4.7 Article

Arabidopsis thaliana EARLY RESPONSIVE TO DEHYDRATION 7 Localizes to Lipid Droplets via Its Senescence Domain

Journal

FRONTIERS IN PLANT SCIENCE
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fpls.2021.658961

Keywords

EARLY RESPONSIVE TO DEHYDRATION 7; lipid droplet; plant lipids; senescence domain; senescence domain-containing protein; senescence; spartin-associated domain; spartin; stress

Categories

Funding

  1. US Department of Energy, Office of Science, BES-Physical Biosciences program [DE-SC0016536]
  2. Natural Sciences and Engineering Research Council of Canada [RGPIN-2018-04629]
  3. Deutsche Forschungsgemeinschaft [IS 273/2-2, DFG-GZ: INST 186/1230-1 FUGG]
  4. U.S. Department of Energy (DOE) [DE-SC0016536] Funding Source: U.S. Department of Energy (DOE)

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Lipid droplets (LDs) are neutral-lipid-containing organelles found in all kingdoms of life and coated with proteins that carry out various functions; ERD7, identified as a putative LD protein in plants, may be involved in stress responses and localized to the surface of LDs.
Lipid droplets (LDs) are neutral-lipid-containing organelles found in all kingdoms of life and are coated with proteins that carry out a vast array of functions. Compared to mammals and yeast, relatively few LD proteins have been identified in plants, particularly those associated with LDs in vegetative (non-seed) cell types. Thus, to better understand the cellular roles of LDs in plants, a more comprehensive inventory and characterization of LD proteins is required. Here, we performed a proteomics analysis of LDs isolated from drought-stressed Arabidopsis leaves and identified EARLY RESPONSIVE TO DEHYDRATION 7 (ERD7) as a putative LD protein. mCherry-tagged ERD7 localized to both LDs and the cytosol when ectopically expressed in plant cells, and the protein's C-terminal senescence domain (SD) was both necessary and sufficient for LD targeting. Phylogenetic analysis revealed that ERD7 belongs to a six-member family in Arabidopsis that, along with homologs in other plant species, is separated into two distinct subfamilies. Notably, the SDs of proteins from each subfamily conferred targeting to either LDs or mitochondria. Further, the SD from the ERD7 homolog in humans, spartin, localized to LDs in plant cells, similar to its localization in mammals; although, in mammalian cells, spartin also conditionally localizes to other subcellular compartments, including mitochondria. Disruption of ERD7 gene expression in Arabidopsis revealed no obvious changes in LD numbers or morphology under normal growth conditions, although this does not preclude a role for ERD7 in stress-induced LD dynamics. Consistent with this possibility, a yeast two-hybrid screen using ERD7 as bait identified numerous proteins involved in stress responses, including some that have been identified in other LD proteomes. Collectively, these observations provide new insight to ERD7 and the SD-containing family of proteins in plants and suggest that ERD7 may be involved in functional aspects of plant stress response that also include localization to the LD surface.

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