Abstract

Heat Shock Factor A2 (HsfA2) is part of the Heat Shock Factor (HSF) network, and plays an essential role beyond heat shock in environmental stress responses and cellular homeostatic control. Arabidopsis thaliana cell cultures derived from wild type (WT) ecotype Col-0 and a knockout line deficient in the gene encoding HSFA2 (HSFA2 KO) were grown aboard the International Space Station (ISS) to ascertain whether the HSF network functions in the adaptation to the novel environment of spaceflight. Microarray gene expression data were analyzed using a two-part comparative approach. First, genes differentially expressed between the two environments (spaceflight to ground) were identified within the same genotype, which represented physiological adaptation to spaceflight. Second, gene expression profiles were compared between the two genotypes (HSFA2 KO to WT) within the same environment, which defined genes uniquely required by each genotype on the ground and in spaceflight-adapted states. Results showed that the endoplasmic reticulum (ER) stress and unfolded protein response (UPR) define the HSFA2 KO cells’ physiological state irrespective of the environment, and likely resulted from a deficiency in the chaperone-mediated protein folding machinery in the mutant. Results further suggested that additional to its universal stress response role, HsfA2 also has specific roles in the physiological adaptation to spaceflight through cell wall remodeling, signal perception and transduction, and starch biosynthesis. Disabling HsfA2 altered the physiological state of the cells, and impacted the mechanisms induced to adapt to spaceflight, and identified HsfA2-dependent genes that are important to the adaption of wild type cells to spaceflight. Collectively these data indicate a non-thermal role for the HSF network in spaceflight adaptation.

Highlights

  • Survival in a challenging environment requires a coordinated system that enables a living organism to respond appropriately to a change

  • In a spaceflight horizontal comparison, the gene expression in HSFA2 KO cells in spaceflight was compared to gene expression in wild type (WT) cells in spaceflight, defining unique genes required for the spaceflight adapted state in each genotype

  • Undifferentiated Arabidopsis thaliana cell cultures were flown to the International Space Station (ISS) as part of the Biological Research In Cannisters 17 (BRIC17) Cellular Expression Logic (CEL) experiment to enhance the understanding of how cells lacking HSFA2, a key transcription factor involved in the response to terrestrial stress stimuli, physiologically adapt to the novel environment of spaceflight

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Summary

Introduction

Survival in a challenging environment requires a coordinated system that enables a living organism to respond appropriately to a change. The environment of the International Space Station (ISS) presents novel challenges for all terrestrial organisms, which evolved in the unit gravity of Earth. When terrestrial organisms are transported to the ISS, they respond by adjusting metabolic processes to physiologically adapt to this new spaceflight environment. One readout of the physiological changes induced by spaceflight is in the patterns of gene expression. Individual genes have been implicated as important to the altered gravity physiological adaptation through assays with deletion mutants [1,2] and with specific assays of expression [3,4,5,6,7]. Genome-wide evaluations have provided a large-scale view of the changes elicited by disrupted terrestrial gravity environments [8,9,10,11]

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