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bioRxiv · 10.1101/2024.04.08.588615

CONCERTED PLANT GROWTH AND DEFENSE THROUGH TARGETED PHYTOHORMONE CROSSTALK MODIFICATION

Abstract

Plant immunity activation often results in suppression of plant growth, particularly in the case of constitutive immune activation. We discovered that signaling of the phytohormone cytokinin (CK), known to regulate plant growth through the control of cell division and shoot apical meristem (SAM) activity, can be suppressed by negative crosstalk with the defense phytohormones jasmonic acid (JA), and most evidently, salicylic acid (SA). We show that changing the negative crosstalk of SA on CK signaling in autoimmunity mutants by targeted increase of endogenous CK levels results in plants resistant to pathogens from diverse lifestyles, and relieves suppression of reproductive growth. Moreover, such changes in crosstalk result in a novel reproductive growth phenotype, suggesting a role for defense phytohormones in the SAM, likely through regulation of nitrogen response and cellular redox status. Our data suggest that targeted phytohormone crosstalk engineering can be used to achieve increased reproductive growth and pathogen resistance. SIGNIFICANCE STATEMENTPlants constantly integrate environmental stimuli with developmental programs to optimize their growth and fitness. Excessive activation of the plant immune system often leads to decreased plant growth, a process known as the growth-defense tradeoff. Here, we adapted phytohormone levels in Arabidopsis reproductive tissues of autoimmunity mutants to change phytohormonal crosstalk and diminish the growth tradeoff, resulting in increased broad resistance to pathogens and decreased growth suppression. Similar approaches to phytohormone crosstalk engineering could be used in different contexts to achieve outcomes of higher plant stress resilience and yield.

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BibTeXRIS

Johnston, G. A., Berry, H. M., Kojima, M., Sakakibara, H., Argueso, C. T.. 2024-04-10. CONCERTED PLANT GROWTH AND DEFENSE THROUGH TARGETED PHYTOHORMONE CROSSTALK MODIFICATION. https://doi.org/10.1101/2024.04.08.588615

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