Department of Genetics, University of Wisconsin-Madison, Madison, WI 53706, United States.
Department of Microbiology and Immunology, University of Wisconsin-Madison, Madison, WI 53706, United States; Department of Bacteriology, University of Wisconsin-Madison, Madison, WI 53706, United States.
Biotechnol Adv. 2019 Nov 1;37(6):107345. doi: 10.1016/j.biotechadv.2019.02.001. Epub 2019 Feb 7.
Fungi produce an abundance of bioactive secondary metabolites which can be utilized as antibiotics and pharmaceutical drugs. The genes encoding secondary metabolites are contiguously arranged in biosynthetic gene clusters (BGCs), which supports co-regulation of all genes required for any one metabolite. However, an ongoing challenge to harvest this fungal wealth is the finding that many of the BGCs are 'silent' in laboratory settings and lie in heterochromatic regions of the genome. Successful approaches allowing access to these regions - in essence converting the heterochromatin covering BGCs to euchromatin - include use of epigenetic stimulants and genetic manipulation of histone modifying proteins. This review provides a comprehensive look at the chromatin remodeling proteins which have been shown to regulate secondary metabolism, the use of chemical inhibitors used to induce BGCs, and provides future perspectives on expansion of epigenetic tools and concepts to mine the fungal metabolome.
真菌产生大量生物活性的次级代谢产物,可被用作抗生素和药物。编码次级代谢产物的基因在生物合成基因簇(BGCs)中连续排列,这支持了所有代谢产物所需基因的共同调控。然而,从真菌中获取这些财富的一个持续挑战是发现许多 BGC 在实验室环境中是“沉默的”,并且位于基因组的异染色质区域。成功的方法可以访问这些区域——实质上是将覆盖 BGC 的异染色质转化为常染色质——包括使用表观遗传刺激剂和组蛋白修饰蛋白的遗传操作。这篇综述全面介绍了已被证明能调节次级代谢的染色质重塑蛋白,以及用于诱导 BGC 的化学抑制剂,并对扩展表观遗传工具和概念以挖掘真菌代谢组提供了未来的展望。