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Selection of Reference Genes for Real-time Quantitative PCR Normalization in the Process of Gaeumannomyces graminis var. tritici Infecting Wheat.


ABSTRACT: Gaeumannomyces graminis var. tritici is a soil borne pathogenic fungus associated with wheat roots. The accurate quantification of gene expression during the process of infection might be helpful to understand the pathogenic molecular mechanism. However, this method requires suitable reference genes for transcript normalization. In this study, nine candidate reference genes were chosen, and the specificity of the primers were investigated by melting curves of PCR products. The expression stability of these nine candidates was determined with three programs-geNorm, Norm Finder, and Best Keeper. TUB? was identified as the most stable reference gene. Furthermore, the exopolygalacturonase gene (ExoPG) was selected to verify the reliability of TUB? expression. The expression profile of ExoPG assessed using TUB? agreed with the results of digital gene expression analysis by RNA-Seq. This study is the first systematic exploration of the optimal reference genes in the infection process of Gaeumannomyces graminis var. tritici.

SUBMITTER: Xie LH 

PROVIDER: S-EPMC6385657 | biostudies-literature | 2019 Feb

REPOSITORIES: biostudies-literature

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Selection of Reference Genes for Real-time Quantitative PCR Normalization in the Process of <i>Gaeumannomyces graminis</i> var. <i>tritici</i> Infecting Wheat.

Xie Li-Hua LH   Quan Xin X   Zhang Jie J   Yang Yan-Yan YY   Sun Run-Hong RH   Xia Ming-Cong MC   Xue Bao-Guo BG   Wu Chao C   Han Xiao-Yun XY   Xue Ya-Nan YN   Yang Li-Rong LR  

The plant pathology journal 20190201 1


<i>Gaeumannomyces graminis</i> var. <i>tritici</i> is a soil borne pathogenic fungus associated with wheat roots. The accurate quantification of gene expression during the process of infection might be helpful to understand the pathogenic molecular mechanism. However, this method requires suitable reference genes for transcript normalization. In this study, nine candidate reference genes were chosen, and the specificity of the primers were investigated by melting curves of PCR products. The expr  ...[more]

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