Magnoliopsida.
- chemical , metabolism : Fungal Proteins, Membrane Glycoproteins, Peptide Fragments.
- microbiology : Magnoliopsida.
- pathogenicity : Phytophthora.
- physiology : Phytophthora.
- radiation effects : Gene Expression Regulation, Plant, Genes, Plant, Magnoliopsida.
- Amino Acid Sequence, Base Sequence, Cell Division, Cells, Cultured, Enzyme Induction, Enzyme Repression, Kinetics, Molecular Sequence Data, Multigene Family, Transcription, Genetic, Transcriptional Activation, Ultraviolet Rays.
Abstract
The effects of UV light or fungal elicitors on plant cells have so far been studied mostly with respect to defense-related gene activation. Here, an inverse correlation of these stimulatory effects with the activities of several cell cycle-related genes is demonstrated. Concomitant with the induction of flavonoid biosynthetic enzymes in UV-irradiated cell suspension cultures of parsley (Petroselinum crispum), total histone synthesis declined to about half the initial rate. A subclass of the histone H3 gene family was selected to demonstrate the close correlation of its expression with cell division, both in intact plants and cultured cells. Using RNA-blot and run-on transcription assays, it was shown that one arbitrarily selected subclass of each of the histone H2A, H2B, H3 and H4 gene families and of the genes encoding a p34cdc2 protein kinase and a mitotic cyclin were transcriptionally repressed in UV-irradiated as well as fungal elicitor-treated parsley cells. The timing and extent of repression differed between the two stimuli; the response to light was more transient and smaller in magnitude. These differential responses to light and elicitor were inversely correlated with the induction of phenylalanine ammonia-lyase, a key enzyme of phenylpropanoid metabolism. Essentially the same result was obtained with a defined oligopeptide elicitor, indicating that the same signaling pathway is responsible for defense-related gene activation and cell cycle-related gene repression. A temporary (UV light) or long-lasting (fungal elicitor) cessation of cell culture growth is most likely due to an arrest of cell division which may be a prerequisite for full commitment of the cells to transcriptional activation of full commitment of the cells to transcriptional activation of pathways involved in UV protection or pathogen defense. This conclusion is corroborated by the observation that the histone H3 mRNA level greatly declined around fungal infection sites in young parsley leaves.
DOI: 10.1046/j.1365-313x.1995.8060865.x
PubMed: 8580959
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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Logemann</name><affiliation wicri:level="3"><nlm:affiliation>Max-Planck-Institut für Züchtungsforschung, Abteilung Biochemie, Köln, Germany.</nlm:affiliation><country xml:lang="fr">Allemagne</country><wicri:regionArea>Max-Planck-Institut für Züchtungsforschung, Abteilung Biochemie, Köln</wicri:regionArea><placeName><region type="land" nuts="1">Rhénanie-du-Nord-Westphalie</region><region type="district" nuts="2">District de Cologne</region><settlement type="city">Cologne</settlement></placeName></affiliation></author><author><name sortKey="Wu, S C" sort="Wu, S C" uniqKey="Wu S" first="S C" last="Wu">S C Wu</name></author><author><name sortKey="Schroder, J" sort="Schroder, J" uniqKey="Schroder J" first="J" last="Schröder">J. Schröder</name></author><author><name sortKey="Schmelzer, E" sort="Schmelzer, E" uniqKey="Schmelzer E" first="E" last="Schmelzer">E. Schmelzer</name></author><author><name sortKey="Somssich, I E" sort="Somssich, I E" uniqKey="Somssich I" first="I E" last="Somssich">I E Somssich</name></author><author><name sortKey="Hahlbrock, K" sort="Hahlbrock, K" uniqKey="Hahlbrock K" first="K" last="Hahlbrock">K. Hahlbrock</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="1995">1995</date><idno type="RBID">pubmed:8580959</idno><idno type="pmid">8580959</idno><idno type="doi">10.1046/j.1365-313x.1995.8060865.x</idno><idno type="wicri:Area/Main/Corpus">002B55</idno><idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Corpus" wicri:corpus="PubMed">002B55</idno><idno type="wicri:Area/Main/Curation">002B55</idno><idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Curation">002B55</idno><idno type="wicri:Area/Main/Exploration">002B55</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Gene activation by UV light, fungal elicitor or fungal infection in Petroselinum crispum is correlated with repression of cell cycle-related genes.</title><author><name sortKey="Logemann, E" sort="Logemann, E" uniqKey="Logemann E" first="E" last="Logemann">E. Logemann</name><affiliation wicri:level="3"><nlm:affiliation>Max-Planck-Institut für Züchtungsforschung, Abteilung Biochemie, Köln, Germany.