Abstract

BackgroundFlavonoids can protect plants against extreme temperatures and ROS due to their antioxidant activities. We found that deep-purple seed coat color was controlled by two gene interaction (12:3:1) from the cross between yellow and deep-purple seed coat colored inbreds. F2:3 seeds were grouped in 3 by seed coat color and germinated under chilling (4 °C) and non-acclimated conditions (18 °C) for a week, followed by normal conditions (18 °C) for three weeks and a subsequent chilling stress (4 °C) induction. We analyzed mean daily germination in each group. Additionally, to study the acclimation in relationship to the different seed coat colors on the germination ability and seedling performances under the cold temperatures, we measured the chlorophyll content, ROS scavenging activity, and expression levels of genes involved in ROS scavenging, flavonoid biosynthetic pathway, and cold response in seedlings.ResultsThe results of seed color segregation between yellow and deep purple suggested a two-gene model. In the germination study, normal environmental conditions induced the germination of yellow-seed, while under chilling conditions, the germination ratio of deep purple-seed was higher than that of yellow-colored seeds. We also found that the darker seed coat colors were highly responsive to cold acclimation based on the ROS scavenging enzymes activity and gene expression of ROS scavenging enzymes, flavonoid biosynthetic pathway and cold responsive genes.ConclusionsWe suggest that deep purple colored seed might be in a state of innate pre-acquired stress response state under normal conditions to counteract stresses in a more effective way. Whereas, after the acclimation, another stress should enhance the cold genes expression response, which might result in a more efficient chilling stress response in deep purple seed seedlings.Low temperature has a large impact on the yield of crops. Thus, understanding the benefit of seed coat color response to chilling stress and the identification of limiting factors are useful for developing breeding strategies in order to improve the yield of wheat under chilling stress.

Highlights

  • Flavonoids can protect plants against extreme temperatures and reactive oxygen species (ROS) due to their antioxidant activities

  • Understanding the benefit of seed coat color response to chilling stress and the identification of limiting factors are useful for developing breeding strategies in order to improve the yield of wheat under chilling stress

  • This work aimed to evaluate the effects of chilling stress in different seed coat colors under non- acclimated and chilling-acclimated seeds and seedlings were evaluated in chlorophyll content, enzymatic activity, and gene expression of flavonoid related pathway, ROS scavenging enzyme genes and cold responsive genes in order to better characterize the seed coat color response to chilling stress and identify limiting factors useful for developing breeding strategies in order to improve the yield of wheat under chilling stress

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Summary

Introduction

Flavonoids can protect plants against extreme temperatures and ROS due to their antioxidant activities. ­F2:3 seeds were grouped in 3 by seed coat color and germinated under chilling (4 °C) and non-acclimated conditions (18 °C) for a week, followed by normal conditions (18 °C) for three weeks and a subsequent chilling stress (4 °C) induction. To study the acclimation in relationship to the different seed coat colors on the germination ability and seedling performances under the cold temperatures, we measured the chlorophyll content, ROS scavenging activity, and expression levels of genes involved in ROS scavenging, flavonoid biosynthetic pathway, and cold response in seedlings. The increasing population and climate change are challenges for future agriculture production. Previous studies have reported that chilling temperatures can inhibit phloem export [7,8,9,10], decrease carbon fixation [7], interrupt the circadian rhythm by regulating the transcription of photosynthetic genes [11], and degrade damaged reaction PSII centers [12]

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