A DNA-free genome editing approach using CRISPRi to activate the MYB86 gene in bananas, conferring tolerance to water deficit stress. Built on validated monocot CRISPR/dCas9 tools and prior MYB86 expression studies in yeast and Arabidopsis showing enhanced drought, heat, and salt tolerance.
This solution offers a CRISPRi-based method to activate the MYB86 transcription factor in bananas, aiming to improve tolerance to water deficit stress. Drought is a major constraint on banana cultivation, and activating MYB86 through CRISPRi is proposed to repress secondary metabolite-related gene expression and enhance resilience. The approach is supported by prior lab work showing MYB86 is highly upregulated under drought conditions and that heterologous expression in yeast and Arabidopsis confers improved drought, heat, and salt tolerance. The project targets a DNA-free editing workflow suitable for monocots, with a planned one-year timeline.
The technology is at an early-to-mid development stage. MYB86 isolation, heterologous expression in yeast and Arabidopsis, and CRISPR/dCas9 system development for monocots are already established in the lab. The current proposal focuses on validating MYB86 activation in banana protoplasts and assessing growth and molecular responses under water stress. The team is seeking funding support for research consumables to complete the one-year project plan.
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