Abstract

Sub-zero temperatures pose a major threat to the survival of cold-climate perennials. Some of these freeze-tolerant plants produce ice-binding proteins (IBPs) that offer frost protection by restricting ice crystal growth and preventing expansion-induced lysis of the plasma membranes. Despite the extensive in vitro characterization of such proteins, the importance of IBPs in the freezing stress response has not been investigated. Using the freeze-tolerant grass and model crop, Brachypodium distachyon, we characterized putative IBPs (BdIRIs) and generated the first ‘IBP-knockdowns’. Seven IBP sequences were identified and expressed in Escherichia coli, with all of the recombinant proteins demonstrating moderate to high levels of ice-recrystallization inhibition (IRI) activity, low levels of thermal hysteresis (TH) activity (0.03−0.09°C at 1 mg/mL) and apparent adsorption to ice primary prism planes. Following plant cold acclimation, IBPs purified from wild-type B. distachyon cell lysates similarly showed high levels of IRI activity, hexagonal ice-shaping, and low levels of TH activity (0.15°C at 0.5 mg/mL total protein). The transfer of a microRNA construct to wild-type plants resulted in the attenuation of IBP activity. The resulting knockdown mutant plants had reduced ability to restrict ice-crystal growth and a 63% reduction in TH activity. Additionally, all transgenic lines were significantly more vulnerable to electrolyte leakage after freezing to −10°C, showing a 13−22% increase in released ions compared to wild-type. IBP-knockdown lines also demonstrated a significant decrease in viability following freezing to −8°C, with some lines showing only two-thirds the survival seen in control lines. These results underscore the vital role IBPs play in the development of a freeze-tolerant phenotype and suggests that expression of these proteins in frost-susceptible plants could be valuable for the production of more winter-hardy crops.

Highlights

  • Low temperatures pose a major threat to the survival of overwintering plants

  • Changes in gene expression can result in the upregulation of a number of highly-specialized proteins including cold-regulated (COR) proteins [1], cold-shock domain (CSD) proteins [4], and ice recrystallization inhibition proteins (IRIPs) [5], which are known as antifreeze proteins (AFPs) and ice-binding proteins (IBPs)

  • Putative BdIRI proteins were identified through a BLAST search using the amino acid sequence corresponding to the LpAFP gene sequence

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Summary

Introduction

Uncontrolled growth of ice crystals in the apoplast presumably sequesters water from intracellular compartments leading to cellular dehydration, loss of cell membrane integrity, physical rupture of plasma membranes and death [1]. Ice-Binding Protein Knockdown in Brachypodium distachyon withstand freezing and prevent this cascade of damage. Such plants are termed “freeze-tolerant” and have a number of biochemical, metabolic and physiological mechanisms that help prevent cell death at sub-zero temperatures. Changes in gene expression can result in the upregulation of a number of highly-specialized proteins including cold-regulated (COR) proteins [1], cold-shock domain (CSD) proteins [4], and ice recrystallization inhibition proteins (IRIPs) [5], which are known as antifreeze proteins (AFPs) and ice-binding proteins (IBPs)

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