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In plant cells, environmental stressors induce changes in the cytosolic concentration of calcium ([Ca 2+ ] cyt ) that are transduced by Ca 2+ -sensing proteins. To confer specificity to the stress signaling response, [Ca 2+ ] cyt sensing must be tightly regulated in space and time; the molecular mechanisms that restrict the localization and dynamics of Ca 2+ sensors in plants, however, are largely unknown. In this report, we identify a putative Ca 2+ -sensitive complex containing the synaptotagmins 1 and 5 (SYT1 and SYT5) and the Ca 2+ -dependent lipid binding protein (CLB1), which is enriched at ER-PM contact sites (EPCS) and relocalizes in response to Rare Earth Elements (REEs)-induced endocytosis. Our results show that endocytosed REEs influence cytosolic Ca 2+ signaling, as indicated by the activation of the Ca 2+ /Calmodulin-based ratiometric sensor GCaMP3, and promote the cytoskeleton-dependent accumulation of ER-PM contact sites at the cell cortex. Based on these results, we propose that the EPCS-localized SYT1/SYT5/CLB1 complex is part of an evolutionarily conserved and spatially regulated Ca 2+ -responsive mechanism that control cER-PM communication during stress episodes.
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Lee et al. (2019) studied this question.