Trichothecene 3-O-acetyltransferase protects both the producing organism and transformed yeast from related mycotoxins. Cloning and characterization of Tri101

Trichothecene mycotoxins such as deoxynivalenol, 4,15-diacetoxyscirpenol, and T-2 toxin, are potent protein synthesis inhibitors for eukaryotic organisms. The 3-O-acetyl derivatives of these toxins were shown to reduce their in vitro activity significantly as assessed by assays using a rabbit reticu...

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Published inThe Journal of biological chemistry Vol. 273; no. 3; pp. 1654 - 1661
Main Authors Kimura, M, Kaneko, I, Komiyama, M, Takatsuki, A, Koshino, H, Yoneyama, K, Yamaguchi, I
Format Journal Article
LanguageEnglish
Published United States 16.01.1998
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Abstract Trichothecene mycotoxins such as deoxynivalenol, 4,15-diacetoxyscirpenol, and T-2 toxin, are potent protein synthesis inhibitors for eukaryotic organisms. The 3-O-acetyl derivatives of these toxins were shown to reduce their in vitro activity significantly as assessed by assays using a rabbit reticulocyte translation system. The results suggested that the introduction of an O-acetyl group at the C-3 position in the biosynthetic pathway works as a resistance mechanism for Fusarium species that produce t-type trichothecenes (trichothecenes synthesized via the precursor trichotriol). A gene responsible for the 3-O-acetylation reaction, Tri101, has been successfully cloned from a Fusarium graminearum cDNA library that was designed to be expressed in Schizosaccharomyces pombe. Fission yeast transformants were selected for their ability to grow in the presence of T-2 toxin, and this strategy allowed isolation of 25 resistant clones, all of which contained a cDNA for Tri101. This is the first drug-inactivating O-acetyltransferase gene derived from antibiotic-producing organisms. The open reading frame of Tri101 codes for a polypeptide of 451 amino acid residues, which shows no similarity to any other proteins reported so far. TRI101 from recombinant Escherichia coli catalyzes O-acetylation of the trichothecene ring specifically at the C-3 position in an acetyl-CoA-dependent manner. By using the Tri101 cDNA as a probe, two least overlapping cosmid clones that cover a region of 70 kilobase pairs have been isolated from the genome of F. graminearum. Other trichothecene biosynthetic genes, Tri4, Tri5, and Tri6, were not clustered in the region covered by these cosmid clones. These new cosmid clones are considered to be located in other parts of the large biosynthetic gene cluster and might be useful for the study of trichothecene biosynthesis.
AbstractList Trichothecene mycotoxins such as deoxynivalenol, 4,15-diacetoxyscirpenol, and T-2 toxin, are potent protein synthesis inhibitors for eukaryotic organisms. The 3-O-acetyl derivatives of these toxins were shown to reduce their in vitro activity significantly as assessed by assays using a rabbit reticulocyte translation system. The results suggested that the introduction of an O-acetyl group at the C-3 position in the biosynthetic pathway works as a resistance mechanism for Fusarium species that produce t-type trichothecenes (trichothecenes synthesized via the precursor trichotriol). A gene responsible for the 3-O-acetylation reaction, Tri101, has been successfully cloned from a Fusarium graminearum cDNA library that was designed to be expressed in Schizosaccharomyces pombe. Fission yeast transformants were selected for their ability to grow in the presence of T-2 toxin, and this strategy allowed isolation of 25 resistant clones, all of which contained a cDNA for Tri101. This is the first drug-inactivating O-acetyltransferase gene derived from antibiotic-producing organisms. The open reading frame of Tri101 codes for a polypeptide of 451 amino acid residues, which shows no similarity to any other proteins reported so far. TRI101 from recombinant Escherichia coli catalyzes O-acetylation of the trichothecene ring specifically at the C-3 position in an acetyl-CoA-dependent manner. By using the Tri101 cDNA as a probe, two least overlapping cosmid clones that cover a region of 70 kilobase pairs have been isolated from the genome of F. graminearum. Other trichothecene biosynthetic genes, Tri4, Tri5, and Tri6, were not clustered in the region covered by these cosmid clones. These new cosmid clones are considered to be located in other parts of the large biosynthetic gene cluster and might be useful for the study of trichothecene biosynthesis.
Author Yamaguchi, I
Yoneyama, K
Komiyama, M
Kaneko, I
Kimura, M
Takatsuki, A
Koshino, H
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Snippet Trichothecene mycotoxins such as deoxynivalenol, 4,15-diacetoxyscirpenol, and T-2 toxin, are potent protein synthesis inhibitors for eukaryotic organisms. The...
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SubjectTerms ACETILACION
ACETYLATION
Acetyltransferases - chemistry
Acetyltransferases - genetics
Acetyltransferases - metabolism
ACILTRANSFERASA
ACTIVIDAD ENZIMATICA
ACTIVITE ENZYMATIQUE
ACYLTRANSFERASE
ACYLTRANSFERASES
ADN
Amino Acid Sequence
AMINO ACID SEQUENCES
Animals
Base Sequence
Cell Line
CHEMICAL COMPOSITION
CLONACION
CLONAGE
CLONING
Cloning, Molecular
COMPLEMENTARY DNA
COMPOSICION QUIMICA
COMPOSITION CHIMIQUE
Cricetinae
CYTOTOXICITY
DNA
ENZYMIC ACTIVITY
EXPRESION GENICA
EXPRESSION DES GENES
GENBANK/AB000874
GENE
GENE EXPRESSION
GENE TRANSFER
GENES
GENETIC TRANSFORMATION
GENETICA
GENETICS
GENETIQUE
GIBBERELLA ZEAE
Models, Chemical
MOLECULAR MAPPING
MOLECULAR SEQUENCE DATA
Mycotoxins - pharmacology
NUCLEOTIDE SEQUENCE
OPEN READING FRAMES
Plasmids - drug effects
PROTECTION
Rabbits
RESTRICTION MAPPING
SCHIZOSACCHAROMYCES POMBE
SECUENCIA NUCLEOTIDICA
SEQUENCE NUCLEOTIDIQUE
STRUCTURAL GENES
T-2 Toxin - pharmacology
TOXICIDAD
TOXICITE
TOXICITY
TRANSFERENCIA DE GENES
TRANSFERT DE GENE
TRANSFORMACION GENETICA
TRANSFORMATION GENETIQUE
TRI101 GENE
TRICHOTHECENE
TRICHOTHECENES
Trichothecenes - biosynthesis
Title Trichothecene 3-O-acetyltransferase protects both the producing organism and transformed yeast from related mycotoxins. Cloning and characterization of Tri101
URI https://www.ncbi.nlm.nih.gov/pubmed/9430709
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Volume 273
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