Wiemann Philipp, Brown Daren W, Kleigrewe Karin, Bok Jin Woo, Keller Nancy P, Humpf Hans-Ulrich, Tudzynski Bettina
Institut für Botanik, Westfälische Wilhelms-Universität Münster, Schlossgarten 3, D-48149 Münster, GermanyInstitut für Lebensmittelchemie, Westfälische Wilhelms-Universität Münster, Corrensstraße 45, D-48149 Münster, GermanyBacterial Foodborne Pathogens and Mycology Research, USDA/ARS, 1815 N University St, Peoria, IL 61604, USADepartment of Medical Microbiology and ImmunologyDepartment of Bacteriology, University of Wisconsin, 1550 Linden Dr, Madison, WI 53706-1521, USA.
Mol Microbiol. 2010 Aug;77(4):972-94. doi: 10.1111/j.1365-2958.2010.07263.x. Epub 2010 Jun 21.
Besides industrially produced gibberellins (GAs), Fusarium fujikuroi is able to produce additional secondary metabolites such as the pigments bikaverin and neurosporaxanthin and the mycotoxins fumonisins and fusarin C. The global regulation of these biosynthetic pathways is only poorly understood. Recently, the velvet complex containing VeA and several other regulatory proteins was shown to be involved in global regulation of secondary metabolism and differentiation in Aspergillus nidulans. Here, we report on the characterization of two components of the F. fujikuroi velvet-like complex, FfVel1 and FfLae1. The gene encoding this first reported LaeA orthologue outside the class of Eurotiomycetidae is upregulated in ΔFfvel1 microarray-studies and FfLae1 interacts with FfVel1 in the nucleus. Deletion of Ffvel1 and Fflae1 revealed for the first time that velvet can simultaneously act as positive (GAs, fumonisins and fusarin C) and negative (bikaverin) regulator of secondary metabolism, and that both components affect conidiation and virulence of F. fujikuroi. Furthermore, the velvet-like protein FfVel2 revealed similar functions regarding conidiation, secondary metabolism and virulence as FfVel1. Cross-genus complementation studies of velvet complex component mutants between Fusarium, Aspergillus and Penicillium support an ancient origin for this complex, which has undergone a divergence in specific functions mediating development and secondary metabolism.
除了工业生产的赤霉素(GAs)外,藤仓镰孢还能够产生其他次生代谢产物,如色素红曲菌素和神经孢菌黄素,以及霉菌毒素伏马菌素和镰刀菌素C。目前对这些生物合成途径的全局调控了解甚少。最近,含有VeA和其他几种调控蛋白的 velvet 复合体被证明参与了构巢曲霉次生代谢和分化的全局调控。在此,我们报道了藤仓镰孢 velvet 样复合体的两个组分FfVel1和FfLae1的特性。在ΔFfvel1芯片研究中,编码首次报道的类 Eurotiomycetidae 以外的LaeA直系同源物的基因上调,并且FfLae1在细胞核中与FfVel1相互作用。Ffvel1和Fflae1的缺失首次揭示,velvet 可以同时作为次生代谢的正调控因子(GAs、伏马菌素和镰刀菌素C)和负调控因子(红曲菌素),并且这两个组分都影响藤仓镰孢的分生孢子形成和毒力。此外,velvet 样蛋白FfVel2在分生孢子形成、次生代谢和毒力方面显示出与FfVel1相似得功能。镰刀菌属、曲霉属和青霉属之间的 velvet 复合体组分突变体的跨属互补研究支持了该复合体起源古老,其在介导发育和次生代谢的特定功能上发生了分化。