105
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Heterochromatin influences the secondary metabolite profile in the plant pathogen Fusarium graminearum

      research-article

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Highlights

          ► Heterochromatin protein characterized in F. graminearum. ► Heterochromatic marks regulate secondary metabolism in this fungus. ► Aurofusarin and DON production under Hep1 regulation. ► Surprisingly, Hep1 positively regulates DON biosynthesis. ► Silencing of SM genes by heterochromatin could be conserved mechanism in ascomycetes.

          Abstract

          Chromatin modifications and heterochromatic marks have been shown to be involved in the regulation of secondary metabolism gene clusters in the fungal model system Aspergillus nidulans. We examine here the role of HEP1, the heterochromatin protein homolog of Fusarium graminearum, for the production of secondary metabolites. Deletion of Hep1 in a PH-1 background strongly influences expression of genes required for the production of aurofusarin and the main tricothecene metabolite DON. In the Hep1 deletion strains AUR genes are highly up-regulated and aurofusarin production is greatly enhanced suggesting a repressive role for heterochromatin on gene expression of this cluster. Unexpectedly, gene expression and metabolites are lower for the trichothecene cluster suggesting a positive function of Hep1 for DON biosynthesis. However, analysis of histone modifications in chromatin of AUR and DON gene promoters reveals that in both gene clusters the H3K9me3 heterochromatic mark is strongly reduced in the Hep1 deletion strain. This, and the finding that a DON-cluster flanking gene is up-regulated, suggests that the DON biosynthetic cluster is repressed by HEP1 directly and indirectly. Results from this study point to a conserved mode of secondary metabolite (SM) biosynthesis regulation in fungi by chromatin modifications and the formation of facultative heterochromatin.

          Related collections

          Most cited references57

          • Record: found
          • Abstract: found
          • Article: not found

          Fungal secondary metabolism - from biochemistry to genomics.

          Much of natural product chemistry concerns a group of compounds known as secondary metabolites. These low-molecular-weight metabolites often have potent physiological activities. Digitalis, morphine and quinine are plant secondary metabolites, whereas penicillin, cephalosporin, ergotrate and the statins are equally well known fungal secondary metabolites. Although chemically diverse, all secondary metabolites are produced by a few common biosynthetic pathways, often in conjunction with morphological development. Recent advances in molecular biology, bioinformatics and comparative genomics have revealed that the genes encoding specific fungal secondary metabolites are clustered and often located near telomeres. In this review, we address some important questions, including which evolutionary pressures led to gene clustering, why closely related species produce different profiles of secondary metabolites, and whether fungal genomics will accelerate the discovery of new pharmacologically active natural products.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            VelB/VeA/LaeA complex coordinates light signal with fungal development and secondary metabolism.

            Differentiation and secondary metabolism are correlated processes in fungi that respond to light. In Aspergillus nidulans, light inhibits sexual reproduction as well as secondary metabolism. We identified the heterotrimeric velvet complex VelB/VeA/LaeA connecting light-responding developmental regulation and control of secondary metabolism. VeA, which is primarily expressed in the dark, physically interacts with VelB, which is expressed during sexual development. VeA bridges VelB to the nuclear master regulator of secondary metabolism, LaeA. Deletion of either velB or veA results in defects in both sexual fruiting-body formation and the production of secondary metabolites.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              Scab of Wheat and Barley: A Re-emerging Disease of Devastating Impact

                Bookmark

                Author and article information

                Journal
                Fungal Genet Biol
                Fungal Genet. Biol
                Fungal Genetics and Biology
                Academic Press
                1087-1845
                1096-0937
                January 2012
                January 2012
                : 49
                : 1-3
                : 39-47
                Affiliations
                [a ]Fungal Genetics and Genomics Unit, Department of Applied Genetics and Cell Biology, University of Natural Resources and Life Science Vienna, University and Research Center Campus Tulln-Technopol, Konrad Lorenz Strasse 24, A-3430 Tulln, Austria
                [b ]Health and Environment Department, Austrian Institute of Technology GmbH - AIT, University and Research Center Campus Tulln-Technopol, Konrad Lorenz Strasse 24, A-3430 Tulln, Austria
                [c ]Molecular Plant-Pathogen Interactions, Department of Applied Genetics and Cell Biology, University of Natural Resources and Life Science Vienna, University and Research Center Campus Tulln-Technopol, Konrad Lorenz Strasse 24, A-3430 Tulln, Austria
                [d ]Center for Analytical Chemistry, Department for Agrobiotechnology, University of Natural Resources and Life Science Vienna, University and Research Center Campus Tulln-Technopol, Konrad Lorenz Strasse 24, A-3430 Tulln, Austria
                Author notes
                [* ]Corresponding author at: Fungal Genetics and Genomics Unit, Department of Applied Genetics and Cell Biology, University of Natural Resources and Life Science Vienna, University and Research Center Campus Tulln-Technopol, Konrad Lorenz Strasse 24, A-3430 Tulln, Austria. Fax: +43 1 47654 6392. joseph.strauss@ 123456boku.ac.at
                [1]

                These authors contributed equally for this work.

                Article
                YFGBI2389
                10.1016/j.fgb.2011.11.002
                3278594
                22100541
                91af8d60-475b-4a95-bac0-793063651860
                © 2012 Elsevier Inc.

                This document may be redistributed and reused, subject to certain conditions.

                History
                : 22 June 2011
                : 3 November 2011
                Categories
                Article

                Plant science & Botany
                mycotoxins,secondary metabolism,aurofusarin,fusarium graminearum,heterochromatin protein,deoxynivalenol

                Comments

                Comment on this article