文章摘要
Reference gene selection for real-time quantitativePCR normalization under fusaric acid stress inBenincasa hispida Cogn. var. chieh-qua How
  
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Author NameAffiliation
张金平1,2,3、何晓明2,3、江彪2,3、谢大森2,3、彭庆务2、王永飞1、马三梅1 1. 暨南大学生命科学技术学院、广东广州5106322.广东省农科院蔬菜研究所、广东广州510640 3.广东蔬菜新技术研究重点试验室、广东广州510640 
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Abstract:
      Appropriate reference genes for specific experimental materials and conditions are critical for analyzing the expression of target gene by real-time quantitative PCR. In this study, four common housekeeping genes GAPDH, Actin, UBQ, CYP and two novel reference genes CACS, F-box were chosen for identifying the expression stability in Benincasa hispida Cogn. var. chieh-qua How samples from various plant tissues (roots, stems and leaves) or under fusaric acid (FA) stress. The expression stability of candidate genes was determined and ranked using RefFinder software. The results revealed a remarkably stable expression pattern of Actin and F-box when samples were stressed by fusaric acid. F-box gene showed the most stable expression level in different tissues. Additionally, expression of traditional housekeeping genes GAPDH and CYP showed great variations and therefore they were considered unsuitable as reference genes. This study has laid the foundation for the study of resistance-related genes expression for fusarium wilt in B. hispida Cogn. var. chieh-qua How
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