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铁皮石斛DcNAC48基因的克隆及表达分析

Cloning and Expression Analysis of DcNAC48 Gene of Dendrobium catenatum Lindl.

  • 摘要: 以铁皮石斛(Dendrobium catenatum Lindl.)为试材,采用PCR技术从中克隆一个NAC(NAM,ATAF1/2,CUC2)转录因子基因DcNAC48,利用生物信息学技术分析该基因的特征结构,采用荧光定量PCR方法研究了该基因在不同组织部位和不同胁迫下的表达模式,以期为进一步研究该基因功能奠定基础,为提高铁皮石斛抗逆性提供基因资源。结果表明:DcNAC48基因全长909 bp,编码302个氨基酸,具有NAC保守结构域,在其基因启动子区存在多种激素响应元件、逆境响应元件、生长发育响应元件以及光响应元件。不同组织部位表达分析表明DcNAC48具有组织表达特异性,在合蕊柱中表达量最高。不同胁迫处理下的基因表达模式表明DcNAC48受低温胁迫、盐胁迫、干旱胁迫和高温胁迫的诱导而上调表达,推测该基因可能参与铁皮石斛对非生物胁迫的响应。

     

    Abstract: A NAC(NAM,ATAF1/2,CUC2) transcription factor gene DcNAC48 was cloned by PCR from Dendrobium catenatum Lindl..The characteristic structures of the gene were analyzed by bioinformatics and the expression patterns in different tissues and under different stresses were studied by quantitative real-time PCR(qRT-PCR),in order to lay a foundation for further study of the function of DcNAC48 and provide gene resources for improving the stress resistance of D.catenatum.The results showed that the total length of DcNAC48 gene was 909 bp, encoding 302 amino acids, and had a conserved NAC domain.There were various hormone responsive elements, stress responsive elements, growth and development responsive elements and light responsive elements in the gene promoter region.The expression patterns analysis showed that DcNAC48 had tissue specificity, and its expression level was the highest in the gynostemium.The gene expression patterns under different stress treatments indicated that DcNAC48 was upregulated by low temperature, salt stress, drought stress and high temperature stress, suggesting that DcNAC48 might be involved in the response of D.catenatum Lindl.to abiotic stress.

     

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