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Background <p>Real-time quantitative reverse transcription PCR (qRT-PCR) is a widely used technique for gene expression analysis, and its accuracy depends critically on stable reference genes for normalization. Bitter gourd (<i>Momordica charantia</i> L.), an annual cucurbit valued for both nutritional and medicinal properties, has recently attracted increasing attention in molecular research. However, systematic evaluation of suitable reference genes in this species remains lacking.</p> Results <p>In this study, eight candidate reference transcripts—<i>McFBX</i>, <i>McARMT</i>, <i>McEXO70</i>, <i>McALDH12A1</i>, <i>McCPR5</i>, <i>McDRB2</i>, <i>McBLOC1S1</i>, and <i>McNPF4.6</i>—were identified through integrated analysis of three public bitter gourd transcriptome datasets, based on high expression abundance and low variability. Their expression stability was evaluated across tissues, genotypes, and treatment conditions of bitter gourd using three commonly applied algorithms: geNorm, NormFinder, and BestKeeper, and RefFinder was subsequently used to perform a comprehensive stability ranking of these reference transcripts. For tissue-specific qRT-PCR, all eight genes showed acceptable stability, with <i>McFBX</i> being the most stable, followed by <i>McNPF4.6</i>. Under stress and hormone treatments, <i>McARMT</i> and <i>McNPF4.6</i> were identified as the most appropriate controls, while <i>McEXO70</i> was best suited for complex experimental designs involving multiple tissues, genotypes, and treatments.</p> Conclusion <p>By broadening the evaluation framework, this study systematically validated the universality and reliability of reference genes under diverse scenarios. These findings provide a robust set of internal controls for accurate qRT-PCR analyses in bitter gourd and will improve the reproducibility of future molecular studies in this species.</p>

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Evaluation of reference genes for accurate qRT-PCR normalization in bitter gourd across different tissues and stress conditions

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年12月12日

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  • Shihan Zeng,
  • Tian Xie,
  • Xiaoqi Shu,
  • Zhuning Zhou,
  • Daiyue Yang,
  • Hongrui Ma,
  • Xuzhen Li,
  • Feifan Chen,
  • Libo Tian,
  • Sang Shang

摘要

Background

Real-time quantitative reverse transcription PCR (qRT-PCR) is a widely used technique for gene expression analysis, and its accuracy depends critically on stable reference genes for normalization. Bitter gourd (Momordica charantia L.), an annual cucurbit valued for both nutritional and medicinal properties, has recently attracted increasing attention in molecular research. However, systematic evaluation of suitable reference genes in this species remains lacking.

Results

In this study, eight candidate reference transcripts—McFBX, McARMT, McEXO70, McALDH12A1, McCPR5, McDRB2, McBLOC1S1, and McNPF4.6—were identified through integrated analysis of three public bitter gourd transcriptome datasets, based on high expression abundance and low variability. Their expression stability was evaluated across tissues, genotypes, and treatment conditions of bitter gourd using three commonly applied algorithms: geNorm, NormFinder, and BestKeeper, and RefFinder was subsequently used to perform a comprehensive stability ranking of these reference transcripts. For tissue-specific qRT-PCR, all eight genes showed acceptable stability, with McFBX being the most stable, followed by McNPF4.6. Under stress and hormone treatments, McARMT and McNPF4.6 were identified as the most appropriate controls, while McEXO70 was best suited for complex experimental designs involving multiple tissues, genotypes, and treatments.

Conclusion

By broadening the evaluation framework, this study systematically validated the universality and reliability of reference genes under diverse scenarios. These findings provide a robust set of internal controls for accurate qRT-PCR analyses in bitter gourd and will improve the reproducibility of future molecular studies in this species.