Abstract

Salt and drought stress severely reduce plant growth and crop productivity worldwide. The identification of genes underlying stress response and tolerance is the subject of intense research in plant biology. Through microarray analyses, we previously identified in potato (Solanum tuberosum) StRGGA, coding for an Arginine Glycine Glycine (RGG) box-containing RNA-binding protein, whose expression was specifically induced in potato cell cultures gradually exposed to osmotic stress. Here, we show that the Arabidopsis (Arabidopsis thaliana) ortholog, AtRGGA, is a functional RNA-binding protein required for a proper response to osmotic stress. AtRGGA gene expression was up-regulated in seedlings after long-term exposure to abscisic acid (ABA) and polyethylene glycol, while treatments with NaCl resulted in AtRGGA down-regulation. AtRGGA promoter analysis showed activity in several tissues, including stomata, the organs controlling transpiration. Fusion of AtRGGA with yellow fluorescent protein indicated that AtRGGA is localized in the cytoplasm and the cytoplasmic perinuclear region. In addition, the rgga knockout mutant was hypersensitive to ABA in root growth and survival tests and to salt stress during germination and at the vegetative stage. AtRGGA-overexpressing plants showed higher tolerance to ABA and salt stress on plates and in soil, accumulating lower levels of proline when exposed to drought stress. Finally, a global analysis of gene expression revealed extensive alterations in the transcriptome under salt stress, including several genes such as ASCORBATE PEROXIDASE2, GLUTATHIONE S-TRANSFERASE TAU9, and several SMALL AUXIN UPREGULATED RNA-like genes showing opposite expression behavior in transgenic and knockout plants. Taken together, our results reveal an important role of AtRGGA in the mechanisms of plant response and adaptation to stress.

Highlights

  • Bacillus anthracis is an encapsulated, endospore-forming, gram-positive rod and is the causative agent of anthrax [1, 8]

  • Mice were immunized with formalin-fixed encapsulated B. anthracis bacilli, and the serum antibody response to a ␥-D-glutamyl capsular epitope was measured

  • Polysaccharides are the prototypic example of TI-2 antigens, proteins containing repeating antigenic determinants, viruses, and synthetic amino acid polymers may function as TI-2 antigens [9, 12, 13]

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Summary

Introduction

Bacillus anthracis is an encapsulated, endospore-forming, gram-positive rod and is the causative agent of anthrax [1, 8]. Mice were immunized with formalin-fixed encapsulated B. anthracis bacilli, and the serum antibody response to a ␥-D-glutamyl capsular epitope was measured. These response patterns define the capsule of B. anthracis as a thymus-independent type 2 antigen.

Results
Conclusion
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