4.7 Article

Reference Genes for Expression Analysis Using RT-qPCR in Cnaphalocrocis medinalis (Lepidoptera: Pyralidae)

Journal

INSECTS
Volume 13, Issue 11, Pages -

Publisher

MDPI
DOI: 10.3390/insects13111046

Keywords

reference genes; migratory insect; Cnaphalocrocis medinalis; RT-qPCR; expression stability

Categories

Funding

  1. National Natural Science Foundation of China
  2. Zhejiang Provincial Natural Science Foundation of China
  3. earmarked fund for China Agriculture Research System
  4. [32202280]
  5. [LQ22C140006]
  6. [CARS-01]

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This study identified stable reference genes for the rice pest Cnaphalocrocis medinalis under different experimental conditions. The results showed that EF1 beta, PGK, and RPL18 were the most stable reference genes. These findings provide a reliable RT-qPCR analysis method for future gene function studies in this pest.
Simple Summary The reference gene is the key to verifying the relative expression of target genes. However, the expression of common housekeeping genes is not stable under different experimental conditions, which may lead to misleading gene expression results. In this study, the stability of thirteen housekeeping genes of the rice pest Cnaphalocrocis medinalis at different developmental stages, larvae tissues, rice feedings, temperature treatments, and adult ages, nutritional conditions, mating statuses and different take-off characteristics was identified. Finally, the relative expression of Trypsin-3 in different rice varieties was evaluated to verify the reliability of the results. Our results will help to improve the accuracy of RT-qPCR analysis and lay a foundation for the analysis of target gene expression for C. medinalis in the future. Cnaphalocrocis medinalis is a destructive migratory rice pest. Although many studies have investigated its behavioral and physiological responses to environmental changes and migration-inducing factors, little is known about its molecular mechanisms. This study was conducted to select suitable RT-qPCR reference genes to facilitate future gene expression studies. Here, thirteen candidate housekeeping genes (EF1 alpha, AK, EF1 beta, GAPDH, PGK, RPL13, RPL18, RPS3, 18S rRNA, TBP1, TBP2, ACT, and UCCR) were selected to evaluate their stabilities under different conditions using the increment CT method; the geNorm, NormFinder, BestKeeper algorithms; and the online tool RefFinder. The results showed that the most stable reference genes were EF1 beta, PGK, and RPL18, related to developmental stages; RPS3 and RPL18 in larval tissues; EF1 beta and PGK in larvae feeding on different rice varieties; EF1 alpha, EF1 beta, and PGK in larvae temperature treatments; PGK and RPL13, related to different adult ages; PGK, EF1 alpha, and ACT, related to adult nutritional conditions; RPL18 and PGK, related to adult mating status; and, RPS3 and PGK, related to different adult take-off characteristics. Our results reveal reference genes that apply to various experimental conditions and will greatly improve the reliability of RT-qPCR analysis for the further study of gene function in this pest.

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