Abstract

BackgroundHaloxylon ammodendron (C. A. Mey.) is widely distributed across a range of habitats, including gravel desert, clay desert, fixed and semi-fixed sand, and saline land in Asian and African deserts. To date, no genomic information or expressed sequence tag-simple sequence repeat (EST-SSR) marker has been reported for H. ammodendron plants.ResultsUsing Illumina sequencing technology, we generated over two billion bases of high-quality sequence data on H. ammodendron and conducted de novo assembly and annotation of genes without prior genome information. These reads were assembled into 79,918 unigenes (mean length = 728 bp). Based on similarity searches comparing these unigenes with known proteins in the non-redundant (nr) protein database, 25,619 unigenes were functionally annotated with a cut-off E-value of 10-5. In addition, DGE reads were mapped to the assembled transcriptome for gene expression analysis under drought stress. In total, 1,060 differentially expressed genes were identified. Among these genes, 356 genes were upregulated after drought treatment, and 704 genes were downregulated. We used the KEGG database to annotate these drought-induced genes; 207 unigenes were identified in the KEGG pathway annotation, and approximately 12.1% of the unigenes with known function fell into categories related to fatty acid metabolism, starch and sucrose metabolism, and nitrogen metabolism, suggesting that these pathways or processes may be involved in the drought response. Together, a total of 35 drought-inducible transcription factors were identified, including WRKY, MYB and bZIP family members.ConclusionsOur study is the first to provide a transcriptome sequence resource for H. ammodendron plants and to determine its digital gene expression profile under drought conditions using the assembled transcriptome data for reference. These data provide a valuable resource for genetic and genomic studies of desert plants under abiotic conditions.Electronic supplementary materialThe online version of this article (doi:10.1186/1471-2164-15-1111) contains supplementary material, which is available to authorized users.

Highlights

  • Illumina paired-end sequencing and de novo assembly To investigate the transcriptome of H. ammodendron under drought conditions, RNA was extracted from different tissues and sequenced using Illumina paired-end sequencing technology

  • After examining the gene annotation information available for these unigenes, it was found that information on gene function was available for three unigenes; no matches in any database were obtained for the remaining 8 unigenes. These results suggest that some drought-resistance pathway genes may work together to defend the plant from drought stress

  • Half of the genes examined were found to be drought-inducible. These results suggest that plants vary in their abilities to adapt to drought stress

Read more

Summary

Introduction

The regulatory mechanism in higher plants has been analysed by studying a number of genes responding to drought stress at the transcriptional level [1,2]. In Arabidopsis thaliana, for example, thousands of genes are thought to be involved in abiotic stress [3]. Drought stress-inducible genes have been classified into two groups: one group that directly protects plants against environmental stresses, and a second group that regulates gene expression networks and signalling in stress responses, such as in response to drought or salt stress [2]. Genetic studies have identified many transcription factors that are extensively involved in the regulatory network of drought-inducible genes [2,3], including, for example, the NAC [4], WRKY [5], and MYB families [6]

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.