Serveur d'exploration Phytophthora

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Molecular characterization of nucleotide sequences encoding the extracellular glycoprotein elicitor from Phytophthora megasperma.

Identifieur interne : 002B74 ( Main/Exploration ); précédent : 002B73; suivant : 002B75

Molecular characterization of nucleotide sequences encoding the extracellular glycoprotein elicitor from Phytophthora megasperma.

Auteurs : W. Sacks [Allemagne] ; T. Nürnberger ; K. Hahlbrock ; D. Scheel

Source :

RBID : pubmed:7823912

Descripteurs français

English descriptors

Abstract

cDNA sequences encoding the 42 kDa glycoprotein elicitor from the oomycete, Phytophthora megasperma, that induces the defense response in parsley have been cloned and sequenced. The 5' end of the mRNA matches a consensus derived from sequences surrounding the transcription initiation sites of seven other oomycete genes. The major transcript of 1802 nucleotides contains a 529-codon open reading frame, which was predicted to encode a 57 kDa precursor protein. On the basis of peptide sequencing, the N-terminus of the mature protein is at position 163, suggesting that proteolytic processing events, in addition to signal peptide cleavage, generate the protein purified from the fungal culture filtrate. Expression studies in Escherichia coli with the cDNA as well as smaller subfragments demonstrated that a region of 47 amino acids located in the C-terminal third of the protein was sufficient to confer elicitor activity. The gene encoding the elicitor was found to be a member of a multigene family in P. megasperma. Homologous families of differing sizes were found in all eight other Phytophthora species tested, but not in other filamentous fungi including other Oomycetes. No significant similarity of the elicitor preprotein to sequences present in the databases has yet been detected.

DOI: 10.1007/BF00290132
PubMed: 7823912


Affiliations:


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Le document en format XML

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<term>Blotting, Southern (MeSH)</term>
<term>Cloning, Molecular (MeSH)</term>
<term>Coumarins (metabolism)</term>
<term>DNA, Fungal (genetics)</term>
<term>Fungal Proteins (chemistry)</term>
<term>Fungal Proteins (genetics)</term>
<term>Genes, Fungal (MeSH)</term>
<term>Membrane Glycoproteins (chemistry)</term>
<term>Membrane Glycoproteins (genetics)</term>
<term>Molecular Sequence Data (MeSH)</term>
<term>Multigene Family (MeSH)</term>
<term>Phytophthora (genetics)</term>
<term>Plant Extracts (biosynthesis)</term>
<term>Polymerase Chain Reaction (MeSH)</term>
<term>Protein Sorting Signals (genetics)</term>
<term>RNA, Fungal (genetics)</term>
<term>RNA, Messenger (analysis)</term>
<term>Restriction Mapping (MeSH)</term>
<term>Sequence Analysis, DNA (MeSH)</term>
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<term>Terpenes (MeSH)</term>
<term>Vegetables (microbiology)</term>
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<term>Cartographie de restriction (MeSH)</term>
<term>Clonage moléculaire (MeSH)</term>
<term>Coumarines (métabolisme)</term>
<term>Données de séquences moléculaires (MeSH)</term>
<term>Extraits de plantes (biosynthèse)</term>
<term>Famille multigénique (MeSH)</term>
<term>Glycoprotéines membranaires (composition chimique)</term>
<term>Glycoprotéines membranaires (génétique)</term>
<term>Gènes fongiques (MeSH)</term>
<term>Légumes (microbiologie)</term>
<term>Phytophthora (génétique)</term>
<term>Protéines fongiques (composition chimique)</term>
<term>Protéines fongiques (génétique)</term>
<term>Réaction de polymérisation en chaîne (MeSH)</term>
<term>Sesquiterpènes (MeSH)</term>
<term>Signaux de triage des protéines (génétique)</term>
<term>Séquence d'acides aminés (MeSH)</term>
<term>Séquence nucléotidique (MeSH)</term>
<term>Technique de Southern (MeSH)</term>
<term>Terpènes (MeSH)</term>
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<term>Fungal Proteins</term>
<term>Membrane Glycoproteins</term>
<term>Protein Sorting Signals</term>
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<term>Phytophthora</term>
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<term>Phytophthora</term>
<term>Protéines fongiques</term>
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<term>Base Sequence</term>
<term>Blotting, Southern</term>
<term>Cloning, Molecular</term>
<term>Genes, Fungal</term>
<term>Molecular Sequence Data</term>
<term>Multigene Family</term>
<term>Polymerase Chain Reaction</term>
<term>Restriction Mapping</term>
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<term>Sesquiterpenes</term>
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<term>Cartographie de restriction</term>
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<term>Données de séquences moléculaires</term>
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<term>Gènes fongiques</term>
<term>Réaction de polymérisation en chaîne</term>
<term>Sesquiterpènes</term>
<term>Séquence d'acides aminés</term>
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<term>Technique de Southern</term>
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<div type="abstract" xml:lang="en">cDNA sequences encoding the 42 kDa glycoprotein elicitor from the oomycete, Phytophthora megasperma, that induces the defense response in parsley have been cloned and sequenced. The 5' end of the mRNA matches a consensus derived from sequences surrounding the transcription initiation sites of seven other oomycete genes. The major transcript of 1802 nucleotides contains a 529-codon open reading frame, which was predicted to encode a 57 kDa precursor protein. On the basis of peptide sequencing, the N-terminus of the mature protein is at position 163, suggesting that proteolytic processing events, in addition to signal peptide cleavage, generate the protein purified from the fungal culture filtrate. Expression studies in Escherichia coli with the cDNA as well as smaller subfragments demonstrated that a region of 47 amino acids located in the C-terminal third of the protein was sufficient to confer elicitor activity. The gene encoding the elicitor was found to be a member of a multigene family in P. megasperma. Homologous families of differing sizes were found in all eight other Phytophthora species tested, but not in other filamentous fungi including other Oomycetes. No significant similarity of the elicitor preprotein to sequences present in the databases has yet been detected.</div>
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<AbstractText>cDNA sequences encoding the 42 kDa glycoprotein elicitor from the oomycete, Phytophthora megasperma, that induces the defense response in parsley have been cloned and sequenced. The 5' end of the mRNA matches a consensus derived from sequences surrounding the transcription initiation sites of seven other oomycete genes. The major transcript of 1802 nucleotides contains a 529-codon open reading frame, which was predicted to encode a 57 kDa precursor protein. On the basis of peptide sequencing, the N-terminus of the mature protein is at position 163, suggesting that proteolytic processing events, in addition to signal peptide cleavage, generate the protein purified from the fungal culture filtrate. Expression studies in Escherichia coli with the cDNA as well as smaller subfragments demonstrated that a region of 47 amino acids located in the C-terminal third of the protein was sufficient to confer elicitor activity. The gene encoding the elicitor was found to be a member of a multigene family in P. megasperma. Homologous families of differing sizes were found in all eight other Phytophthora species tested, but not in other filamentous fungi including other Oomycetes. No significant similarity of the elicitor preprotein to sequences present in the databases has yet been detected.</AbstractText>
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