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Breaking the Silence: Protein Stabilization Uncovers Silenced Biosynthetic Gene Clusters in the Fungus Aspergillus nidulans

机译:打破沉默:蛋白质稳定化揭示了构巢曲霉中沉默的生物合成基因簇。

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The genomes of filamentous fungi comprise numerous putative gene clusters coding for the biosynthesis of chemically and structurally diverse secondary metabolites (SMs), which are rarely expressed under laboratory conditions. Previous approaches to activate these genes were based primarily on artificially targeting the cellular protein synthesis apparatus. Here, we applied an alternative approach of genetically impairing the protein degradation apparatus of the model fungus Aspergillus nidulans by deleting the conserved eukaryotic csnE/CSN5 deneddylase subunit of the COP9 signalosome. This defect in protein degradation results in the activation of a previously silenced gene cluster comprising a polyketide synthase gene producing the antibiotic 2,4-dihydroxy-3-methyl-6-(2-oxopropyl)benzaldehyde (DHMBA). The csnE/CSN5 gene is highly conserved in fungi, and therefore, the deletion is a feasible approach for the identification of new SMs.
机译:丝状真菌的基因组包含许多推定的基因簇,这些簇编码化学和结构多样的次生代谢产物(SMs)的生物合成,而这些次生代谢产物很少在实验室条件下表达。激活这些基因的先前方法主要基于人工靶向细胞蛋白质合成装置。在这里,我们应用了另一种方法,通过删除COP9信号小体的保守的真核生物 csnE / CSN5 树枝化酶亚基,遗传损害了模型真菌构巢曲霉的蛋白质降解装置。蛋白质降解的缺陷导致先前沉默的基因簇的激活,该基因簇包含产生抗生素2,4-二羟基-3-甲基-6-(2-氧丙基)苯甲醛(DHMBA)的聚酮化合物合酶基因。 csnE / CSN5 基因在真菌中高度保守,因此,缺失是鉴定新SM的可行方法。

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