Upon stress, a trade-off between plant growth and defense responses defines the capacity for survival. Stress can result in accumulation of misfolded proteins in the endoplasmic reticulum (ER) and other organelles. To cope with these proteotoxic effects, plants rely on the unfolded protein response (UPR). The involvement of reactive oxygen species (ROS), ethylene (ETH), and sugars, as well as their crosstalk, in general stress responses is well established, yet their role in UPR deserves further scrutiny. Here, a synopsis of current evidence for ROS-ETH-sugar crosstalk in UPR is discussed. We propose that this triad acts as a major signaling hub at the crossroads of survival and death, integrating information from ER, chloroplasts, and mitochondria, thereby facilitating a coordinated stress response.
Coordinated Inter-Organelle Stress Responses Facilitate Plant SurvivalThe sessile nature of plants implies that they are inherently subject to changing environments. As such, they need to cope with a variety of (a)biotic stresses. These harmful conditions lead to a set of shared but also distinct responses that can include oxidative stress (see Glossary), osmotic or ionic imbalances, and changes in cellular components, all of which modify the physiological status. Growth and development are hindered under such conditions, either directly, for instance by oxidative damage of essential biomolecules, or indirectly, through reprogramming of energy metabolism. In particular, the functioning of chloroplasts and mitochondria, the 'powerhouses' of the cell, is disturbed upon stress. The associated changes in carbohydrate status and ultimately energy levels, affect growth, but probably also serve as important stress signals (Figure 1, Key Figure) [1]. As such, mitochondria and chloroplasts act as central hubs that integrate external and internal signals to coordinate growth [2-4].Importantly, stress perception and its downstream responses should be considered as contextdependent, and are influenced by the stress type, severity, and duration. Nevertheless, an integral aspect of stress is the accumulation of unfolded or misfolded proteins (i.e., proteotoxic stress) [5]. The ER is essential for protein folding and secretion and has different mechanisms for protein quality control (QC). However, once the amount of unfolded or misfolded proteins surpasses the level that can be controlled by the ERQC, cells have to cope with the cytotoxicity of hampered proteostasis, called ER stress. This also occurs in chloroplasts and mitochondria [6,7]. Restoration of organellar proteostasis requires responses from both the organelle and the nucleus, and depends on intricate crosstalk between subcellular compartments. Hence, a tight communication established via anterograde and retrograde signaling is necessary for coordinated gene expression to restore proteostasis (Box 1). Eukaryotes rely on the evolutionary conserved retrograde signaling pathway called the UPR, that initiates a series of transcriptional Highlights Proteotoxic stress, or the ...