Abstract

The early light-induced proteins (ELIPs) are postulated to act as transient pigment-binding proteins that protect the chloroplast from photodamage caused by excessive light energy. Desert mosses such as Syntrichia caninervis, that are desiccation-tolerant and homoiochlorophyllous, are often exposed to high-light conditions when both hydrated and dry ELIP transcripts are accumulated in response to dehydration. To gain further insights into ELIP gene function in the moss S. caninervis, two ELIP cDNAs cloned from S. caninervis, ScELIP1 and ScELIP2 and both sequences were used as the basis of a transcript abundance assessment in plants exposed to high-light, UV-A, UV-B, red-light, and blue-light. ScELIPs were expressed separately in an Arabidopsis ELIP mutant Atelip. Transcript abundance for ScELIPs in gametophytes respond to each of the light treatments, in similar but not in identical ways. Ectopic expression of either ScELIPs protected PSII against photoinhibition and stabilized leaf chlorophyll content and thus partially complementing the loss of AtELIP2. Ectopic expression of ScELIPs also complements the germination phenotype of the mutant and improves protection of the photosynthetic apparatus of transgenic Arabidopsis from high-light stress. Our study extends knowledge of bryophyte photoprotection and provides further insight into the molecular mechanisms related to the function of ELIPs.

Highlights

  • Light is an essential energy source for all plant life and is used to generate a usable carbon-based energy source for growth via photosynthesis, when light intensities exceed the plant’s saturated photosynthesis requirements it has the potential to cause damage to the plant [1]

  • Expression of ScELIPs in the Atelip mutant increase germination rates but the rates do not attain WT rates when grown in red, blue, Ultraviolet B (UVB), and high-light conditions

  • In S. caninervis, ScELIP1 transcripts declined in abundance in response to Ultraviolet A (UVA) and ScELIP2 transcript levels only exhibited a response to UVA after a 4 h exposure (Figure 2a)

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Summary

Introduction

Light is an essential energy source for all plant life and is used to generate a usable carbon-based energy source for growth via photosynthesis, when light intensities exceed the plant’s saturated photosynthesis requirements it has the potential to cause damage to the plant [1]. This potential damage is driven by an overproduction of reactive oxygen species (ROS). Photoinhibition in turn results in the degradation of carotenoids, bleaching of chlorophylls, and an increase in lipid peroxidation driven by the reactive-oxygen derivatives [4]. Photosynthetic organisms must find a balance between the requirements for efficient light harvesting and the danger of accumulating light-induced damage when light absorption exceeds the photosynthesis capacity

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