</nlm:affiliation><country xml:lang="fr">Allemagne</country><wicri:regionArea>Max-Planck-Institut für Züchtungsforschung, Abteilung Biochemie, Köln</wicri:regionArea><placeName><region type="land" nuts="1">Rhénanie-du-Nord-Westphalie</region><region type="district" nuts="2">District de Cologne</region><settlement type="city">Cologne</settlement></placeName></affiliation></author><author><name sortKey="Wu, S C" sort="Wu, S C" uniqKey="Wu S" first="S C" last="Wu">S C Wu</name></author><author><name sortKey="Schroder, J" sort="Schroder, J" uniqKey="Schroder J" first="J" last="Schröder">J. Schröder</name></author><author><name sortKey="Schmelzer, E" sort="Schmelzer, E" uniqKey="Schmelzer E" first="E" last="Schmelzer">E. Schmelzer</name></author><author><name sortKey="Somssich, I E" sort="Somssich, I E" uniqKey="Somssich I" first="I E" last="Somssich">I E Somssich</name></author><author><name sortKey="Hahlbrock, K" sort="Hahlbrock, K" uniqKey="Hahlbrock K" first="K" last="Hahlbrock">K. Hahlbrock</name></author></analytic><series><title level="j">The Plant journal : for cell and molecular biology</title><idno type="ISSN">0960-7412</idno><imprint><date when="1995" type="published">1995</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Amino Acid Sequence (MeSH)</term><term>Base Sequence (MeSH)</term><term>CDC2 Protein Kinase (biosynthesis)</term><term>CDC2 Protein Kinase (genetics)</term><term>Cell Cycle (genetics)</term><term>Cell Division (MeSH)</term><term>Cells, Cultured (MeSH)</term><term>Cyclins (biosynthesis)</term><term>Cyclins (genetics)</term><term>Enzyme Induction (MeSH)</term><term>Enzyme Repression (MeSH)</term><term>Flavonoids (biosynthesis)</term><term>Fungal Proteins (metabolism)</term><term>Gene Expression Regulation, Plant (radiation effects)</term><term>Genes, Plant (radiation effects)</term><term>Histones (biosynthesis)</term><term>Histones (genetics)</term><term>Kinetics (MeSH)</term><term>Magnoliopsida (genetics)</term><term>Magnoliopsida (microbiology)</term><term>Magnoliopsida (radiation effects)</term><term>Membrane Glycoproteins (metabolism)</term><term>Molecular Sequence Data (MeSH)</term><term>Multigene Family (MeSH)</term><term>Peptide Fragments (metabolism)</term><term>Phenylalanine Ammonia-Lyase (biosynthesis)</term><term>Phytophthora (pathogenicity)</term><term>Phytophthora (physiology)</term><term>RNA, Messenger (analysis)</term><term>RNA, Messenger (biosynthesis)</term><term>Transcription, Genetic (MeSH)</term><term>Transcriptional Activation (MeSH)</term><term>Ultraviolet Rays (MeSH)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>ARN messager (analyse)</term><term>ARN messager (biosynthèse)</term><term>Activation de la transcription (MeSH)</term><term>Cellules cultivées (MeSH)</term><term>Cinétique (MeSH)</term><term>Cycle cellulaire (génétique)</term><term>Cyclines (biosynthèse)</term><term>Cyclines (génétique)</term><term>Division cellulaire (MeSH)</term><term>Données de séquences moléculaires (MeSH)</term><term>Famille multigénique (MeSH)</term><term>Flavonoïdes (biosynthèse)</term><term>Fragments peptidiques (métabolisme)</term><term>Glycoprotéines membranaires (métabolisme)</term><term>Gènes de plante (effets des radiations)</term><term>Histone (biosynthèse)</term><term>Histone (génétique)</term><term>Induction enzymatique (MeSH)</term><term>Magnoliopsida (effets des radiations)</term><term>Magnoliopsida (génétique)</term><term>Magnoliopsida (microbiologie)</term><term>Phenylalanine ammonia-lyase (biosynthèse)</term><term>Phytophthora (pathogénicité)</term><term>Phytophthora (physiologie)</term><term>Protéine-kinase CDC2 (biosynthèse)</term><term>Protéine-kinase CDC2 (génétique)</term><term>Protéines fongiques (métabolisme)</term><term>Rayons ultraviolets (MeSH)</term><term>Régulation de l'expression des gènes végétaux (effets des radiations)</term><term>Répression enzymatique (MeSH)</term><term>Séquence d'acides aminés (MeSH)</term><term>Séquence nucléotidique (MeSH)</term><term>Transcription génétique (MeSH)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en"><term>RNA, Messenger</term></keywords><keywords scheme="MESH" type="chemical" qualifier="biosynthesis" xml:lang="en"><term>CDC2 Protein Kinase</term><term>Cyclins</term><term>Flavonoids</term><term>Histones</term><term>Phenylalanine Ammonia-Lyase</term><term>RNA, Messenger</term></keywords><keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>CDC2 Protein Kinase</term><term>Cyclins</term><term>Histones</term></keywords><keywords scheme="MESH" qualifier="analyse" xml:lang="fr"><term>ARN messager</term></keywords><keywords scheme="MESH" qualifier="biosynthèse" xml:lang="fr"><term>ARN