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Weinstain, R.

Publications and source records attributed to Weinstain, R..

5 recordsLinked to original sources

Spatially-restricted metabolic delivery of auxin for selective adventitious root induction

Auxin impacts on nearly every aspect of plant growth and development. Its exogenous application therefore results in pleiotropic growth responses. Exploiting this activity for plant propagation requires avoiding or minimizing such off-target effects and is generally achieved as a trade-off between toxicity and organogenetic efficacity. We recently identified the compound HYSPARIN (HYS) with potent, and uniquely selective adventitious root inductive activity. Unlike other root-inducing compounds, HYS preferentially activates auxin responses in the shoot via an unknown mechanism. Here, we show that HYS acts as a shoot-specific proauxin. Rather than acting through auxin homeostasis, we found that HYS is hydrolysed in planta independently of ILR1/ILL amidohydrolases to release the synthetic auxin MCPA. Structure-activity relationship analysis confirmed a strong dependence on its MCPA moiety for activating auxin responses, and identified its promoiety as a determinant of shoot-specificity and activity. Selective application of MCPA also potently induces AR is consistent with a model in which HYS metabolism produces a spatially restricted, AR inductive auxin signal. The activation mechanism of HYS thus provides a conceptual framework for tissue-specific metabolic delivery of auxin and may enable the programmable delivery of other xenobiotics in plants.

plant biology↗

Triphenylphosphonium is an effective targeting moiety for plants mitochondria

Small signaling molecule regulates key physiological processes in plants, often in a spatially distinct manner. However, current methods for applying small-molecules, endogenous or synthetic, in plants research lack spatial precision, limiting the ability to study and utilize their localized effects. Here, we validate triphenylphosphonium (TPP) as a mitochondrial targeting motif in plants. Using fluorescently labeled TPP conjugates in Arabidopsis thaliana, we demonstrate mitochondria-specific accumulation, even in the presence of plastids. This precise localization enables detailed imaging of mitochondria and mitochondrial DNA in living plants. We further exploit this targeting ability by developing a TPP-ciprofloxacin conjugate to selectively inhibit mitochondrial DNA gyrase, an enzyme involved in organellar DNA replication. Unlike free ciprofloxacin, which disrupts both mitochondrial and chloroplast DNA gyrase activity, the TPP-conjugate specifically targets mitochondrial gyrase, leading to slower plant growth without affecting chloroplast function. This targeted inhibition triggers a mitochondrial retrograde response, characterized by increased reactive oxygen species levels and the upregulation of stress-response genes in the nucleus. Our findings establish TPP as a reliable tool for mitochondrial targeting in plants and open avenues for both fundamental research and agricultural applications. By enabling organelle-specific manipulation in species not amenable to genetic engineering, TPP-based strategies have potential for advancing plant biology and precision agriculture.

plant biology↗

Alleviating the barrier of adventitious roots formation in recalcitrant mature tissue by slow release of a synthetic auxin

Clonal propagation of plants by induction of adventitious roots (ARs) from stem cuttings is a requisite step in breeding programs. A major barrier exists for propagating valuable plants that naturally have low capacity to form ARs. Due to the central role of auxin in organogenesis, indole-3-butyric acid (IBA) is often used as part of commercial rooting mixtures, yet many recalcitrant plants do not form ARs in response to this treatment. Here, we describe the synthesis and screening of a focused library of synthetic auxin conjugates in Eucalyptus grandis cuttings and identify 4-chlorophenoxyacetic acid-L-tryptophan-OMe as a competent enhancer of adventitious rooting in a number of recalcitrant woody plants, including apple and argan. Comprehensive metabolic and functional analyses reveal that this activity is engendered by prolonged auxin signaling due to initial fast uptake and slow release and clearance of the free auxin 4-chlorophenoxyacetic acid. This work highlights the utility of a slow-release strategy for bioactive compounds for more effective plant growth regulation.

plant biology↗

A quantitative gibberellin signalling biosensor reveals a role for gibberellins in internode specification at the shoot apical meristem

Growth at the shoot apical meristem (SAM) is essential for shoot architecture construction. The phytohormones gibberellins (GA) play a pivotal role in coordinating plant growth, but their role in the SAM remains mostly unknown. Here, we developed a ratiometric GA signalling biosensor by engineering one of the DELLA proteins, to suppress its master regulatory function in GA transcriptional responses while preserving its degradation upon GA sensing. We demonstrate that this novel degradation-based biosensor accurately reports on cellular changes in GA levels and perception during development. We used this biosensor to map GA signalling activity in the SAM. We show that high GA signalling is found primarily in cells located between organ primordia that are the precursors of internodes. By gain- and loss-of-function approaches, we further demonstrate that GAs regulate cell division plane orientation to establish the typical cellular organisation of internodes, thus contributing to internode specification in the SAM.

plant biology↗

ABA homeostasis and long-distance translocation is redundantly regulated by ABCG ABA importers

The effects of abscisic acid (ABA) on plant growth, development and response to the environment depend on local ABA concentrations. Here, we exploited a genome-scale amiRNA screen, targeting the Arabidopsis transportome, to show that ABA homeostasis is regulated by two previously unknown ABA transporters. ABCG17 and ABCG18 are localized to the plasma membranes of leaf mesophyll and stem cortex cells to redundantly promote ABA import, leading to conjugated inactive ABA sinks, thus restricting stomatal closure. ABCG17 and ABCG18 double knockdown revealed that the transporters encoded by these genes not only limit stomatal aperture size, conductance and transpiration while increasing water-use efficiency but also control ABA translocation from the shoot to the root to regulate lateral root emergence. The proposed ABCG17- and ABCG18-dependent ABA glucosyl ester shoot sink mechanism is restrained under abiotic stress conditions to further activate the ABA responses.

plant biology↗