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Selection and verification of candidate reference genes for gene expression by quantitative RT-PCR in Hibiscus hamabo Sieb.et Zucc.

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Ten candidate reference genes were examined in Hibiscus hamabo Sieb. et Zucc. ACT and SKIP are proposed as good reference genes for gene studies in Hibiscus hamabo Sieb. et Zucc.

Abstract

Because of its sensitivity and rapidness, quantitative real-time PCR (qRT-PCR) is currently extensively used to analyze gene-expression patterns. Selecting suitable reference genes to normalize qRT-PCR results is essential. Hibiscus hamabo Sieb. et Zucc. (H. hamabo) is a semi-mangrove plant that is widely used for the ecological restoration of saline-alkali land and coastal afforestation owing to its excellent salt tolerance. However, suitable reference genes used for the normalization of H. hamabo qRT-PCR data have not been selected or verified. Here, we tested the expression stabilities of ten candidate reference genes in different H. hamabo tissues under a set of abiotic stresses (salt, drought, high temperature, and low temperature) and hormonal treatments (methyl jasmonate, abscisic acid, and salicylic acid) using three statistical algorithms, i.e., NormFinder, geNorm, and BestKeeper. Actin (ACT) and ski-interacting protein (SKIP) can be regarded as good choices as reference genes in studying gene expression of H. hamabo. In addition, the qRT-PCR analysis of the NAC (NAM/ATAF1/2/CUC2) target gene’s expression pattern under NaCl-treated conditions confirmed the suitability of selected reference genes. Here, we used qRT-PCR technology to provide a stable reference gene list for H. hamabo gene-expression studies.

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References

  • Borowski JM, Galli V, da Silva Messias R, Perin EC, Buss JH, Silva SDA, Rombaldi CV (2014) Selection of candidate reference genes for real-time PCR studies in lettuce under abiotic stresses. Planta 239:1187–1200

    CAS  PubMed  Google Scholar 

  • Campos MD, Frederico AM, Nothnagel T, Arnholdt-Schmitt B, Cardoso H (2015) Selection of suitable reference genes for reverse transcription quantitative real-time PCR studies on different experimental systems from carrot (Daucus carota L.). Sci Hortic 186:115–123

    Article  CAS  Google Scholar 

  • Deinlein U, Stephan AB, Horie T, Luo W, Xu G, Schroeder JI (2014) Plant salt-tolerance mechanisms. Trends Plant Sci 19:371–379

    Article  CAS  Google Scholar 

  • Fernandez P, Rienzo JAD, Moschen S, Dosio GAA, Aguirrezábal LAN, Hopp HE, Paniego N, Heinz RA (2011) Comparison of predictive methods and biological validation for qPCR reference genes in sunflower leaf senescence transcript analysis. Plant Cell Rep 30:63–74

    Article  CAS  Google Scholar 

  • Golldack D, Lüking I, Yang O (2011) Plant tolerance to drought and salinity: stress regulating transcription factors and their functional significance in the cellular transcriptional network. Plant Cell Rep 30:1383–1391

    Article  CAS  Google Scholar 

  • Gu C, Chen S, Liu Z, Shan H, Luo H, Guan Z, Chen F (2011) Reference gene selection for quantitative real-time PCR in Chrysanthemum subjected to biotic and abiotic stress. Mol Biotechnol 49:192–197

    Article  CAS  Google Scholar 

  • Gu C, Liu L, Xu C, Zhao Y, Zhu X, Huang S (2014) Reference gene selection for quantitative real-time RT-PCR normalization in Iris lactea var. chinensis roots under cadmium, lead, and salt stress conditions. Sci World J 2014:532713

    Google Scholar 

  • Gu C, Liu L, Song A, Liu Z, Zhang Y, Huang S (2018a) Iris lactea var. chinensis (Fisch.) cysteine-rich gene llCDT1 enhances cadmium tolerance in yeast cells and Arabidopsis thaliana. Ecotoxicol Environ Saf 157:67–72

    Article  CAS  Google Scholar 

  • Gu C, Xu S, Wang Z, Liu L, Zhang Y, Deng Y, Huang S (2018b) De novo sequencing, assembly, and analysis of Iris lactea var. chinensis roots’ transcriptome in response to salt stress. Plant Physiol Biochem 125:1–12

    Article  CAS  Google Scholar 

  • Kanakachari M, Solanke AU, Prabhakaran N, Ahmad I, Dhandapani G, Jayabalan N, Kumar PA (2015) Evaluation of suitable reference genes for normalization of qPCR gene expression studies in Brinjal (Solanum melongena L.) during fruit developmental stages. Appl Biochem Biotechnol 178:433–450

    Article  Google Scholar 

  • Kim BR, Nam HY, Kim SU, Kim SI, Chang YJ (2003) Normalization of reverse transcription quantitative-PCR with housekeeping genes in rice. Biotech Lett 25:1869

    Article  CAS  Google Scholar 

  • Kundu Patel, Anju Amita (2013) Defining reference genes for qPCR normalization to study biotic and; abiotic stress responses in Vigna mungo. Plant Cell Rep 32:1647–1658

    Article  CAS  Google Scholar 

  • Lam-Son Phan T, Kazuo N, Yoh S, Simpson SD, Yasunari F, Kyonoshin M, Miki F, Motoaki S, Kazuo S, Kazuko YS (2004) Isolation and functional analysis of Arabidopsis stress-inducible NAC transcription factors that bind to a drought-responsive cis-element in the early responsive to dehydration stress 1 promoter. Plant Cell 16:2481–2498

