Biotechnology Bulletin ›› 2026, Vol. 42 ›› Issue (2): 158-168.doi: 10.13560/j.cnki.biotech.bull.1985.2025-0378

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Screening of Internal Reference Gene for Pholidota chinensis and Their Applications

LIU Bao-cai1,2,3(), HU Xue-bo2, ZHANG Wu-jun1,3, ZHAO Yun-qing1,3, HUANG Ying-zhen1,3, CHEN Jing-ying1,3()   

  1. 1.Institute of Crop Sciences, Fujian Academy of Agricultural Sciences, Fuzhou 350003
    2.College of Plant Science and Technology, Huazhong Agricultural University, Wuhan 430070
    3.Research Center for Medicinal Plant, Fujian Academy of Agricultural Sciences, Fuzhou 350003
  • Received:2025-04-11 Online:2026-02-26 Published:2026-03-17
  • Contact: CHEN Jing-ying E-mail:626813844@qq.com;cjy6601@163.com

Abstract:

Objective Pholidota chinensis is a rare and endangered perennial epiphytic medicinal plant of the Orchidaceae family. To study the expressions of functional genes in this species and its closely related species, it is timely to screen for stable housekeeping genes in real-time fluorescent quantitative PCR (RT-qPCR) analysis. Method The RT-qPCR was used to detect the expression of 11 housekeeping genes in different tissues (roots, rhizomes, pseudobulbs, leaves, buds, and flowers) and abiotic stresses (20 mmol/L MeJA sprayed leaves for 24 h and 48 h, 50 mmol/L NaCl sprayed leaves for 24 h and 48 h, and different light intensities) in P. chinensis. The expression stability of 11 candidate internal reference genes was analyzed by geNorm, NormFinder, BestKeeper, ΔCt, and geometric mean values from RefFinder. Result The results revealed single extended bands and peak maps for eleven genes. Although the amplification efficiency and expression abundance of eleven genes met the requirements expected of internal reference genes, the expression stability analysis indicated that Actin/f58p0 was the best internal reference gene for gene expression analysis in different tissues. Conversely, TUA3/f11p0 was favored as the internal reference gene for abiotic stress analysis. The expression trends of key genes involved in gastrodin biosynthesis, namely GT1, GT2, GT3-01, GT3-02, GT4, ADH-01, ADH-02, and ADH-03, were generally consistent across different tissues by using Actin/f58p0 and TUA3/f11p0 as internal reference genes. However, the Actin/f58p0 was more suitable as an internal reference gene for the shikimate O-hydroxycinnamoyltransferase gene (HCT). Under abiotic stress conditions, the TUA3/f11p0 was a better internal reference gene, especially under NaCl and MeJA treatments. However, under light stress, the Actin/f58p0 and TUA3/f11p0 were both as internal references. MeJA had a longer-lasting effect on gene expressions than NaCl. Conclusion This study identifies Actin/f58p0 and TUA3/f11p0 as reliable internal reference genes for analyzing gene expression in different tissues and under abiotic stresses in P. chinensis. These findings lay a foundation for research on functional gene discovery and expression analysis in P. chinensis and related species.

Key words: Pholidota chinensis, internal reference genes, tissue, light, NaCl, MeJA, RT-qPCR, gene expression