TY - INPR ID - 2325 TI - Shoot-to-root translocation of the jasmonate precursor 12-oxo-phytodienoic acid (OPDA) coordinates plant growth responses following tissue damage JO - bioRxiv PY - 2019 SP - AU - Schulze, A. AU - Zimmer, M. AU - Mielke, S. AU - Stellmach, H. AU - Melnyk, C. W. AU - Hause, B. AU - Gasperini, D. VL - UR - https://doi.org/10.1101/517193 DO - 10.1101/517193 AB - Multicellular organisms rely upon the movement of signaling molecules across cells, tissues and organs to communicate among distal sites. In plants, herbivorous insects, necrotrophic pathogens and mechanical wounding stimulate the activation of the jasmonate (JA) pathway, which in turn triggers the transcriptional changes necessary to protect plants against those challenges, often at the expense of growth. Although previous evidence indicated that JA species can translocate from damaged into distal sites, the identity of the mobile compound(s), the tissues through which they translocate and the consequences of their relocation remain unknown. Here, we demonstrated that endogenous JA species generated after shoot injury translocate to unharmed roots via the phloem vascular tissue in Arabidopsis thaliana. By wounding wild-type shoots of chimeric plants and by quantifying the relocating compounds from their JA-deficient roots, we uncovered that the JA-Ile precursor 12-oxo-phytodienoic acid (OPDA) is a mobile JA species. Our data also showed that OPDA is a primary mobile compound relocating to roots where, upon conversion to the bioactive hormone, it induces JA-mediated gene expression and root growth inhibition. Collectively, our findings reveal the existence of long-distance transport of endogenous OPDA which serves as a communication molecule to coordinate shoot-to-root responses, and highlight the importance of a controlled distribution of JA species among organs during plant stress acclimation. A2 - C1 - Molecular Signal Processing; Cell and Metabolic Biology ER - TY - INPR ID - 2248 TI - Photoperiod sensing of the circadian clock is controlled by ELF3 and GI JO - BioRxiv PY - 2018 SP - AU - Anwer, U. AU - Davis, A. AU - Davis, S. J. AU - Quint, M. VL - UR - https://doi.org/10.1101/321794 DO - 10.1101/321794 AB - ELF3 and GI are two important components of the Arabidopsis circadian clock. They are not only essential for the oscillator function but are also pivotal in mediating light inputs to the oscillator. Lack of either results in a defective oscillator causing severely compromised output pathways, such as photoperiodic flowering and hypocotyl elongation. Although single loss of function mutants of ELF3 and GI have been well-studied, their genetic interaction remains unclear. We generated an elf3 gi double mutant to study their genetic relationship in clock-controlled growth and phase transition phenotypes. We found that ELF3 and GI repress growth during the night and the day, respectively. We also provide evidence that ELF3, for which so far only a growth inhibitory role has been reported, can also act as a growth promoter under certain conditions. Finally, circadian clock assays revealed that ELF3 and GI are essential Zeitnehmers that enable the oscillator to synchronize the endogenous cellular mechanisms to external environmental signals. In their absence, the circadian oscillator fails to synchronize to the light-dark cycles even under diurnal conditions. Consequently, clock-mediated photoperiod-responsive growth and development is completely lost in plants lacking both genes, suggesting that ELF3 and GI together convey photoperiod sensing to the central oscillator. Since ELF3 and GI are conserved across flowering plants and represent important breeding and domestication targets, our data highlight the possibility of developing photoperiod-insensitive crops by manipulating the combination of these two key genes. A2 - C1 - Molecular Signal Processing ER - TY - INPR ID - 2275 TI - New Light on Local and Systemic Wound Signaling JO - Trends Plant Sci PY - 2018 SP - AU - Wasternack, C. VL - UR - https://dx.doi.org/10.1016/j.tplants.2018.11.009 DO - 10.1016/j.tplants.2018.11.009 AB - Electric signaling and Ca2+ waves were discussed to occur in systemic wound responses. Two new overlapping scenarios were identified: (i) membrane depolarization in two special cell types followed by an increase in systemic cytoplasmic Ca2+ concentration ([Ca2+]cyt), and (ii) glutamate sensed by GLUTAMATE RECEPTOR LIKE proteins and followed by Ca2+-based defense in distal leaves. A2 - C1 - Molecular Signal Processing ER - TY - INPR ID - 2277 TI - The Local Phosphate Deficiency Response Activates ER Stress-dependent Autophagy JO - Plant Physiol PY - 2018 SP - pp.01379.2018 AU - Naumann, C. AU - Müller, J. AU - Sakhonwasee, S. AU - Wieghaus, A. AU - Hause, G. AU - Heisters, M. AU - Bürstenbinder, K. AU - Abel, S. VL - UR - https://dx.doi.org/10.1104/pp.18.01379 DO - 10.1104/pp.18.01379 AB - Inorganic phosphate (Pi) is often a limiting plant nutrient. In members of the Brassicaceae family, such as Arabidopsis thaliana, Pi deprivation reshapes root system architecture to favor topsoil foraging by inhibiting primary root extension and stimulating lateral root formation. Root growth inhibition upon Pi deficiency is triggered by Fe-stimulated, apoplastic ROS generation and cell wall modifications, which impair cell-to-cell communication and meristem maintenance. These processes require LPR1 (LOW PHOSPHATE RESPONSE1), a cell wall-targeted ferroxidase, and PDR2 (PHOSPHATE DEFICIENCY RESPONSE2), the single ER (endoplasmic reticulum)-resident P5-type ATPase, AtP5A, which is thought to control LPR1 secretion or activity. Autophagy is a conserved process involving the vacuolar degradation of cellular components. While the function of autophagy is well established under nutrient starvation (C, N, or S), it remains to be explored under Pi deprivation. Because AtP5A/PDR2 likely functions in the ER stress response, we analyzed the effect of Pi limitation on autophagy. Our comparative study of mutants defective in the local Pi deficiency response, ER stress response, and autophagy demonstrated that ER stress-dependent autophagy is rapidly activated as part of the developmental root response to Pi limitation and requires the genetic PDR2-LPR1 module. We conclude that Pi-dependent activation of autophagy in the root apex is a consequence of local Pi sensing and the associated ER stress response, rather than a means for systemic recycling of the macronutrient. A2 - C1 - Molecular Signal Processing ER - TY - INPR ID - 2250 TI - Capturing Evolutionary Signatures in Transcriptomes with myTAI JO - BioRxiv PY - 2016 SP - AU - Drost, H.-J. AU - Gabel, A. AU - Domazet-Lošo, T. AU - Quint, M. AU - Grosse, I. VL - UR - https://doi.org/10.1101/051565 DO - 10.1101/051565 AB - Combining transcriptome data of biological processes or response to stimuli with evolutionary information such as the phylogenetic conservation of genes or their sequence divergence rates enables the investigation of evolutionary constraints on these processes or responses. Such phylotranscriptomic analyses recently unraveled that mid-developmental transcriptomes of fly, fish, and cress were dominated by evolutionarily conserved genes and genes under negative selection and thus recapitulated the developmental hourglass on the transcriptomic level. Here, we present a protocol for performing phylotranscriptomic analyses on any biological process of interest. When applying this protocol, users are capable of detecting different evolutionary constraints acting on different stages of the biological process of interest in any species. For each step of the protocol, modular and easy-to-use open-source software tools are provided, which enable a broad range of scientists to apply phylotranscriptomic analyses to a wide spectrum of biological questions. A2 - C1 - Molecular Signal Processing ER -