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Field | Value |
Title | Isolation of differentially expressed genes from wheat cultivars Jinan 17 and Yumai 34 with good bread quality under heat stress during grain filling stage |
Names |
Li Hao
Zhang Ping-ping Zha Xiang-Dong Xianchun Xia He Zhonghu |
Date Issued | 2007 (iso8601) |
Abstract | Studies of gene expression patterns under heat stress during grain filling stage will provide important information for breeding wheat cultivars with high quality. In the present study, two wheat cultivars, Jinan 17 and Yumai 34 with different quality stability under various environments, were used to in the influence of high temperature on gene expression. The wheat plants were exposed to high temperature (38 °C/25 °C day/night) for three days in the middle (from 15 to 18 days post-anthesis) and late stage (from 30 to 33 days post-anthesis) of grain filling in a climate chamber. Spikelets in middle of heads were harvested, and RNA of kernels was extracted with a combined technique of cold phenolic and Trizol single-step methods. cDNA was obtained by the reverse transcription of total RNA, and differential bands were detected subsequently in cDNA-AFLP analysis. In total, 410 and 316 differential bands were detected from Jinan 17 and Yumai 34, respectively. The differential fragments were cloned, sequenced and blasted in NCBI, and 85 and 99 positive fragments of differentially expressed genes under heat stress were obtained from Jinan 17 and Yumai 34, respectively. After the positive fragments were validated by reverse Northern blotting, 25 positive fragments isolated from Jinan 17 showed intense signal, and 22 of them were induced under heat stress, which were notablely homologous to stress response genes and heat shock protein of wheat. MEanwhile, 31 positive fragments showed intense signals were observed from Yumai 34, and 25 of them were suppressed, which were notablely homologous to stress response genes, ethylene forming enzyme, pyrroline-5-carboxylate synthetase. The results indicated that gene expression was more induced under heat stress in Jinan17, whereas suppressed more in Yumai 34, which right lead to differences in heat tolerance and quality stability. Five fragments from Jinan 17, and two fragments from Yumai 34 did not have any homology sequences in the BLAST analysis, while other fragments have homology protein or nucleic acid sequences in wheat or other crops. Two fragments induces in responde to heat stress were notablely homologous to the storage protein genes, which might induce the expression of transcripts related to storage protein under hat stress. Fifteen differential fragments were detected from medium stage of grain filling in Jinan 17, whereas those from late stage were 10, while 29 and 2 differential fragments in Yumai 34 were observed in medium stage than in late stage of grain filling, specially in Yumai 34. The difference of gene expression patterns between two wheat cultivars were observed, stress response genes were induced in Jinan 17, ehylene forming enzyme and pyrroline-5-carboxylate synthetase as well as stress response genes were suppressed in Yumai 34, which may result in the different responses in heat tolerance and quality stability. The identification and characterization of wheat stress responsive genes in wheat may provide a molecular biological understanding of gene expression patterns and regulation involves in the heat stress in wheat. |
Genre | Article |
Access Condition | Open Access |
Identifier | 0496-3490 |