Suberin is a fundamental plant biopolymer, found in protective tissues, such as seed coats, exodermis and endodermis of roots, the outer layers of stems and roots with secondary growth, as well as in wound-induced tissues. Its presence allows organs to resist various environmental stresses, such as pathogen attack, drought or excessive salt concentrations. Suberin is a mostly aliphatic polyester of long-chain fatty acids and alcohols, often co-occurring with lignin-like polymers in the same cells. Most suberizing cells appear to deposit suberin in the form of lamellae just outside of the plasma membrane, below the primary cell wall. The monomeric precursors of suberin are thought to be glycerated fatty acids, synthesized at the endoplasmic reticulum. However, it has remained obscure how these monomers are transported outside of the cell, where they will be polymerized to form suberin lamellae. Here, we demonstrate that extracellular vesicular-tubular structures accumulate specifically in suberizing cells. By employing various, independent mutational and hormonal challenges, known to affect suberization in distinct ways, we demonstrate that their presence correlates perfectly with root suberization. Surprisingly, no endosomal compartment marker showed any conspicuous changes upon induction of suberization, suggesting that this compartment might not derive from endosomal multi-vesicular bodies, but possibly form directly from endoplasmic reticulum subdomains. Consistent with this, we could block formation of both, suberin deposition and vesicle accumulation by a pharmacogenetic manipulation affecting early steps in the secretory pathway. Whereas many previous reports have described extracellular vesicle occurrence in the context of biotic interactions, our results suggest a developmental role for extracellular vesicles in suberin formation.
26Production of reactive-oxygen species (ROS) by NADPH oxidases (NOXs) impacts many 27 processes in animals and plants and many plant receptor pathways involve rapid, NOX-dependent 28 increases of ROS. Yet, their general reactivity has made it challenging to pinpoint the precise role 29 and direct cellular targets of ROS. A well-understood ROS target in plants are lignin peroxidases 30 in the cell wall. Lignin can be deposited with exquisite spatial control, but the underlying 31 mechanisms have remained elusive. Here we establish a full kinase signaling relay that exerts 32 direct, spatial control over ROS production and lignification within the cell wall. We show that 33 polar localization of a single kinase component is crucial for pathway function. Our data indicates 34 that an intersection of more broadly localized components allows for micrometer-scale precision 35 of lignification and that this system is triggered through initiation of ROS production as a critical 36 peroxidase co-substrate. 37 As in animals, NADPH oxidase-produced ROS in plants is important for a multitude of 38 processes and the number of NADPH oxidase genes (10 in Arabidopsis, called RESPIRATORY 39 BURST OXIDASE HOMOLOGs, RBOHs, A-J) suggests a high complexity of regulation of ROS 40 production in plants. Among its many roles, ROS-dependent regulation of plant cell wall structure and 41 function is considered to be among its most critical 1 . The cell wall is the nano-structured, sugar-based, 42 2 pressure-resisting extracellular matrix of plants and NOXs are thought to be the predominant ROS 43 source in this compartment (also termed apoplast) 1 . 44A staggering number of kinases have been shown to regulate plant NOXs and the activation 45 mechanism of NOX-dependent ROS production is well established, especially in response to microbial 46 pattern-recognition by immune receptors 2 . However, the specific role and direct molecular targets of 47 ROS during microbial pattern-recognition have remained elusive 3 . The same applies for the central 48 role of ROS in tip growing cells, such as root hairs or pollen tubes, where ROS is thought to be part of 49 an intricate oscillation of cell wall stiffening and loosening, aimed at allowing cell wall expansion 50 without catastrophic collapse 4,5 . In this case, ROS is proposed to be important for counteracting cell 51 wall loosening pH decreases, but it is again unclear what direct targets of ROS would mediate cell wall 52 stiffening. Cell wall lignification by apoplastic peroxidases, can therefore be considered as the most 53 well-established role of ROS, where the peroxidases themselves are the direct "ROS targets", using it 54 as a co-substrate for the oxidation of mono-lignols 6,7 . In the case of lignification, however, a 55 molecularly-defined signaling pathway that induces ROS production during lignification has not been 56 defined. A few years ago, our group identified a specific NADPH oxidase, RBOHF, to be required for 57 the localized formation of lignin in the root end...
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