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Updated: Jun 18, 2026

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Lateral Root Inducible System in Arabidopsis and Maize
Published on: January 14, 2016
Genetic variation at bx1 controls DIMBOA content in maize
Ana Butrón1, Y C Chen, G E Rottinghaus
1Misión Biológica de Galiciam,Consejo Superior de Investigaciones Cientificas, Pontevedra, Spain. butron@mbg.cesga.es
Summary
Genetic studies in maize identified quantitative trait loci (QTLs) for 2,4-dihydroxy-7-methoxy-1,4-benzoxazin-3-one (DIMBOA) synthesis, a key compound for insect resistance. While bx1 gene polymorphisms significantly impact DIMBOA levels, the exact causal variants remain elusive.
Area of Science:
- Plant genetics
- Maize breeding
- Biochemistry
Background:
- 2,4-dihydroxy-7-methoxy-1,4-benzoxazin-3-one (DIMBOA) is crucial for maize (Zea mays L.) resistance to corn borers.
- Genes for DIMBOA synthesis are on chromosome 4, a region linked to insect resistance QTLs.
- Previous QTL mapping lacked resolution to confirm bx loci's role in resistance variability.
Purpose of the Study:
- Identify QTLs for DIMBOA synthesis in diverse maize inbreds.
- Assess QTL stability for DIMBOA content across different years.
- Investigate the role of the bx1 gene in DIMBOA variation using association mapping.
Main Methods:
- Utilized eight RIL families from a nested association mapping population.
- Evaluated two RIL families over 2 years to check QTL stability.
- Performed association mapping with 281 diverse inbred lines, focusing on the bx1 gene.
Main Results:
- Identified stable QTLs for DIMBOA content across environments.
- A model with eight markers explained 34% of phenotypic variability in DIMBOA.
- Largest QTL co-localized with DIMBOA pathway genes; bx1 polymorphisms significantly affected DIMBOA content.
Conclusions:
- QTLs for DIMBOA synthesis are stable and linked to the DIMBOA pathway gene cluster.
- Sequence variations in bx1 influence DIMBOA levels in maize.
- The precise causal polymorphisms for the chromosome 4.01 QTL were not identified, possibly due to sequencing limitations, linkage disequilibrium, or multiple causal variants.
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