Abstract

BackgroundTo compensate for the lack of information about the molecular mechanism involved in Arundo donax L. response to salt stress, we de novo sequenced, assembled and analyzed the A. donax leaf transcriptome subjected to two levels of long-term salt stress (namely, S3 severe and S4 extreme).ResultsThe picture that emerges from the identification of differentially expressed genes is consistent with a salt dose-dependent response. Hence, a deeper re-programming of the gene expression occurs in those plants grew at extreme salt level than in those subjected to severe salt stress, probably representing for them an “emergency” state. In particular, we analyzed clusters related to salt sensory and signaling, transcription factors, hormone regulation, Reactive Oxygen Species (ROS) scavenging, osmolyte biosynthesis and biomass production, all of them showing different regulation either versus untreated plants or between the two treatments. Importantly, the photosynthesis is strongly impaired in samples treated with both levels of salinity stress. However, in extreme salt conditions, a dramatic switch from C3 Calvin cycle to C4 photosynthesis is likely to occur, this probably being the more impressive finding of our work.ConclusionsConsidered the distinct response to salt doses, genes either involved in severe or in extreme salt response could constitute useful markers of the physiological status of A. donax to deepen our understanding of its biology and productivity in salinized soil. Finally, many of the unigenes identified in the present study have the potential to be used for the development of A. donax varieties with improved productivity and stress tolerance, in particular the knock out of the GTL1 gene acting as negative regulator of water use efficiency has been proposed as good target for genome editing.

Highlights

  • To compensate for the lack of information about the molecular mechanism involved in Arundo donax L. response to salt stress, we de novo sequenced, assembled and analyzed the A. donax leaf transcriptome subjected to two levels of long-term salt stress

  • The number of differentially expressed genes (DEGs) under extreme salt stress is much higher than that observed in severe salt stress suggesting that a deep re-programming of the gene expression must occur in Extreme salt stress (S4) samples, which, during the experiment, certainly grew in an “emergency” state

  • Once A. donax plants were subjected to S4 extreme salt stress a clear down regulation of abscisic acid (ABA) biosynthetic genes is registered suggesting that ABA synthesis might have a key role during the onset of stressful conditions as demonstrated in other species [63] and in the case of water stress [33] but not in the case of long term stress

Read more

Summary

Introduction

To compensate for the lack of information about the molecular mechanism involved in Arundo donax L. response to salt stress, we de novo sequenced, assembled and analyzed the A. donax leaf transcriptome subjected to two levels of long-term salt stress (namely, S3 severe and S4 extreme). Useful A. donax genomic resources were provided by the work of Sablok et al [30] which used tissue-specific NGS of four different organs (leaf, culm, bud and root) of one A. donax ecotype constituting a comprehensive reference catalog of transcripts aimed at characterizing and improving the spatial and temporal patterns of expression underlying the high productivity of biomass. Considering the frequent occurrence of soil salinity in the Mediterranean area and the potential use of marginal soil for energy crop cultivation aimed to overcome the incoming food security risks, a deep knowledge of the global transcriptomic response of giant reed to salt is needed seeing as it is not yet available. This study lays the foundation to select candidate genes for cis- and trans-genesis with the aim to develop plants with improved salt stress tolerance

Methods
Results
Discussion
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.