Fusarium-Induced Shoot Elongation Correlates with Seedling Lodging Rate and Root Reduction Natural Variation in Fusarium-Induced Morphological Changes.

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15 The Genetic Basis of Complex Inheritance
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Fusarium-Induced Shoot Elongation Correlates with Seedling Lodging Rate and Root Reduction Natural Variation in Fusarium-Induced Morphological Changes Error bars = standard errors Metabolic Profiles Constitutive and Fusarium-Infected Roots Differ Among Maize Inbred Lines Each circle represents a significantly changed mass fragment comparing roots inoculated with strain Gz014 spores and mock inoculum. Color of circles: up (green) or down (red) regulation upon fungal infection; intensity of color: p value calculated from one-way ANOVA; size of circles: fold change. DIM 2 BOA is significantly different between constitutive B73 and Mo17 roots, and is significantly changed in B73 roots upon F. graminearum inoculation. QTL mapping of constitutive DIM 2 BOA content in seedling roots identifies a novel benzoxazinoid biosynthetic gene. QTL mapping of metabolites with contrasting constitutive content in B73 and Mo17 roots identifies a few genomic hotspots simultaneous regulating multiple metabolites. Future Perspectives Purify and identify putative F. graminearum resistance-related compounds, and test for in vitro effect on fungal growth. Combine QTL mapping results with a transcriptomics study to identify candidate genes and validate with near isogeneic lines, transposon insertion lines, and/or heterologous expression. Introduction Fusarium graminearum is one of the most destructive and widespread fungal pathogens attacking small grain crops. In maize, it is a major concern for contaminating kernels with mycotoxins, as well as infecting stems (Gibberella stem rot) and seedlings (Gibberella seedling blight). Previous genetic mapping efforts for resistance in maize have identified a large number of environment-dependent quantitative trait loci (QTL) with small effect size. In this project, we focus on a less studied developmental stage (V3 seedlings) and tissue type (roots) in maize-F. graminearum interaction studies, use better defined and quantitative traits, and perform artificial inoculation experiment with diverse maize and fungal genotypes in controlled growth chambers. We evaluate the natural variation in morphological changes induced by F. graminearum root infection, and take a comparative approach to identify potential biochemical component of resistance. These studies provide data for future genetic mapping of resistance against F. graminearum in maize seedlings. Fusarium Reduces Roots and Elongates Shoots of Maize Seedlings Seedlings inoculated with F. graminearum spore suspension (4.5x10 5 /mL) when primary roots reached ~9 cm. Pictures taken 6 days post inoculation. Natural Variation in Fusarium graminearum Induced Changes in Maize Seedlings Shaoqun Zhou 1,2, Meena Haribal 2, Gary Bergstrom 1, and Georg Jander 2 1 School of Integrative Plant Sciences, Cornell University, Ithaca, NY 2 Boyce Thompson Institute for Plant Research, Ithaca, NY Goals 1.Explore the natural variation in F. graminearum induced plant morphological changes using diverse plant and fungal genotypes, and test for correlation between these changes. 2.Compare metabolic profiles of maize genotypes showing contrasting morphological changes in response to F. graminearum infection to identify potential biochemical components of fungal resistance. 3.Investigate the genetic control of F. graminearum-induced morphological changes and dynamics of potentially resistance-related compounds. Acknowledgement Part of this project is funded by Northeast Sustainable Agriculture Research & Education Graduate Student Grant, Project Number GNE F. graminearum strains used in this project are generous gifts from Dr. Gary Bergstrom. Commercial maize hybrids are kindly provided by Blue River Hybrids Organic Seed. Training for root measurement with RootReader2D platform was provided by Dr. Eric Craft. B73 NC358 MockStrain Gz014 MockStrain Gz014 B73 Mo17 Mock (Constitutive)Gz014 (Induced) Mo17 NC350 NC358 B73 m/z Retention Time/min R 2 = R 2 = PC1 – Variance 40% PC1 – Variance 44% PC2 – Variance 21% PC2 – Variance 16% Handrick et al., Submitted DIMBOA-Glc TRIMBOA-Glc DIM 2 BOA-Glc Chromosome no. Number of QTLs