Sterols are isoprenoid-derived lipids that play essential structural and functional roles in eukaryotic cells. Plants produce a complex mixture of sterols, and changes in plant sterol profiles have been linked to plant-pathogen interactions. β-Sitosterol and stigmasterol, in particular, have been associated with plant defense. As nematodes have lost the ability to synthesize sterols de novo, they require sterols from the host. Tomato () plants infected by the plant parasitic nematode show a reduced level of stigmasterol and a repression of the gene , encoding the sterol C-22 desaturase that is responsible for the conversion of β-sitosterol to stigmasterol. In this study, we investigated the role of the tomato sterol C-22 desaturase gene in the response to infection by . We explored the plant-nematode interaction over time by analyzing the plant sterol composition and gene regulation in after infection. The temporal gene expression analysis showed that 3 days after inoculation with , the expression was significantly suppressed in the tomato roots, while a significant decrease in the stigmasterol content was observed after 14 days. A knockout mutant tomato line lacking stigmasterol was analyzed to better understand the role of CYP710A11 in nematode development. grown in the mutant line showed reduced egg mass counts, presumably due to the impaired growth of the mutant. However, the nematodes developed as well as they did in the wild-type line. Thus, while the suppression of expression during nematode development may be a defense response of the plant against the nematode, the lack of stigmasterol did not seem to affect the nematode. This study contributes to the understanding of the role of stigmasterol in the interaction between and tomato plants and shows that the sterol C-22 desaturase is not essential for the success of .
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http://dx.doi.org/10.3390/ijms232315111 | DOI Listing |
J Phys Chem B
January 2025
Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, Kraków 30-387, Poland.
Oxidized derivatives of cholesterol play an important role in the functioning of biomembranes. Unlike other biomolecules, which are physiologically active in only one enantiomeric form, some oxysterols exist endogenously as two stereoisomers that exhibit strictly different biological effects. In this paper, we focused our attention on 22-hydroxycholesterol (22-OH) epimers, 22()-OH and 22()-OH, and examined their properties in Langmuir monolayers spread at the air/water interface, using classical surface manometry complemented with Brewster angle microscopy (BAM) images of the film texture.
View Article and Find Full Text PDFNature
August 2024
State Key Laboratory of Plant Environmental Resilience, Frontiers Science Center for Molecular Design Breeding, National Maize Improvement Center, Center for Crop Functional Genomics and Molecular Breeding, Key Laboratory of Biology and Genetic Improvement of Maize (MOA), Beijing Key Laboratory of Crop Genetic Improvement, China Agricultural University, Beijing, China.
Increasing planting density is a key strategy for enhancing maize yields. An ideotype for dense planting requires a 'smart canopy' with leaf angles at different canopy layers differentially optimized to maximize light interception and photosynthesis, among other features. Here we identified leaf angle architecture of smart canopy 1 (lac1), a natural mutant with upright upper leaves, less erect middle leaves and relatively flat lower leaves.
View Article and Find Full Text PDFInt J Mol Sci
March 2024
Laboratory of Biorefinery, Shanghai Advanced Research Institute, Chinese Academy of Sciences, No. 99 Haike Road, Pudong, Shanghai 201210, China.
PeerJ
January 2024
Dongguan Institute of Forestry Science, Dongguan, Guangdong, China.
L. () tuber is a traditional medicinal plant that is abundant in various pharmacological substances. Although diosgenin is commonly found in many Dioscoreaceae plants, its presence in remained uncertain.
View Article and Find Full Text PDFInt J Mol Sci
December 2023
Departamento de Química, Universidad Técnica Federico Santa María, Avenida España 1680, Valparaíso 2340000, Chile.
The synthesis and biological evaluation of brassinosteroids (BRs) analogs with chemical modification in the side alkyl chain is a matter of current interest. Recently, a series of BR analogs with phenyl or benzoate groups in the alkyl chain have been reported. The effect of substitution in the aromatic ring on the biological activities of these new analogs has been evaluated, and the results suggest that the bioactivity is enhanced by substitution with an F atom.
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