中国水稻科学 ›› 2019, Vol. 33 ›› Issue (1): 75-84.DOI: 10.16819/j.1001-7216.2019.8035

• 实验技术 • 上一篇    下一篇

二化螟实时荧光定量PCR内参基因筛选和表达稳定性评价

徐红星1, 王国荣2, 鲁艳辉1,*(), 杨亚军1, 郑许松1, 田俊策1, 吕仲贤1,*()   

  1. 1浙江省农业科学院 农业部农产品信息溯源重点实验室/省部共建国家重点实验室培育基地, 杭州 310021
    2杭州市萧山区农业技术推广中心, 杭州 311202
  • 收稿日期:2018-03-27 修回日期:2018-05-15 出版日期:2019-01-10 发布日期:2019-01-10
  • 通讯作者: 鲁艳辉,吕仲贤
  • 基金资助:
    国家自然科学基金资助项目(31672050);浙江省植物有害生物防控省部共建国家重点实验室培育基地自主设计项目(2010DS700124- ZZ1601)

Screening Reference Genes and Evaluating of Their Expression Stability for qRT-PCR Normalization in Chilo suppressalis (Lepidoptera: Pyralididae)

Hongxing XU1, Guorong WANG2, Yanhui LU1,*(), Yajun YANG1, Xusong ZHENG1, Junce TIAN1, Zhongxian LÜ1,*()   

  1. 1Key Laboratory of Information Traceability for Agricultural Products, Ministry of Agriculture, P. R. of China/Key Laboratory Breeding Base for Zhejiang Sustainable Pest and Disease Control, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, China
    2Xiaoshan Agricultural Technology Extension Center, Hangzhou 311202, China
  • Received:2018-03-27 Revised:2018-05-15 Online:2019-01-10 Published:2019-01-10
  • Contact: Yanhui LU, Zhongxian LÜ

摘要:

【目的】筛选特定试验条件下二化螟(Chilo suppressalis)稳定表达的内参基因,为二化螟基因表达研究奠定基础。【方法】根据二化螟转录组测序结果挑选出11个候选基因,利用实时荧光定量PCR测定其在二化螟不同发育历期、不同组织、温度处理、杀虫剂处理、取食不同饲料、取食不同水稻、dsRNA处理和混合样品的表达量,利用RefFinder、BestKeeper、GeNorm和NormFinder等软件和ΔCt值对11个候选基因的稳定性进行评估。【结果】5种分析方法表明,在二化螟不同发育历期稳定性较高的内参基因是AKRPL10EF1,不同组织中稳定性较高的内参基因是EF1TUBACTB,不同温度下较稳定的内参基因为TUBRPL10EF1,杀虫剂处理样品中较稳定的是TF4ACTA,取食不同饲料较稳定的是TUBTF4EF1RPL10,取食不同品种水稻较稳定的是TUBEF1,dsRNA处理样品中较稳定的是TUBAKACTBEF1,混合样品中较稳定的是EF1、TUBACTB。【结论】为不同试验条件下选择合适的内参基因提供了参考,也有利于在二化螟基因表达研究中获得更加可靠准确的数据。

关键词: 二化螟, 内参基因, 荧光定量PCR, 基因表达

Abstract:

【Objective】We aim to screen reference genes stably expressed in striped stem borers (SSB), Chilo suppressalis, under certain conditions, to lay a foundation for the study on the gene expression in SSB. 【Method】According to the results of SSB transcriptome data, 11 candidate genes from SSB were selected and their expression stability was detected under different treatment conditions (including development duration, tissues, feeding on different diets and rice varieties, dsRNA and mixed samples under temperature stress, insecticide treatment), by using real-time fluorescence quantitative PCR. The stability of the 11 candidate genes was evaluated by RefFinder, BestKeeper, GeNorm, NormFinder and ΔCt. 【Result】AK, RPL10 and EF1 were highly stable in different development durations; EF1, TUB and ACTB were highly stable in different tissues. TUB, RPL10 and EF1 were relatively stable under temperature stress. TF4 and ACTA were stable in insecticide treated samples. TUB, TF4, EF1 and RPL10 were stable in samples fed on different diets. TUB and EF1 were stable reference genes in samples fed on different rice varieties. TUB, AK, ACTB and EF1 were stable in the sample treated with dsRNA. EF1, TUB and ACTB were stable in mixed samples. 【Conclusion】 It provide a reference for selection of suitable reference gene under different test conditions, and also provide more reliable and accurate data for research in gene expression in rice SSB.

Key words: Chilo suppressalis, reference gene, qRT-PCR, gene expression

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