Institute of Food Science and Technology, Chinese Academy of Agricultural Sciences / Key Laboratory of Agro-products Quality and Safety Control in Storage and Transport Process, Ministry of Agriculture and Rural Affairs, Beijing 100193, P. R. China.
J Agric Food Chem. 2024 May 1;72(17):10065-10075. doi: 10.1021/acs.jafc.4c01229. Epub 2024 Apr 18.
Aflatoxins (AFs), highly carcinogenic natural products, are produced by the secondary metabolism of fungi such as . Essential for the fungi to respond to environmental changes and aflatoxin synthesis, the pheromone mitogen-activated protein kinase (MAPK) is a potential regulator of aflatoxin biosynthesis. However, the mechanism by which pheromone MAPK regulates aflatoxin biosynthesis is not clear. Here, we showed Gal83, a new target of Fus3, and identified the pheromone Fus3-MAPK signaling pathway as a regulator of the Snf1/AMPK energy-sensing pathway modulating aflatoxins synthesis substrates. The screening for Fus3 target proteins identified the β subunit of Snf1/AMPK complexes using tandem affinity purification and multiomics. This subunit physically interacted with Fus3 both and and received phosphorylation from Fus3. Although the transcript levels of aflatoxin synthesis genes were not noticeably downregulated in both 83 and 3 deletion mutant strains, the levels of aflatoxin B and its synthesis substrates and gene expression levels of primary metabolizing enzymes were significantly reduced. This suggests that both the Fus3-MAPK and Snf1/AMPK pathways respond to energy signals. In conclusion, all the evidence unlocks a novel pathway of Fus3-MAPK to regulate AFs synthesis substrates by cross-talking with the Snf1/AMPK complexes.
黄曲霉毒素(AFs)是一种高度致癌的天然产物,由真菌如 产生。作为真菌响应环境变化和黄曲霉毒素合成的必要条件,信息素有丝分裂原激活蛋白激酶(MAPK)是黄曲霉毒素生物合成的潜在调节剂。然而,信息素 MAPK 调节黄曲霉毒素生物合成的机制尚不清楚。在这里,我们展示了 Gal83 是 Fus3 的一个新靶点,并确定了信息素 Fus3-MAPK 信号通路作为调节 Snf1/AMPK 能量感应途径的调节剂,从而调节黄曲霉毒素合成底物。通过串联亲和纯化和多组学筛选 Fus3 靶蛋白,鉴定到 Snf1/AMPK 复合物的β亚基。该亚基与 Fus3 在 和 上均发生物理相互作用,并接受 Fus3 的磷酸化。尽管在 83 和 3 缺失突变体菌株中,黄曲霉毒素合成基因的转录水平没有明显下调,但黄曲霉毒素 B 及其合成底物的水平以及初级代谢酶的基因表达水平显著降低。这表明 Fus3-MAPK 和 Snf1/AMPK 途径都对能量信号做出反应。总之,所有证据揭示了一种新的 Fus3-MAPK 途径,通过与 Snf1/AMPK 复合物的串扰来调节 AFs 合成底物。