messager</term><term>Cyclines</term><term>Flavonoïdes</term><term>Histone</term><term>Phenylalanine ammonia-lyase</term><term>Protéine-kinase CDC2</term></keywords><keywords scheme="MESH" qualifier="effets des radiations" xml:lang="fr"><term>Gènes de plante</term><term>Magnoliopsida</term><term>Régulation de l'expression des gènes végétaux</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Cell Cycle</term><term>Magnoliopsida</term></keywords><keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Cycle cellulaire</term><term>Cyclines</term><term>Histone</term><term>Magnoliopsida</term><term>Protéine-kinase CDC2</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Fungal Proteins</term><term>Membrane Glycoproteins</term><term>Peptide Fragments</term></keywords><keywords scheme="MESH" qualifier="microbiologie" xml:lang="fr"><term>Magnoliopsida</term></keywords><keywords scheme="MESH" qualifier="microbiology" xml:lang="en"><term>Magnoliopsida</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Fragments peptidiques</term><term>Glycoprotéines membranaires</term><term>Protéines fongiques</term></keywords><keywords scheme="MESH" qualifier="pathogenicity" xml:lang="en"><term>Phytophthora</term></keywords><keywords scheme="MESH" qualifier="pathogénicité" xml:lang="fr"><term>Phytophthora</term></keywords><keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Phytophthora</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Phytophthora</term></keywords><keywords scheme="MESH" qualifier="radiation effects" xml:lang="en"><term>Gene Expression Regulation, Plant</term><term>Genes, Plant</term><term>Magnoliopsida</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Amino Acid Sequence</term><term>Base Sequence</term><term>Cell Division</term><term>Cells, Cultured</term><term>Enzyme Induction</term><term>Enzyme Repression</term><term>Kinetics</term><term>Molecular Sequence Data</term><term>Multigene Family</term><term>Transcription, Genetic</term><term>Transcriptional Activation</term><term>Ultraviolet Rays</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Activation de la transcription</term><term>Cellules cultivées</term><term>Cinétique</term><term>Division cellulaire</term><term>Données de séquences moléculaires</term><term>Famille multigénique</term><term>Induction enzymatique</term><term>Rayons ultraviolets</term><term>Répression enzymatique</term><term>Séquence d'acides aminés</term><term>Séquence nucléotidique</term><term>Transcription génétique</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The effects of UV light or fungal elicitors on plant cells have so far been studied mostly with respect to defense-related gene activation. Here, an inverse correlation of these stimulatory effects with the activities of several cell cycle-related genes is demonstrated. Concomitant with the induction of flavonoid biosynthetic enzymes in UV-irradiated cell suspension cultures of parsley (Petroselinum crispum), total histone synthesis declined to about half the initial rate. A subclass of the histone H3 gene family was selected to demonstrate the close correlation of its expression with cell division, both in intact plants and cultured cells. Using RNA-blot and run-on transcription assays, it was shown that one arbitrarily selected subclass of each of the histone H2A, H2B, H3 and H4 gene families and of the genes encoding a p34cdc2 protein kinase and a mitotic cyclin were transcriptionally repressed in UV-irradiated as well as fungal elicitor-treated parsley cells. The timing and extent of repression differed between the two stimuli; the response to light was more transient and smaller in magnitude. These differential responses to light and elicitor were inversely correlated with the induction of phenylalanine ammonia-lyase, a key enzyme of phenylpropanoid metabolism. Essentially the same result was obtained with a defined oligopeptide elicitor, indicating that the same signaling pathway is responsible for defense-related gene activation and cell cycle-related gene repression. A temporary (UV light) or long-lasting (fungal elicitor) cessation of cell culture growth is most likely due to an arrest of cell division which may be a prerequisite for full commitment of the cells to transcriptional activation of full commitment of the cells to transcriptional activation of pathways involved in UV protection or pathogen defense. This conclusion is corroborated by the observation that the histone H3 mRNA level greatly declined around fungal infection sites in young parsley leaves.