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Acta Horticulturae Sinica ›› 2026, Vol. 53 ›› Issue (2): 598-612.doi: 10.16420/j.issn.0513-353x.2025-0772

• Research Papers • Previous Articles     Next Articles

Screening and Validation of Reference Genes for qRT-PCR Analysis of Genes Related to Floral Scent Biosynthesis in Camellia japonica

CHEN Yiquan, FAN Ronghui, LIN Bing, CHEN Yan, WU Jianshe(), ZHONG Huaiqin()   

  1. Fujian Engineering Research Center for Characteristic Floriculture,Institute of Crop Sciences(Fujian Germplasm Resources Center),Fujian Academy of Agricultural Sciences,Fuzhou 350013,China
  • Received:2025-08-08 Revised:2026-01-06 Online:2026-02-25 Published:2026-02-12

Abstract:

To study the expression patterns of genes related to floral scent biosynthesis in Camellia japonica and screen for stably expressed reference genes. Quantitative real-time PCR(qRT-PCR)technology was used to detect the expression levels of 10 candidate reference genes(α-TUBCYPPP2AACTIN1ACTIN2GAPDHUBQAQPUBC,and HIS)in different tissues,flowering stages,cultivars and mixed samples. The stability of internal reference genes was comprehensively evaluated and identified using four algorithms:geNorm,NormFinder,BestKeeper,and RefFinder. The results showed that the primer specificity of the 10 candidate reference genes was good,and all of them had the performance as reference genes. PP2A and UBC can be used for analyzing gene expression at different flowering stages. The most ideal reference genes for analyzing gene expression in different tissues and fragrance cultivars were identified as PP2A and ACTIN1. PP2A can be stably expressed in different tissues,flowering stages,fragrance cultivars and mixed samples. Nine floral scent-related target genes were amplified by qRT-PCR,and PP2A is the optimal reference gene for studying the expression of floral scent-related genes in Camellia japonica. However,when the traditional housekeeping gene GAPDH was used as the reference gene,significant deviations were observed in the expression patterns of the linalool/nerolidol synthase gene(CaLIS/NES1)and the phenylacetaldehyde reductase gene(CaPAR).

Key words: Camellia japonica, floral scent, reference gene, quantitative real-time PCR, expression analysis, PP2A