大豆ERF转录因子基因GmERF8的克隆与表达分析
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国家自然科学基金项目(面上项目,重点项目,重大项目)


Cloning and Expression Analysis of ERF Transcription Factor GmERF8 in Soybean
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The National Natural Science Foundation of China (General Program, Key Program, Major Research Plan)

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    摘要:

    ERF转录因子广泛存在于植物中并且参与植物对生物及非生物胁迫的响应。利用RT-PCR技术从大豆中克隆了1个新的ERF转录因子基因GmERF8。此基因开放阅读框全长627 bp,编码1个由208个氨基酸残基组成,分子量为23.43 kD的蛋白。蛋白结构预测发现,该蛋白含有1个典型AP2/ERF结合域,两个预测的核定位信号和1个保守的EAR抑制元件。进化分析表明GmERF8蛋白与烟草NtERF3蛋白的同源性最高。实时荧光定量PCR表明,GmERF8在大豆的根和叶中表达量较高。ABA、高盐和低温处理均使GmERF8表达量下降;乙烯(ET)和干旱处理则使GmERF8的表达量先下降后升高。转录调节能力分析结果显示, GmERF8可以抑制报告基因的表达。上述实验结果表明,GmERF8可能作为转录抑制子参与大豆对环境胁迫的应答。

    Abstract:

    ERF transcription factors are widespread in plants, which are widely involved in plant response to biotic and abiotic stress. In this research, a gene GmERF8 encoding a new ERF protein was isolated using RT-PCR from soybean. GmERF8 consisted of an ORF (open reading frame) with a length of 627 bp , and encoded a 23.43 kDa protein with 208 amino acids. Bioinformatics analysis indicated that GmERF8 contained a typical AP2/ERF binding domain, two putative nuclear localization signal sequences and a conserved repression-associated EAR motif. The amino acid sequences of GmERF8 and NtERF3 shared high homology through phylogenetic analysis. Real-time fluorescence quantitative PCR results revealed that GmERF8 expressed highly in roots and leaves. The expression of GmERF8 decreased under ABA, salt and cold treatments. Whereas it decreased firstly and thereafter increased under ethylene and drought treatments. Transcription regulation experiments demonstrated that GmERF8 downregulated the transcriptional level of the reporter gene. As the result, GmERF8 may founctions as a transcriptional repressor in soybean to response to environmental stress.

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翟莹,张军,赵艳,等.大豆ERF转录因子基因GmERF8的克隆与表达分析[J].植物遗传资源学报,2016,17(6):1036-1040.

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  • 收稿日期:2016-01-18
  • 最后修改日期:2016-03-26
  • 录用日期:2016-04-21
  • 在线发布日期: 2016-11-08
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