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">8580959</PMID><DateCompleted><Year>1996</Year><Month>03</Month><Day>19</Day></DateCompleted><DateRevised><Year>2019</Year><Month>09</Month><Day>05</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0960-7412</ISSN><JournalIssue CitedMedium="Print"><Volume>8</Volume><Issue>6</Issue><PubDate><Year>1995</Year><Month>Dec</Month></PubDate></JournalIssue><Title>The Plant journal : for cell and molecular biology</Title><ISOAbbreviation>Plant J</ISOAbbreviation></Journal><ArticleTitle>Gene activation by UV light, fungal elicitor or fungal infection in Petroselinum crispum is correlated with repression of cell cycle-related genes.</ArticleTitle><Pagination><MedlinePgn>865-76</MedlinePgn></Pagination><Abstract><AbstractText>The effects of UV light or fungal elicitors on plant cells have so far been studied mostly with respect to defense-related gene activation. Here, an inverse correlation of these stimulatory effects with the activities of several cell cycle-related genes is demonstrated. Concomitant with the induction of flavonoid biosynthetic enzymes in UV-irradiated cell suspension cultures of parsley (Petroselinum crispum), total histone synthesis declined to about half the initial rate. A subclass of the histone H3 gene family was selected to demonstrate the close correlation of its expression with cell division, both in intact plants and cultured cells. Using RNA-blot and run-on transcription assays, it was shown that one arbitrarily selected subclass of each of the histone H2A, H2B, H3 and H4 gene families and of the genes encoding a p34cdc2 protein kinase and a mitotic cyclin were transcriptionally repressed in UV-irradiated as well as fungal elicitor-treated parsley cells. The timing and extent of repression differed between the two stimuli; the response to light was more transient and smaller in magnitude. These differential responses to light and elicitor were inversely correlated with the induction of phenylalanine ammonia-lyase, a key enzyme of phenylpropanoid metabolism. Essentially the same result was obtained with a defined oligopeptide elicitor, indicating that the same signaling pathway is responsible for defense-related gene activation and cell cycle-related gene repression. A temporary (UV light) or long-lasting (fungal elicitor) cessation of cell culture growth is most likely due to an arrest of cell division which may be a prerequisite for full commitment of the cells to transcriptional activation of full commitment of the cells to transcriptional activation of pathways involved in UV protection or pathogen defense. This conclusion is corroborated by the observation that the histone H3 mRNA level greatly declined around fungal infection sites in young parsley leaves.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Logemann</LastName><ForeName>E</ForeName><Initials>E</Initials><AffiliationInfo><Affiliation>Max-Planck-Institut für Züchtungsforschung, Abteilung Biochemie, Köln, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Wu</LastName><ForeName>S C</ForeName><Initials>SC</Initials></Author><Author ValidYN="Y"><LastName>Schröder</LastName><ForeName>J</ForeName><Initials>J</Initials></Author><Author ValidYN="Y"><LastName>Schmelzer</LastName><ForeName>E</ForeName><Initials>E</Initials></Author><Author ValidYN="Y"><LastName>Somssich</LastName><ForeName>I E</ForeName><Initials>IE</Initials></Author><Author ValidYN="Y"><LastName>Hahlbrock</LastName><ForeName>K</ForeName><Initials>K</Initials></Author></AuthorList><Language>eng</Language><DataBankList CompleteYN="Y"><DataBank><DataBankName>GENBANK</DataBankName><AccessionNumberList><AccessionNumber>L34206</AccessionNumber><AccessionNumber>L34207</AccessionNumber></AccessionNumberList></DataBank></DataBankList><PublicationTypeList><PublicationType UI="D003160">Comparative Study</PublicationType><PublicationType 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="D016213">Cyclins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D005419">Flavonoids</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D005656">Fungal Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D006657">Histones</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D008562">Membrane Glycoproteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D010446">Peptide Fragments</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D012333">RNA, Messenger</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="C091510">elicitor protein, Phytophthora megasperma</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 2.7.11.22</RegistryNumber><NameOfSubstance UI="D016203">CDC2 Protein Kinase</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 4.3.1.24</RegistryNumber><NameOfSubstance UI="D010650">Phenylalanine Ammonia-Lyase</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000595" MajorTopicYN="N">Amino Acid Sequence</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D001483" MajorTopicYN="N">Base