Comparative analysis of ESTs in response to drought stress in chickpea (C. arietinum L.)

被引:43
作者
Gao, Wen-Rui [2 ]
Wang, Xian-Sheng [2 ]
Liu, Qing-You [1 ]
Peng, Hui [2 ]
Chen, Chen [2 ]
Li, Jian-Gui [3 ]
Zhang, Ju-Song [3 ]
Hu, Song-Nian [1 ]
Ma, Hao [2 ]
机构
[1] Chinese Acad Sci, Beijing Inst Genom, Beijing 100029, Peoples R China
[2] Nanjing Agr Univ, Dept Agr, Natl Ctr Soybean Improvement, State Key Lab Crop Genet & Germplasm Enhancement, Nanjing 210095, Peoples R China
[3] Xinjiang Agr Univ, Key Lab Agr Biotechnol, Urumqi 830052, Xinjiang Uygur, Peoples R China
基金
中国国家自然科学基金;
关键词
Chickpea; Drought stress; Drought tolerance; cDNA library; Expressed sequence tags; Quantitative real-time PCR;
D O I
10.1016/j.bbrc.2008.09.030
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chickpea (Cicer arietinum L.) is an important pulse crop grown mainly in the arid and semi-arid regions. To identify the water-stress-induced genes, two non-normalized cDNA libraries were constructed from the seedling leaves of a drought-tolerant chickpea cultivar under PEG-treated and -nontreated conditions. About 2500 clones from each library were selected randomly for sequencing analysis. Based on IDEG6 online software analysis, 92 genes were differentially expressed, and these genes were involved in diverse biological progresses, Such as Metabolism, transcription, signal transduction, protein Synthesis and others. Most of the up-regulated genes were related to drought tolerance, and the down-regulated genes were mainly involved in photosynthesis. The differential expression patterns of five functional unigenes were confirmed by quantitative real-time PCR (qPCR). The results Will help in understanding the molecular basis Of drought tolerance in chickpea. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:578 / 583
页数:6
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