Plant Biology Laboratory, The Salk Institute for Biological Studies, La Jolla, United States
Adi Yaaran
The Robert H. Smith Institute of Plant Sciences and Genetics in Agriculture, Faculty of Agriculture, Food, and Environment, The Hebrew University of Jerusalem, Rehovot, Israel
Jiaying Xu
Plant Biology Laboratory, The Salk Institute for Biological Studies, La Jolla, United States
Charlotte Miller
Plant Biology Laboratory, The Salk Institute for Biological Studies, La Jolla, United States
Natanella Illouz-Eliaz
Plant Biology Laboratory, The Salk Institute for Biological Studies, La Jolla, United States
Joseph R Nery
Genomic Analysis Laboratory, The Salk Institute for Biological Studies, La Jolla, United States
Wolfgang Busch
Plant Biology Laboratory, The Salk Institute for Biological Studies, La Jolla, United States
Yotam Zait
The Robert H. Smith Institute of Plant Sciences and Genetics in Agriculture, Faculty of Agriculture, Food, and Environment, The Hebrew University of Jerusalem, Rehovot, Israel
Plant Biology Laboratory, The Salk Institute for Biological Studies, La Jolla, United States; Genomic Analysis Laboratory, The Salk Institute for Biological Studies, La Jolla, United States; Howard Hughes Medical Institute, The Salk Institute for Biological Studies, La Jolla, United States
Soil-free assays that induce water stress are routinely used to investigate drought responses in the plant Arabidopsis thaliana. Due to their ease of use, the research community often relies on polyethylene glycol (PEG), mannitol, and salt (NaCl) treatments to reduce the water potential of agar media, and thus induce drought conditions in the laboratory. However, while these types of stress can create phenotypes that resemble those of water deficit experienced by soil-grown plants, it remains unclear how these treatments compare at the transcriptional level. Here, we demonstrate that these different methods of lowering water potential elicit both shared and distinct transcriptional responses in Arabidopsis shoot and root tissue. When we compared these transcriptional responses to those found in Arabidopsis roots subject to vermiculite drying, we discovered many genes induced by vermiculite drying were repressed by low water potential treatments on agar plates (and vice versa). Additionally, we also tested another method for lowering water potential of agar media. By increasing the nutrient content and tensile strength of agar, we show the ‘hard agar’ (HA) treatment can be leveraged as a high-throughput assay to investigate natural variation in Arabidopsis growth responses to low water potential.