Sequence</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D016203" MajorTopicYN="N">CDC2 Protein Kinase</DescriptorName><QualifierName UI="Q000096" MajorTopicYN="N">biosynthesis</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002453" MajorTopicYN="N">Cell Cycle</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002455" MajorTopicYN="N">Cell Division</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002478" MajorTopicYN="N">Cells, Cultured</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D016213" MajorTopicYN="N">Cyclins</DescriptorName><QualifierName UI="Q000096" MajorTopicYN="Y">biosynthesis</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D004790" MajorTopicYN="N">Enzyme Induction</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D004794" MajorTopicYN="N">Enzyme Repression</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005419" MajorTopicYN="N">Flavonoids</DescriptorName><QualifierName UI="Q000096" MajorTopicYN="N">biosynthesis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005656" MajorTopicYN="N">Fungal Proteins</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018506" MajorTopicYN="Y">Gene Expression Regulation, Plant</DescriptorName><QualifierName UI="Q000528" MajorTopicYN="N">radiation effects</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D017343" MajorTopicYN="Y">Genes, Plant</DescriptorName><QualifierName UI="Q000528" MajorTopicYN="N">radiation effects</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006657" MajorTopicYN="N">Histones</DescriptorName><QualifierName UI="Q000096" MajorTopicYN="N">biosynthesis</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D007700" MajorTopicYN="N">Kinetics</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D019684" MajorTopicYN="N">Magnoliopsida</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName><QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName><QualifierName UI="Q000528" MajorTopicYN="Y">radiation effects</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008562" MajorTopicYN="N">Membrane Glycoproteins</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008969" MajorTopicYN="N">Molecular Sequence Data</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005810" MajorTopicYN="N">Multigene Family</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D010446" MajorTopicYN="N">Peptide Fragments</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010650" MajorTopicYN="N">Phenylalanine Ammonia-Lyase</DescriptorName><QualifierName UI="Q000096" MajorTopicYN="N">biosynthesis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010838" MajorTopicYN="N">Phytophthora</DescriptorName><QualifierName UI="Q000472" MajorTopicYN="N">pathogenicity</QualifierName><QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012333" MajorTopicYN="N">RNA, Messenger</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName><QualifierName UI="Q000096" MajorTopicYN="N">biosynthesis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D014158" MajorTopicYN="N">Transcription, Genetic</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D015533" MajorTopicYN="N">Transcriptional Activation</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D014466" MajorTopicYN="Y">Ultraviolet Rays</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1995</Year><Month>12</Month><Day>1</Day></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>1995</Year><Month>12</Month><Day>1</Day><Hour>0</Hour><Minute>1</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>1995</Year><Month>12</Month><Day>1</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">8580959</ArticleId><ArticleId IdType="doi">10.1046/j.1365-313x.1995.8060865.x</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Allemagne</li></country><region><li>District de Cologne</li><li>Rhénanie-du-Nord-Westphalie</li></region><settlement><li>Cologne</li></settlement></list><tree><noCountry><name sortKey="Hahlbrock, K" sort="Hahlbrock, K" uniqKey="Hahlbrock K" first="K" last="Hahlbrock">K. Hahlbrock</name><name sortKey="Schmelzer, E" sort="Schmelzer, E" uniqKey="Schmelzer E" first="E" last="Schmelzer">E. Schmelzer</name><name sortKey="Schroder, J" sort="Schroder, J" uniqKey="Schroder J" first="J" last="Schröder">J. Schröder</name><name sortKey="Somssich, I E" sort="Somssich, I E" uniqKey="Somssich I" first="I E" last="Somssich">I E Somssich</name><name sortKey="Wu, S C" sort="Wu, S C" uniqKey="Wu S" first="S C" last="Wu">S C Wu</name></noCountry><country name="Allemagne"><region name="Rhénanie-du-Nord-Westphalie"><name sortKey="Logemann, E" sort="Logemann, E" uniqKey="Logemann E" first="E" last="Logemann">E. Logemann</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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