Arbuscular mycorrhizas (AMs) are divided into two types according to morphology: Arum- and Paris-type AMs. Gibberellins (GAs) mainly inhibit the establishment of Arum-type AM symbiosis in most model plants, whereas the effects of GAs on Paris-type AM symbiosis are unclear. To provide insight into the mechanism underlying this type of symbiosis, the roles of GAs were investigated in Eustoma grandiflorum when used as the host plant for Paris-type AM establishment. Eustoma grandiflorum seedlings were inoculated with the model AM fungus, Rhizophagus irregularis, and the effects of GA and the GA biosynthesis inhibitor uniconazole-P on the symbiosis were quantitatively evaluated. Exogenous GA significantly increased hyphopodium formation at the epidermis, thus leading to the promotion of fungal colonization and arbuscule formation in the root cortex. By contrast, the suppression of GA biosynthesis and signaling attenuated fungal entry to E. grandiflorum roots. Moreover, the exudates from GA-treated roots strongly induced the hyphal branching of R. irregularis. Our results show that GA has an contrasting effect on Paris-type AM symbiosis in E. grandiflorum compared with Arum-type AM symbiosis. This finding could be explained by the differential regulation of the early colonization stage, where fungal hyphae make contact with and penetrate the epidermis.
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http://dx.doi.org/10.1093/pcp/pcz222 | DOI Listing |
Curr Opin Plant Biol
December 2024
Faculty of Agriculture, Tottori University, Koyama Minami, Tottori 680-8553, Japan. Electronic address:
J Econ Entomol
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Key Laboratory of Surveillance and Management of Invasive Alien Species in Guizhou Education Department, Guizhou Provincial Key Laboratory for Rare Animal and Economic Insect of the Mountainous Region, Department of Biology and Engineering of Environment, Guiyang University, Guiyang, China.
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Key Laboratory of Saline-alkali Vegetation Ecology Restoration (Northeast Forestry University), Ministry of Education, Harbin 150040, China.
The optimization of the CRISPR-Cas9 system for enhancing editing efficiency holds significant value in scientific research. In this study, we optimized single guide RNA and promoters of the CRISPR-Cas9 vector and established an efficient protoplast isolation and transient transformation system in , and we successfully applied the modified CRISPR-Cas9 system to detect editing efficiency of the gene. The activity of the promoter in protoplasts was approximately three times higher than that of the promoter.
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Faculty of Agriculture, Tottori University, Tottori 680-8553, Japan.
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Mississippi State University, Biochemistry, Molecular Biology, Entomology and Plant Pathology, 100 Twelve Lane, Mail Stop 9775, Mississippi State, Mississippi, United States, 39762;
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