The Identification of the Banana Endogenous Reference Gene and the Construction of Qualitative and Quantitative PCR Detection Methods.

Lili Zhu, Ying Lin, Wenli Yang, Zhiwen Pan, Weiting Chen, Juan Yao, Ou Sheng, Lingyan Zhou, Dagang Jiang
Author Information
  1. Lili Zhu: College of Life Sciences, South China Agricultural University, Guangzhou 510642, China.
  2. Ying Lin: College of Life Sciences, South China Agricultural University, Guangzhou 510642, China.
  3. Wenli Yang: College of Life Sciences, South China Agricultural University, Guangzhou 510642, China.
  4. Zhiwen Pan: College of Life Sciences, South China Agricultural University, Guangzhou 510642, China. ORCID
  5. Weiting Chen: College of Life Sciences, South China Agricultural University, Guangzhou 510642, China.
  6. Juan Yao: College of Life Sciences, South China Agricultural University, Guangzhou 510642, China.
  7. Ou Sheng: Institute of Fruit Tree Research, Guangdong Academy of Agricultural Sciences, Guangzhou 510640, China. ORCID
  8. Lingyan Zhou: College of Agriculture & Biology, Zhongkai University of Agriculture and Engineering, Guangzhou 510225, China.
  9. Dagang Jiang: College of Life Sciences, South China Agricultural University, Guangzhou 510642, China.

Abstract

Endogenous reference genes play a crucial role in the qualitative and quantitative PCR detection of genetically modified crops. Currently, there are no systematic studies on the banana endogenous reference gene. In this study, the gene was identified as a candidate gene through bioinformatics analysis. The conservation of this gene in different genotypes of banana was tested using PCR, and its specificity in various crops and fruits was also examined. Southern blot analysis showed that there is only one copy of in banana. The limit of detection (LOD) test showed that the LOD of the conventional PCR method is approximately 20 copies. The real-time fluorescence quantitative PCR (qPCR) method also exhibited high specificity, with a LOD of approximately 10 copies. The standard curve of the qPCR method met the quantitative requirements, with a limit of quantification (LOQ) of 1.14 × 10 ng-about 20 copies. Also, the qPCR method demonstrated good repeatability and stability. Hence, the above results indicate that the detection method established in this study has strong specificity, a low detection limit, and good stability. It provides a reliable qualitative and quantitative detection system for banana.

Keywords

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Grants

  1. 2023ZD04062/the Science and Technology Innovation 2030

MeSH Term

Musa
Plants, Genetically Modified
Crops, Agricultural
Real-Time Polymerase Chain Reaction

Word Cloud

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