首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Bacteria-induced natural product formation in the fungus Aspergillus nidulans requires Saga/ Ada-mediated histone acetylation
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Bacteria-induced natural product formation in the fungus Aspergillus nidulans requires Saga/ Ada-mediated histone acetylation

机译:构巢曲霉中细菌诱导的天然产物形成需要Saga / Ada介导的组蛋白乙酰化

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摘要

Sequence analyses of fungal genomes have revealed that the potential of fungi to produce secondary metabolites is greatly underestimated. In fact, most gene clusters coding for the biosynthesis of antibiotics, toxins, or pigments are silent under standard laboratory conditions. Hence, it is one of the major challenges in microbiology to uncover the mechanisms required for pathway activation. Recently, we discovered that intimate physical interaction of the important model fungus Aspergillus nidulans with the soil-dwelling bacterium Streptomyces rapamycinicus specifically activated silent fungal secondary metabolism genes, resulting in the production of the archetypal polyketide orsellinic acid and its derivatives. Here, we report that the streptomycete triggers modification of fungal histones. Deletion analysis of 36 of 40 acetyltransferases, including histone acetyltransferases (HATs) of A. nidulans, demonstrated that the Saga/Ada complex containing the HAT GcnE and the AdaB protein is required for induction of the orsellinic acid gene cluster by the bacterium. We also showed that Saga/Ada plays a major role for specific induction of other biosynthesis gene clusters, such as sterigmatocystin, terrequinone, and penicillin. Chro-matin immunoprecipitation showed that the Saga/Ada-dependent increase of histone 3 acetylation at lysine 9 and 14 occurs during interaction of fungus and bacterium. Furthermore, the production of secondary metabolites in A. nidulans is accompanied by a global increase in H3K14 acetylation. Increased H3K9 acetylation, however, was only found within gene clusters. This report provides previously undescribed evidence of Saga/Ada dependent histone acetylation triggered by prokaryotes.
机译:真菌基因组的序列分析表明,真菌产生次级代谢产物的潜力被大大低估了。实际上,大多数编码抗生素,毒素或色素生物合成的基因簇在标准实验室条件下都是沉默的。因此,揭示通路激活所需的机制是微生物学的主要挑战之一。最近,我们发现重要的模型真菌构巢曲霉与土壤居住细菌雷帕霉素菌紧密的物理相互作用,特别激活了沉默的真菌次生代谢基因,从而导致了原型聚酮化合物奥地酸及其衍生物的产生。在这里,我们报告链霉菌触发真菌组蛋白的修饰。对40种乙酰基转移酶(包括构巢曲霉的组蛋白乙酰基转移酶(HATs))中的36种进行了缺失分析,结果表明,细菌诱导邻苯二酸基因簇所需的Saga / Ada复合物包含HAT GcnE和AdaB蛋白。我们还表明,Saga / Ada在特异性诱导其他生物合成基因簇(例如sterigmatocystin,terrequinone和青霉素)中起主要作用。染色质的免疫沉淀表明,在真菌和细菌相互作用期间,赖氨酸9和14处Saga / Ada依赖的组蛋白3乙酰化增加。此外,构巢曲霉次生代谢产物的产生伴随着H3K14乙酰化的全球性增加。然而,仅在基因簇内发现增加的H3K9乙酰化。该报告提供了原核生物触发的Saga / Ada依赖性组蛋白乙酰化的先前未描述的证据。

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  • 作者单位

    Departments of Molecular and Applied Microbiology , Leibniz Institute for Natural Product Research and Infection Biology-Hans Knoell Institute, 07745 Jena, Germany Friedrich Schiller University Jena, D-07745 Jena, Germany;

    rnFungal Genetics and Genomics Unit, Department of Applied Genetics and Cell Biology, University of Natural Resources and Life Sciences, Health and Environment Department, A-3430 Tulln, Austria Austrian Institute of Technology GmbH, Health and Environment Department, A-3430 Tulln, Austria;

    rnDepartments of Biomolecular Chemistry, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knoell Institute, 07745 Jena, Germany;

    rnDepartments of Molecular and Applied Microbiology , Leibniz Institute for Natural Product Research and Infection Biology-Hans Knoell Institute, 07745 Jena, Germany;

    rnDepartments of Research Group: Systems Biology/Bioinformatics, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knoell Institute, 07745 Jena, Germany;

    rnFungal Genetics and Genomics Unit, Department of Applied Genetics and Cell Biology, University of Natural Resources and Life Sciences, Health and Environment Department, A-3430 Tulln, Austria Austrian Institute of Technology GmbH, Health and Environment Department, A-3430 Tulln, Austria;

    rnDepartments of Biomolecular Chemistry, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knoell Institute, 07745 Jena, Germany;

    rnFriedrich Schiller University Jena, D-07745 Jena, Germany Departments of Biomolecular Chemistry, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knoell Institute, 07745 Jena, Germany;

    rnFungal Genetics and Genomics Unit, Department of Applied Genetics and Cell Biology, University of Natural Resources and Life Sciences, Health and Environment Department, A-3430 Tulln, Austria Austrian Institute of Technology GmbH, Health and Environment Department, A-3430 Tulln, Austria;

    rnDepartments of Molecular and Applied Microbiology , Leibniz Institute for Natural Product Research and Infection Biology-Hans Knoell Institute, 07745 Jena, Germany Friedrich Schiller University Jena, D-07745 Jena, Germany;

  • 收录信息 美国《科学引文索引》(SCI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    histone modification; microbial communication; secondary metabolism gene clusters;

    机译:组蛋白修饰;微生物交流次生代谢基因簇;
  • 入库时间 2022-08-18 00:40:54

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