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Kokkinopoulou, P.

Publications and source records attributed to Kokkinopoulou, P..

2 recordsLinked to original sources

The SAUERKRAUT transposable element acceleratesArabidopsis floral transition

Salt stress alters plant development, including the floral transition, but regulation of timing of flowering by salt is poorly understood at the molecular level. To identify genetic loci regulating the floral transition under high soil salinity, we performed a genome-wide association study (GWAS) in Arabidopsis thaliana and identified natural variation at the UGT74E1-UGT74E2-BT3 (UUB) locus that correlates with bolting time specifically in response to salt stress. Genetic analysis revealed BT3 as a novel repressor of the floral transition in control conditions. Similarly, the putative IBA glycosylases UGT74E1 & UGT74E2 delay the floral transition in control conditions. Furthermore, we identified that IBA homeostasis regulators TOB1 and ECH2/IBR10 play a key role in the floral transition, and that ECH2/IBR10 are required for the early flowering phenotype of the ugt74e1/ugt74e2 double mutant, indicating that UGT74E1 & UGT74E2 delay flowering by altering IBA homeostasis. A pangenome analysis of the UUB locus revealed variation in the occurrence of the DNA transposon SAUERKRAUT (SKRT). CRISPR-mediated SKRT deletion in Col-0 affected gene expression both within and outside the UUB locus and caused a salt-dependent delayed floral transition. The delayed bolting phenotype of the skrt-2 mutant also depends on ECH2/IBR10 function, indicating that SKRT accelerates the floral transition by altering IBA homeostasis. Finally, targeted demethylation of SKRT resulted in delayed floral transition under salt stress. Taken together, our data show a role for SKRT and its DNA methylation levels in the salt-dependent bolting time response in Arabidopsis, revealing a novel molecular mechanism to control flowering in adverse conditions.

plant biology↗

Quantitative light element (sodium and potassium) profiling in plant tissues using monochromatic X-ray fluorescence analysis

Accurately determining the elemental composition of plant tissues is essential for physiological studies on plant stress, including salinity tolerance. However, high-throughput routine analysis of light elements (range of sodium to calcium) in plant samples is challenging due to the need for complete sample dissolution and expensive inductively coupled plasma-mass-spectrometry (ICP-MS) analysis. Lower costs method (ion chromatography, ion selective electrodes) exists, but also require sample dissolution and lack sensitivity for very small samples (<10 mg). This study reports on a new method for the quantitative analysis of light elements in plant tissues using monochromatic X-ray fluorescence (XRF) instrumentation and innovative sample preparation and mounting. We used this approach to assess elemental uptake, distribution, and accumulation in Arabidopsis thaliana and Oryza sativa plants subjected to salt stress. The method can be used on samples as small as 1 mg making it suitable for small Arabidopsis thaliana plants. We systematically evaluated different sample preparations methods, repeatability, and measurement times to confirm the robustness of the technique. The results show that the monochromatic XRF method delivers rapid, non-destructive, and extraction-free analysis, strongly correlating with ICP-MS acquired data. As such, the monochromatic XRF method is a reliable and efficient alternative for studying salinity tolerance ideally suited for investigating elemental composition of early plant developmental stages, offering new possibilities for research into early stimuli sensing, perception and nutrient efficiency.

plant biology↗