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作物学报 ›› 2013, Vol. 39 ›› Issue (06): 1045-1053.doi: 10.3724/SP.J.1006.2013.01045

• 作物遗传育种·种质资源·分子遗传学 • 上一篇    下一篇

花生干旱胁迫响应基因的数字表达谱分析

孙爱清1,**,张杰道2,**,万勇善1,*,刘风珍1,张昆1,孙利1   

  1. 1 山东农业大学农学院 / 作物生物学国家重点实验室 / 山东省作物生物学重点实验室, 山东泰安 271018; 2 山东农业大学生命科学学院, 山东泰安 271018
  • 收稿日期:2012-07-06 修回日期:2013-01-15 出版日期:2013-06-12 网络出版日期:2013-02-19
  • 通讯作者: 万勇善, E-mail: yswan@sdau.edu.cn, Tel: +86 (0)538 8241540
  • 基金资助:

    本研究由国家现代农业产业技术体系建设专项资金(CARS-14-07B), 国家自然科学基金项目(31101177)和山东省自然科学基金(ZR2011CQ027)资助。

In silico Expression Profile of Genes in Response to Drought in Peanut

SUN Ai-Qing1,**,ZHANG Jie-Dao2,**,WAN Yong-Shan1,*,LIU Feng-Zhen1,ZHANG Kun1,SUN Li1   

  1. 1 State Key Laboratory of Crop Biology / Shandong Key Laboratory of Crop Biology / College of Agriculture, Shandong Agricultural University, Tai’an 271018, China; 2 College of Life Sciences, Shandong Agricultural University, Tai’an 271018, China
  • Received:2012-07-06 Revised:2013-01-15 Published:2013-06-12 Published online:2013-02-19
  • Contact: 万勇善, E-mail: yswan@sdau.edu.cn, Tel: +86 (0)538 8241540

摘要:

以抗旱性强的花生品种丰花5号为材料,利用Solexa高通量测序技术15% PEG处理后的花生叶片cDNA文库进行差异基因表达谱分析。结果表明,转录组基因表达表现出高度的不均一性和冗余性,低于10个拷贝的标签占总标签种类的73.1%,但其表达量只占总标签表达量的9.0%。根据已知序列信息鉴定出935个差异表达基因,其中64.5%下调表达。基因功能分析表明,差异表达基因广泛涉及糖、蛋白、核酸和脂类等生物大分子代谢、能量代谢以及次生代谢过程。在花生干旱响应基因表达谱分析中,发现9个类黄酮代谢相关基因在干旱胁迫下显著上调表达,其中4个编码类黄酮合成酶类,3个编码甲基转移酶,2个编码MYB转录因子。通过半定量RT-PCR对花生苯丙氨酸解氨酶基因(AhPAL)表达分析表明,15%PEG干旱胁迫6 h诱导该基因显著表达。推测类黄酮代谢在花生干旱胁迫响应中起重要作用。

关键词: 花生, 干旱, 高通量测序, 基因表达谱

Abstract:

Drought, one of the most important abiotic stresses, usually causes adverse effects on the productivity and quality of crops. In this study, a drought-resistant variety Fenghua 5 was used to analyse leaf cDNA library of peanut treated with 15% PEG by Solexa high-throughput technology, and detect the differentially expressed genes under drought stress. The results of Solexa sequencing indicated the gene expression in peanut transcriptome presented strong nonhomogeneity and redundancy. The sequenced tags less than 10 copies accounted for 73.1% of the total tag types, however its expression level only accounted for 9.0% of the total. A total of 935 differentially expressed genes were screened out based on the reference tags, of which 64.5% were down-regulated. These differentially expressed genes were involved in metabolisms of carbohydrate, protein, nucleic acid, lipid and energy, and secondary metabolism. Gene expression analysis of peanut also showed that nine transcripts related to flavonoid metabolism significantly up-regulated under drought stress, including four encoding flavonoid biosynthesis enzymes, three encoding methyltransferase and two encoding MYB transcription factor. The gene expression analysisusing semi-quantitative RT-PCR assays indicated that AhPAL was induced significantly by 15% PEG treatment for 6 h. The result showed that flavonoids metabolism might play an important role in peanut responding to drought stress.

Key words: Peanut, Drought, High-throughput sequencing, Gene expression profile

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