Abstract

MicroRNAs (miRNA) families act as critical regulators for plant growth, development, and responses to abiotic stresses. In this study, we characterized TaemiR408, a miRNA family member of wheat (Triticum aestivum), for the role in mediating plant responses to Pi starvation and salt stress. TaemiR408 targets six genes that encode proteins involving biochemical metabolism, microtubule organization, and signaling transduction. 5′- and 3′-RACE analyses confirmed the mRNA cleavage of target genes mediated by this wheat miRNA. TaemiR408 showed induced expression patterns upon Pi starvation and salt stress and whose upregulated expression was gradually repressed by the normal recovery treatments. The target genes of TaemiR408 exhibited reverse expression patterns to this miRNA, whose transcripts were downregulated under Pi starvation and salt stress and the reduced expression was recovered by the followed normal condition. These results suggest the regulation of the target genes under TaemiR408 through a cleavage mechanism. Tobacco lines with TaemiR408 overexpression exhibited enhanced stress tolerance, showing improved phenotype, biomass, and photosynthesis behavior compared with wild type under both Pi starvation and salt treatments, which closely associate increased P accumulation upon Pi deprivation and elevated osmolytes under salt stress, respectively. Phosphate transporter (PT) gene NtPT2 displays upregulated transcripts in the Pi-deprived TaemiR408 overexpressors; knockdown of this PT gene reduces Pi acquisition under low-Pi stress, confirming its role in improving plant Pi taken up. Likewise, NtPYL2 and NtSAPK3, genes encoding abscisic acid (ABA) receptor and SnRK2 protein, respectively, exhibited upregulated transcripts in salt-challenged TaemiR408 overexpressors; knockdown of them caused deteriorated growth and lowered osmolytes amounts of plants upon salt treatment. Thus, TaemiR408 is crucial for plant adaptations to Pi starvation and salt stress through regulating Pi acquisition under low-Pi stress and remodel ABA signaling pathway and osmoprotects biosynthesis under salt stress.

Highlights

  • Phosphorus (P) deficiency and salt stress are two of the pronouncing abiotic stresses negatively regulating plant growth, development, and crop productivity

  • Our amplified NtMIR408 is not same as the miR408 member deposited in N. tabacum miRNA database (Accession No MI0021410), suggesting that miR408 is conserved and the tobacco miR408 family consists of a set of members

  • A growing body of evidence has confirmed the critical role of miRNA-guided gene regulation in mediating plant response to diverse abiotic stresses, including Pi starvation and high salinity

Read more

Summary

Introduction

Phosphorus (P) deficiency and salt stress are two of the pronouncing abiotic stresses negatively regulating plant growth, development, and crop productivity. A line of evidence has suggested that plants cope with Pi starvation to sometimes crosstalk with the salt stress tolerance (Baek et al, 2016). To cope with low-Pi stress, plants have evolved a variety of adaptive mechanisms, such as modulation of root system architecture (RSA) establishment, enhancement of Pi acquisition activity, and elevation of secretion of organic acids and phosphatases (Raghothama, 1999; Poirier and Bucher, 2002; Yuan and Liu, 2008; Péret et al, 2011). Plants have established a subset of pathways to withstand salt stress, through regulating osmolyte biosynthesis, stomota movement, cellular structure, and developmental plasticity via an abscisic acid (ABA)-dependent cascade (Giraudat, 1995; Zhu, 2002; Raghavendra et al, 2010). Further elucidating the molecular mechanisms underlying plant responses to Pi starvation and salt stress are helpful in engineering crop cultivars with improved tolerance to these adverse stressors

Methods
Results
Conclusion

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.