首页> 外文期刊>Plant Growth Regulation: An International Journal on Natural and Synthetic Regulators >Transcription factor TERF1 regulates nuclear genes expression through miRNAs in tobacco under drought stress condition
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Transcription factor TERF1 regulates nuclear genes expression through miRNAs in tobacco under drought stress condition

机译:转录因子Terf1通过在干旱胁迫条件下通过MiRNA调节核基因表达

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摘要

Ethylene is an important phytohormone that regulates plant response to drought stress. ETHYLENE RESPONSE FACTOR 1 (ERF1), a transcription factor of ERF/AP2 family, plays an important role in activating ethylene signaling pathway through binding the GCC box in the promoters of ethylene responsive genes. Although we know some protein-coding genes regulated by ERF1, we know nothing about how ERF1 regulates the expression of miRNAs. We utilized the tobacco overexpressing TOMATO ETHYLENE RESPONSE FACTOR1 (TERF1), an ERF1 transcription factor isolated from tomato, to investigate the miRNAs expression profile under natural dehydration condition by method of qRT-PCR. Results show that 25 miRNAs are significantly induced and only 10 miRNAs are significantly repressed by TERF1. Binding sites for ERF transcription factors are observed in six upregulated miRNAs and the core genes involved in the processing of pre-miRNA are also significantly induced by TERF1. We predicted the target genes regulated by the differentially expressed miRNAs by the on-line programme of psRNATarget. Gene ontology (GO) analysis shows that the significantly enriched biological processes for the target genes regulated by the downregulated miRNAs are located in chloroplast. We also predicted the important regulatory genes regulated by the differentially expressed miRNAs, including transcription factors, kinases and phosphatases. Our research provides novel mechanism for regulation of nuclear genes expression by TERF1 at posttranscriptional level under drought stress condition.
机译:乙烯是调节对干旱胁迫的植物反应的重要植物激素。乙烯响应因子1(ERF1),ERF / AP2家族的转录因子,在激活乙烯信号通路中发挥着重要作用,通过结合乙烯响应基因的启动子中的GCC盒。虽然我们了解由ERF1调节的一些蛋白质编码基因,但我们对ERF1如何调节MIRNA的表达,但我们都不了解。我们利用烟草过表达番茄乙烯响应因子1(TERF1),一种从番茄中分离的ERF1转录因子,通过QRT-PCR的方法研究天然脱水条件下的miRNA表达谱。结果表明,25 miRNA被显着诱​​导,只有10 miRNA被TERF1大大压制。在六个上调的miRNA中观察到ERF转录因子的结合位点,并且TERF1也显着地诱导了六个上调的miRNA和参与的核心基因的核心基因。我们预测了由PSRNATarget的在线程序由差异表达的miRNA调节的目标基因。基因本体论(GO)分析表明,下调MiRNA调节的靶基因的显着富集的生物方法位于叶绿体中。我们还预测了由差异表达的miRNA调节的重要调节基因,包括转录因子,激酶和磷酸酶。我们的研究提供了在干旱胁迫条件下在术后术语术后核基因调节核基因表达的新机制。

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