    Article  Google Scholar 

  • Li J, Guan M, Wang E, Zhang J (2012) Salt tolerance of Hibiscus hamabo seedlings: a candidate halophyte for reclamation areas. Acta Physiol Plant 34:1747–1755

    Article  CAS  Google Scholar 

  • Li J, Han J, Hu Y, Yang J (2016a) Selection of reference genes for quantitative real-time PCR during flower development in tree peony (Paeonia suffruticosa Andr.). Front Plant Sci 7:516

    PubMed  PubMed Central  Google Scholar 

  • Li J, Jia H, Han X, Zhang J, Sun P, Lu M, Hu J (2016b) Selection of reliable reference genes for gene expression analysis under abiotic stresses in the desert biomass Willow, Salix psammophila. Front Plant Sci 7:1505

    PubMed  PubMed Central  Google Scholar 

  • Liu Q, Wei C, Zhang MF, Jia GX (2016) Evaluation of putative reference genes for quantitative real-time PCR normalization in Lilium regale during development and under stress. PeerJ 4:e1837

    Article  Google Scholar 

  • Lopez-Pardo R, de Galarreta JIR, Ritter E (2013) Selection of housekeeping genes for qRT-PCR analysis in potato tubers under cold stress. Mol Breed 31:39–45

    Article  CAS  Google Scholar 

  • Manjarin R, Trottier NL, Weber PS, Liesman JS, Taylor NP, Steibel JP (2011) A simple analytical and experimental procedure for selection of reference genes for reverse-transcription quantitative PCR normalization data. J Dairy Sci 94:4950–4961

    Article  CAS  Google Scholar 

  • Maroufi A, Bockstaele EV, Loose MD (2010) Validation of reference genes for gene expression analysis in chicory (Cichorium intybus) using quantitative real-time PCR. BMC Mol Biol 11:15

    Article  Google Scholar 

  • Nicot N, Hausman JL, Evers D (2005) Housekeeping gene selection for real-time RT-PCR normalization in potato during biotic and abiotic stress. J Exp Bot 56:2907–2914

    Article  CAS  Google Scholar 

  • Pfaffl MW, Tichopad A, Prgomet C, Neuvians TP (2004) Determination of stable housekeeping genes, differentially regulated target genes and sample integrity: BestKeeper—excel-based tool using pair-wise correlations. Biotechnol Lett 26:509–515

    Article  CAS  Google Scholar 

  • Ruijter JM, Ramakers C, Hoogaars WMH, Karlen Y, Bakker O, Hoff MJB, Den Van, Moorman AFM (2009) Amplification efficiency: linking baseline and bias in the analysis of quantitative PCR data. Nucleic Acids Res 37:e45

    Article  CAS  Google Scholar 

  • Sheshadri SA, Nishanth MJ, Yamine V, Simon B (2018) Effect of melatonin on the stability and expression of reference genes in Catharanthus roseus. Sci Rep 8:2222

    Article  CAS  Google Scholar 

  • Tang X, Zhang N, Si H, Calderón-Urrea A (2017) Selection and validation of reference genes for RT-qPCR analysis in potato under abiotic stress. Plant Methods 13:85

    Article  Google Scholar 

  • Vandesompele J, Preter KD, Pattyn F, Poppe B, Roy NV, Paepe AD, Speleman F (2002) Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome Biol 3(research0034):0031

    Google Scholar 

  • Wang Z, Gu C, Xuan L, Hua J, Shi Q, Fan W, Yin Y, Yu F (2017) Identification of suitable reference genes in Taxodium ‘Zhongshanshan’ under abiotic stresses. Trees 31:1–12

    Article  Google Scholar 

  • Wei L, Miao H, Zhao R, Han X, Zhang T, Zhang H (2013) Identification and testing of reference genes for Sesame gene expression analysis by quantitative real-time PCR. Planta 237:873–889

    Article  CAS  Google Scholar 

  • Wu ZJ, Tian C, Jiang Q, Li XH, Zhuang J (2016) Selection of suitable reference genes for qRT-PCR normalization during leaf development and hormonal stimuli in tea plant (Camellia sinensis). Sci Rep 6:19748

    Article  CAS  Google Scholar 

  • Yang H, Du G, Wang K (2008) Study on the physiological characteristics of Hibiscus hamabo under stress. J Zhejiang For Sci Tech 28:43–47

    Google Scholar 

  • Yuan F, Lyu MJA, Leng BY, Zhu XG, Wang BS (2016) The transcriptome of NaCl-treated Limonium bicolor leaves reveals the genes controlling salt secretion of salt gland. Plant Mol Biol 91:241–256

    Article  CAS  Google Scholar 

  • Zhong H, Simons JW (1999) Direct comparison of GAPDH, beta-actin, cyclophilin, and 28S rRNA as internal standards for quantifying RNA levels under hypoxia. Biochem Biophys Res Commun 259:523–526

    Article  CAS  Google Scholar 

Download references

Acknowledgements

The study was supported by Six Talent Peaks Project of Jiangsu Province (NY-042) and the 333 Talents Project of Jiangsu Province (BRA2017498).

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Correspondence to Huogen Li or Chunsun Gu.

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Communicated by D. Peterson.

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Ni, L., Wang, Z., Liu, L. et al. Selection and verification of candidate reference genes for gene expression by quantitative RT-PCR in Hibiscus hamabo Sieb.et Zucc.. Trees 33, 1591–1601 (2019). https://doi.org/10.1007/s00468-019-01882-x

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