RNA-Seq analysis of the wild barley (H. spontaneum) leaf transcriptome under salt stress

被引:62
作者
Bahieldin, Ahmed [1 ,2 ]
Atef, Ahmed [1 ]
Sabir, Jamal S. M. [1 ]
Gadalla, Nour O. [1 ,3 ]
Edris, Sherif [1 ,2 ]
Alzohairy, Ahmed M. [4 ]
Radhwan, Nezar A. [1 ]
Baeshen, Mohammed N. [1 ]
Ramadan, Ahmed M. [1 ,5 ]
Eissa, Hala F. [5 ,6 ]
Hassan, Sabah M. [1 ,2 ]
Baeshen, Nabih A. [1 ]
Abuzinadah, Osama [1 ]
Al-Kordy, Magdy A. [1 ,3 ]
El-Domyati, Fotouh M. [1 ,2 ]
Jansen, Robert K. [1 ,7 ]
机构
[1] King Abdulaziz Univ, Fac Sci, Dept Biol Sci, POB 80141, Jeddah 21589, Saudi Arabia
[2] Ain Shams Univ, Fac Agr, Dept Genet, Cairo, Egypt
[3] Natl Res Ctr, Genet & Cytol Dept, Genet Engn & Biotechnol Div, Dokki, Egypt
[4] Zagazig Univ, Fac Agr, Dept Genet, Zagazig 44511, Egypt
[5] Agr Genet Engn Res Inst, Agr Res Ctr, Giza, Egypt
[6] MUST, Fac Biotechnol, 6th October City, Egypt
[7] Univ Texas Austin, Dept Integrat Biol, Austin, TX 78712 USA
关键词
Electron transport; Flavonoid biosynthesis; Reactive oxygen species; SERINE/THREONINE PROTEIN-KINASE; SUPEROXIDE-DISMUTASE; ISOFLAVONE REDUCTASE; SIGNAL-TRANSDUCTION; ECTOPIC EXPRESSION; CHALCONE ISOMERASE; CULTIVATED BARLEY; METAL-BINDING; ENHANCES SALT; H+-ATPASE;
D O I
10.1016/j.crvi.2015.03.010
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Wild salt-tolerant barley (Hordeum spontaneum) is the ancestor of cultivated barley (Hordeum vulgare or H. vulgare). Although the cultivated barley genome is well studied, little is known about genome structure and function of its wild ancestor. In the present study, RNA-Seq analysis was performed on young leaves of wild barley treated with salt (500 mM NaCl) at four different time intervals. Transcriptome sequencing yielded 103 to 115 million reads for all replicates of each treatment, corresponding to over 10 billion nucleotides per sample. Of the total reads, between 74.8 and 80.3% could be mapped and 77.4 to 81.7% of the transcripts were found in the H. vulgare unigene database (unigene-mapped). The unmapped wild barley reads for all treatments and replicates were assembled de novo and the resulting contigs were used as a new reference genome. This resulted in 94.3 to 953% of the unmapped reads mapping to the new reference. The number of differentially expressed transcripts was 9277, 3861 of which were unigene-mapped. The annotated unigene- and de novo-mapped transcripts (5100) were utilized to generate expression clusters across time of salt stress treatment. Two-dimensional hierarchical clustering classified differential expression profiles into nine expression clusters, four of which were selected for further analysis. Differentially expressed transcripts were assigned to the main functional categories. The most important groups were "response to external stimulus" and "electron-carrier activity". Highly expressed transcripts are involved in several biological processes, including electron transport and exchanger mechanisms, flavonoid biosynthesis, reactive oxygen species (ROS) scavenging, ethylene production, signaling network and protein refolding. The comparisons demonstrated that mRNA-Seq is an efficient method for the analysis of differentially expressed genes and biological processes under salt stress. (C) 2015 Academie des sciences. Published by Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:285 / 297
页数:13
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