Abstract

Soil destruction by abiotic environmental conditions, such as high salinity, has resulted in dramatic losses of arable land, giving rise to the need of studying mechanisms of plant adaptation to salt stress aimed at creating salt-tolerant plants. Recently, it has been reported that cytokinins (CKs) regulate plant environmental stress responses through two-component systems. A decrease in endogenous CK levels could enhance salt and drought stress tolerance. Here, we have investigated the global transcriptional change caused by a reduction in endogenous CK content under both normal and salt stress conditions. Ten-day-old Arabidopsis thaliana wild-type (WT) and CK-deficient ipt1,3,5,7 plants were transferred to agar plates containing either 0 mM (control) or 200 mM NaCl and maintained at normal growth conditions for 24 h. Our experimental design allowed us to compare transcriptome changes under four conditions: WT-200 mM vs. WT-0 mM, ipt1,3,5,7-0 mM vs. WT-0 mM, ipt1,3,5,7-200 mM vs. ipt1,3,5,7-0 mM and ipt1,3,5,7-200 mM vs. WT-200 mM NaCl. Our results indicated that the expression of more than 10% of all of the annotated Arabidopsis genes was altered by CK deficiency under either normal or salt stress conditions when compared to WT. We found that upregulated expression of many genes encoding either regulatory proteins, such as NAC, DREB and ZFHD transcription factors and the calcium sensor SOS3, or functional proteins, such as late embryogenesis-abundant proteins, xyloglucan endo-transglycosylases, glycosyltransferases, glycoside hydrolases, defensins and glyoxalase I family proteins, may contribute to improved salt tolerance of CK-deficient plants. We also demonstrated that the downregulation of photosynthesis-related genes and the upregulation of several NAC genes may cause the altered morphological phenotype of CK-deficient plants. This study highlights the impact of CK regulation on the well-known stress-responsive signaling pathways, which regulate plant adaptation to high salinity as well as other environmental stresses.

Highlights

  • Salt stress is one of the major abiotic stresses experienced by plants worldwide, affecting approximately 7% of the world’s total land area [1,2]

  • Our results suggest that reduction of bioactive CK levels induced changes in gene expression of many regulatory and functional genes, including transcription factors (TFs), calcium sensors, high affinity K+/Na+ co-transporter proteins, heat shock proteins, late embryogenesis-abundant (LEA) proteins, xyloglucan endo-transglycosylases (XTR), glycosyltransferases (GTs), glycoside hydrolases (GHs), defensins and glyoxalase I family proteins, leading to improved salt and drought stress tolerance of the ipt1,3,5,7 mutant

  • Plant materials and salt stress treatment WT Arabidopsis (Columbia ecotype) and CK-deficient ipt1,3,5,7 (Columbia ecotype) seeds [21] were sowed on germination medium (GM) agar plates supplemented with 3% sucrose and kept for 4 days at 4uC

Read more

Summary

Introduction

Salt stress is one of the major abiotic stresses experienced by plants worldwide, affecting approximately 7% of the world’s total land area [1,2]. Mild salt stress primarily affects plant development, agronomy traits and agricultural productivity, but extremely high salinity stress can lead to plant death. Climate change and declining water quality are of great concern because they contribute to land degradation by causing high salinity levels in soil. To cope with salinity stress, plants employs various mechanisms, at both the whole plant and cellular levels, which are controlled by a variety of genes and signaling pathways and are expressed and activated at different times during the life of a plant [4,6,7]. With the availability of genomic sequences from various plant species and recent advances in microarray technologies, genes associated with high salinity tolerance have been identified on a large scale at a genome-wide level [2,10,11]. Together with other omic technologies, such as proteomics and metabolomics, transcriptomics has contributed significantly to the elucidation of stress responses [12,13,14]

Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.