Helmholtz International Lab for Anti-Infectives, Shandong University-Helmholtz Institute of Biotechnology, State Key Laboratory of Microbial Technology, Shandong University, Qingdao, 266237, China.
The College of Life Sciences, Key Laboratory of Pesticide and Chemical Biology, Ministry of Education, Central China Normal University, Wuhan, 430079, China.
Microb Biotechnol. 2021 Sep;14(5):1918-1930. doi: 10.1111/1751-7915.13834. Epub 2021 Jun 17.
Med-ORF10, a single-domain protein with unknown function encoded by a gene located in a gene cluster responsible for the biosynthesis of a novel antitumour antibiotic medermycin, shares high homology to a group of small proteins widely distributed in many aromatic polyketide antibiotic pathways. This group of proteins contain a nuclear transport factor-2 (NTF-2) domain and appear to undergo an evolutionary divergence in their functions. Gene knockout and interspecies complementation suggested that Med-ORF10 plays a regulatory role in medermycin biosynthetic pathway. Overexpression of med-ORF10 in its wild-type strain led to significant increase of medermycin production. It was also shown by qRT-PCR and Western blot that Med-ORF10 controls the expression of genes encoding tailoring enzymes involved in medermycin biosynthesis. Transcriptome analysis and qRT-PCR revealed that Med-ORF10 has pleiotropic effects on more targets. However, there is no similar conserved domain available in Med-ORF10 compared to those of mechanistically known regulatory proteins; meanwhile, no direct interaction between Med-ORF10 and its target promoter DNA was detected via gel shift assay. All these studies suggest that Med-ORF10 regulates medermycin biosynthesis probably via an indirect mode.
Med-ORF10 是一种单结构域蛋白,其功能未知,由一个基因编码,该基因位于负责合成新型抗肿瘤抗生素美替拉霉素的基因簇中。该蛋白与广泛分布于许多芳香聚酮类抗生素途径中的一组小蛋白具有高度同源性。这组蛋白包含核转运因子-2(NTF-2)结构域,其功能似乎发生了进化分歧。基因敲除和种间互补实验表明,Med-ORF10 在美替拉霉素生物合成途径中发挥调控作用。在其野生型菌株中过表达 med-ORF10 会导致美替拉霉素产量显著增加。qRT-PCR 和 Western blot 也表明 Med-ORF10 控制参与美替拉霉素生物合成的修饰酶基因的表达。转录组分析和 qRT-PCR 显示 Med-ORF10 对更多靶标具有多效性影响。然而,与机制上已知的调节蛋白相比,Med-ORF10 中没有类似的保守结构域;同时,凝胶迁移实验也没有检测到 Med-ORF10 与其靶启动子 DNA 之间的直接相互作用。所有这些研究表明,Med-ORF10 可能通过间接模式调节美替拉霉素的生物合成。