論文

2018年

Evaluation of internal control genes for quantitative realtime PCR analyses for studying fruit development of dwarf tomato cultivar ‘Micro-Tom’

Plant Biotechnology
  • Choi, Seung-won
  • ,
  • Hoshikawa, Ken
  • ,
  • Fujita, Satoshi
  • ,
  • Thi, Dung Pham
  • ,
  • Mizoguchi, Tsuyoshi
  • ,
  • Ezura, Hiroshi
  • ,
  • Ito, Emi

35
3
開始ページ
225
終了ページ
235
記述言語
日本語
掲載種別
研究論文(学術雑誌)
DOI
10.5511/plantbiotechnology.18.0525a
出版者・発行元
日本植物細胞分子生物学会

Quantitative real-time PCR (qRT-PCR) is widely used to analyze the expression profiles of the genes of interest. In order to obtain accurate quantification data, normalization by using reliable internal control genes is essential. In this study, we evaluated the stability and applicability of eight internal control gene candidates for analyzing gene expression during fruit development in dwarf tomato cultivar Micro-Tom. We collected seventeen different samples from flowers and fruits at different developmental stages, and estimated the expression stability of the candidate genes by two statistical algorithms, geNorm and NormFinder. The combined ranking order and qRT-PCR analyses for expression profiles of SlYABBY2a, SlYABBY1a, FRUITFULL1 and APETALA2c suggested that EXPRESSED was the most stable and reliable internal control gene among the candidates. Our analysis also suggested that RPL8 was also suitable if the sample group is limited to fruits at different maturation stages. In addition to EXPRESSED, GAPDH was also applicable for relative quantitation to monitor gene expression profiles through fruit development from pistil

リンク情報
DOI
https://doi.org/10.5511/plantbiotechnology.18.0525a

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