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Bednarczyk, D.

Publications and source records attributed to Bednarczyk, D..

2 recordsLinked to original sources

ELIP is preferentially expressed in stomatal guard cells and has a role in stomatal opening upon transition to light

Plant early light-induced proteins (ELIPs) are chlorophyll-binding thylakoid membrane proteins commonly believed to function in photoprotection. However, results of studies with mutants or transgenic plants have been contradictory regarding this function, and the mechanistic workings of ELIPs have mostly remained elusive. We studied: (1) ELIP function in tomato (Solanum lycoperiscum) by generation and photosynthetic/physiological characterization of slelip mutants under various light conditions; and (2) ELIP tissue/cell localization by monitoring expression of the Venus yellow fluorescent protein fused to the native SlELIP1 promoter ( pSlELIP1::Venus) in transgenic tomato. Notably, slelip mutants did not display compromised photosynthetic performance and were not more sensitive to photoinhibition compared to parental plants, even following direct sunlight exposure. Surprisingly, pSlELIP1::Venus fusions revealed preferential expression in the leaf epidermis and specifically in stomatal guard cells, with no apparent expression in the mesophyll. No major alterations were observed in leaf gas exchange in slelip mutants at different light conditions. Intriguingly, stomatal conductance was reduced in slelip mutants upon the transition from dark to light. We propose an alternative hypothesis for plant ELIPs as players in the response of guard cells to light, connecting chlorophyll to stomatal function, and presenting a novel research direction for these enigmatic proteins.

plant biology↗

R2R3-MYB EVER links emission of volatiles with epicuticular wax biosynthesis in petunia petal epidermis

The epidermal cells of petunia flowers are the main site of volatile emission. However, data on the mechanisms underlying the release of volatiles into the environment are lacking. Here, using cell-layer-specific transcriptomic analysis, reverse genetics by VIGS and CRISPR, and metabolomics we identified EPIDERMIS VOLATILE EMISSION REGULATOR (EVER)--a petal adaxial epidermis-specific MYB activator that affects the emission of volatiles. Using a three-step viral-based CRISPR/Cas9 editing system, ever knockout lines were generated and together with transient suppression assays, revealed EVERs involvement in the repression of low-vapor-pressure volatiles. Internal pools and annotated scent-related genes involved in production and emission were not affected by EVER. RNA-Seq analyses of petals of ever knockout lines and EVER-overexpressing flowers revealed enrichment in wax-related biosynthesis genes. LC/GC-MS analyses of petal epicuticular waxes revealed substantial reductions in wax loads in ever petals, particularly of monomers of fatty acids and wax esters. These results implicate EVER in the emission of volatiles by fine-tuning the composition of petal epicuticular waxes. Thus, we reveal a petunia MYB regulator that interlinks epicuticular wax composition and volatile emission, thus unraveling a new regulatory layer in the scent-emission machinery in petunia flowers.

plant biology↗