Trichothecenes are isoprenoid mycotoxins produced in wheat infected with the filamentous fungus Fusarium graminearum. Some fungal genes for trichothecene biosynthesis (Tri genes) are known to be under control of transcription factors encoded by Tri6 and Tri10. Tri6 and Tri10 deletion mutants were constructed in order to discover additional genes regulated by these factors in planta. Both mutants were greatly reduced in pathogenicity and toxin production and these phenotypes were largely restored by genetic complementation with the wild-type gene. Transcript levels for over 200 genes were altered ≥ twofold for Δtri6 or Δtri10 mutants including nearly all known Tri genes. Also reduced were transcript levels for enzymes in the isoprenoid biosynthetic pathway leading to farnesyl pyrophosphate, the immediate molecular precursor of trichothecenes. DNA sequences 5′ to isoprenoid biosynthetic genes were enriched for the Tri6p DNA binding motif, YNAGGCC, in F. graminearum but not in related species that do not produce trichothecenes. To determine the effect of trichothecene metabolites on gene expression, cultures were treated with trichodiene, the first metabolic intermediate specific to the trichothecene biosynthetic pathway. A total of 153 genes were upregulated by added trichodiene and were significantly enriched for genes likely involved in cellular transport. Differentially regulated genes will be targeted for functional analysis to discover additional factors involved in toxin biosynthesis, toxin resistance and pathogenesis.

Global gene regulation by Fusarium transcription factors Tri6 and Tri10 reveals adaptations for toxin biosynthesis / K. Seong, M. Pasquali, X. Zhou, J. Song, K. Hilburn, S. Mccormick, Y. Dong, J. Xu, H.C. Kistler. - In: MOLECULAR MICROBIOLOGY. - ISSN 0950-382X. - 72:2(2009), pp. 354-367.

Global gene regulation by Fusarium transcription factors Tri6 and Tri10 reveals adaptations for toxin biosynthesis

M. Pasquali
Secondo
;
2009

Abstract

Trichothecenes are isoprenoid mycotoxins produced in wheat infected with the filamentous fungus Fusarium graminearum. Some fungal genes for trichothecene biosynthesis (Tri genes) are known to be under control of transcription factors encoded by Tri6 and Tri10. Tri6 and Tri10 deletion mutants were constructed in order to discover additional genes regulated by these factors in planta. Both mutants were greatly reduced in pathogenicity and toxin production and these phenotypes were largely restored by genetic complementation with the wild-type gene. Transcript levels for over 200 genes were altered ≥ twofold for Δtri6 or Δtri10 mutants including nearly all known Tri genes. Also reduced were transcript levels for enzymes in the isoprenoid biosynthetic pathway leading to farnesyl pyrophosphate, the immediate molecular precursor of trichothecenes. DNA sequences 5′ to isoprenoid biosynthetic genes were enriched for the Tri6p DNA binding motif, YNAGGCC, in F. graminearum but not in related species that do not produce trichothecenes. To determine the effect of trichothecene metabolites on gene expression, cultures were treated with trichodiene, the first metabolic intermediate specific to the trichothecene biosynthetic pathway. A total of 153 genes were upregulated by added trichodiene and were significantly enriched for genes likely involved in cellular transport. Differentially regulated genes will be targeted for functional analysis to discover additional factors involved in toxin biosynthesis, toxin resistance and pathogenesis.
English
graminearum species complex; polyketide synthase genes; encoded fungal toxin; trichothecene biosynthesis; Gibberella-Zeae; insertional mutagenesis; aspergillus-nidulans; alternaria-alternata; ustilago-maydis; wild-type
Settore AGR/12 - Patologia Vegetale
Articolo
Esperti anonimi
Pubblicazione scientifica
2009
72
2
354
367
14
Pubblicato
Periodico con rilevanza internazionale
Aderisco
info:eu-repo/semantics/article
Global gene regulation by Fusarium transcription factors Tri6 and Tri10 reveals adaptations for toxin biosynthesis / K. Seong, M. Pasquali, X. Zhou, J. Song, K. Hilburn, S. Mccormick, Y. Dong, J. Xu, H.C. Kistler. - In: MOLECULAR MICROBIOLOGY. - ISSN 0950-382X. - 72:2(2009), pp. 354-367.
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Article (author)
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K. Seong, M. Pasquali, X. Zhou, J. Song, K. Hilburn, S. Mccormick, Y. Dong, J. Xu, H.C. Kistler
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/439510
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