Genetic elucidation of interconnected antibiotic pathways mediating maize innate immunity

被引:60
作者
Ding, Yezhang [1 ]
Weckwerth, Philipp R. [1 ]
Poretsky, Elly [1 ]
Murphy, Katherine M. [2 ]
Sims, James [3 ]
Saldivar, Evan [1 ]
Christensen, Shawn A. [4 ]
Char, Si Nian [5 ]
Yang, Bing [5 ,6 ]
Tong, Anh-dao [1 ]
Shen, Zhouxin [1 ]
Kremling, Karl A. [7 ]
Buckler, Edward S. [7 ,8 ]
Kono, Tom [9 ]
Nelson, David R. [10 ]
Bohlmann, Jorg [11 ]
Bakker, Matthew G. [12 ,13 ]
Vaughan, Martha M. [12 ]
Khalil, Ahmed S. [1 ]
Betsiashvili, Mariam [1 ]
Dressano, Keini [1 ]
Koellner, Tobias G. [14 ]
Briggs, Steven P. [1 ]
Zerbe, Philipp [2 ]
Schmelz, Eric A. [1 ]
Huffaker, Alisa [1 ]
机构
[1] Univ Calif San Diego, Sect Cell & Dev Biol, La Jolla, CA 92093 USA
[2] Univ Calif Davis, Dept Plant Biol, Davis, CA 95616 USA
[3] Swiss Fed Inst Technol, Inst Agr Sci, Zurich, Switzerland
[4] ARS, Chem Res Unit, Ctr Med Agr & Vet Entomol, USDA, Gainesville, FL USA
[5] Univ Missouri, Bond Life Sci Ctr, Div Plant Sci, Columbia, MO USA
[6] Donald Danforth Plant Sci Ctr, St Louis, MO USA
[7] Cornell Univ, Dept Plant Breeding & Genet, Ithaca, NY USA
[8] ARS, Robert W Holley Ctr Agr & Hlth, USDA, New York, NY USA
[9] Univ Minnesota, Minnesota Supercomp Inst, Minneapolis, MN USA
[10] Univ Tennessee, Ctr Hlth Sci, Memphis, TN 38163 USA
[11] Univ British Columbia, Michael Smith Labs, Vancouver, BC, Canada
[12] ARS, Natl Ctr Agr Utilizat Res, USDA, Peoria, IL USA
[13] Univ Manitoba, Dept Microbiol, Winnipeg, MB, Canada
[14] Max Planck Inst Chem Ecol, Jena, Germany
基金
美国国家科学基金会;
关键词
GENOME-WIDE ASSOCIATION; SESQUITERPENE SYNTHASES; QUANTITATIVE RESISTANCE; DEFENSE; FUNGAL; BIOSYNTHESIS; PHYTOALEXINS; MECHANISM; ACCUMULATION; ELICITATION;
D O I
10.1038/s41477-020-00787-9
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Specialized metabolites constitute key layers of immunity that underlie disease resistance in crops; however, challenges in resolving pathways limit our understanding of the functions and applications of these metabolites. In maize (Zea mays), the inducible accumulation of acidic terpenoids is increasingly considered to be a defence mechanism that contributes to disease resistance. Here, to understand maize antibiotic biosynthesis, we integrated association mapping, pan-genome multi-omic correlations, enzyme structure-function studies and targeted mutagenesis. We define ten genes in three zealexin (Zx) gene clusters that encode four sesquiterpene synthases and six cytochrome P450 proteins that collectively drive the production of diverse antibiotic cocktails. Quadruple mutants in which the ability to produce zealexins (ZXs) is blocked exhibit a broad-spectrum loss of disease resistance. Genetic redundancies ensuring pathway resiliency to single null mutations are combined with enzyme substrate promiscuity, creating a biosynthetic hourglass pathway that uses diverse substrates and in vivo combinatorial chemistry to yield complex antibiotic blends. The elucidated genetic basis of biochemical phenotypes that underlie disease resistance demonstrates a predominant maize defence pathway and informs innovative strategies for transferring chemical immunity between crops. In maize, a comprehensive set of approaches enabled the authors to analyse the biosynthetic pathway of the zealexin group of terpenoids and characterize the role of these antibiotic compounds in disease resistance.
引用
收藏
页码:1375 / 1388
页数:14
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