4.8 Article

Metabolome-Scale Genome-Wide Association Studies Reveal Chemical Diversity and Genetic Control of Maize Specialized Metabolites

期刊

PLANT CELL
卷 31, 期 5, 页码 937-955

出版社

OXFORD UNIV PRESS INC
DOI: 10.1105/tpc.18.00772

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资金

  1. U.S. National Science Foundation [1139329, 1339237]
  2. Graduate Research Fellowship Program [DGE-1650441]
  3. Advanced Research Projects Agency-Energy (ARPA-E), U.S. Department of Energy [DEAR0000598]
  4. Howard Hughes Medical Institute
  5. U.S. Department of Agriculture -Agricultural Research Service
  6. U.S. National Science Foundation (Major Research Instrumentation award) [CHE-1531632]
  7. Direct For Biological Sciences
  8. Division Of Integrative Organismal Systems [1339237] Funding Source: National Science Foundation
  9. Division Of Integrative Organismal Sys
  10. Direct For Biological Sciences [1139329] Funding Source: National Science Foundation

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Cultivated maize (Zea mays) has retained much of the genetic diversity of its wild ancestors. Here, we performed nontargeted liquid chromatography-mass spectrometry metabolomics to analyze the metabolomes of the 282 maize inbred lines in the Goodman Diversity Panel. This analysis identified a bimodal distribution of foliar metabolites. Although 15% of the detected mass features were present in >90% of the inbred lines, the majority were found in <50% of the samples. Whereas leaf bases and tips were differentiated by flavonoid abundance, maize varieties (stiff-stalk, nonstiff-stalk, tropical, sweet maize, and popcorn) showed differential accumulation of benzoxazinoid metabolites. Genome-wide association studies (GWAS), performed for 3,991 mass features from the leaf tips and leaf bases, showed that 90% have multiple significantly associated loci scattered across the genome. Several quantitative trait locus hotspots in the maize genome regulate the abundance of multiple, often structurally related mass features. The utility of maize metabolite GWAS was demonstrated by confirming known benzoxazinoid biosynthesis genes, as well as by mapping isomeric variation in the accumulation of phenylpropanoid hydroxycitric acid esters to a single linkage block in a citrate synthase-like gene. Similar to gene expression databases, this metabolomic GWAS data set constitutes an important public resource for linking maize metabolites with biosynthetic and regulatory genes.

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