Skip to main content
Log in

Identification of MV-generated ROS responsive EST clones in floral buds of Litchi chinensis Sonn.

  • Original Paper
  • Published:
Plant Cell Reports Aims and scope Submit manuscript

Abstract

Key message

A suppression subtractive hybridization library was constructed using inflorescence primordia of ‘Nuomici’ litchi to identify EST clones responsive to MV-generated ROS. 93 ESTs could be aligned as unique gene sequences in the inflorescence primordia of litchi.

Abstract

Litchi is an evergreen woody tree widely cultivated in subtropical and tropical regions. However, defective flowering is a pending problem of litchi production. Our previous study indicated that reactive oxygen species (ROS) induced by methyl viologen dichloride hydrate (MV) promotes flowering in litchi. In the present study, a suppression subtractive hybridization (SSH) library was constructed using inflorescence primordia of ‘Nuomici’ with the aim to find out ROS responsive clones during floral differentiation. 1856 Expressed sequence tag (EST) clones were randomly selected. Clones carrying single exogenous fragments were screened by reverse northern analysis to identify those responsive to MV-generated ROS. A total of 783 differentially expressed EST clones were identified as MV responsive cDNA and were subjected to sequencing. Among them, 26 clones were represented more than three times. 783 clones were aligned to 93 unique gene sequences. The unique genes were classified into 9 categories. 16 % of them were involved in transport facilitation, 11 % in transcription regulation, 4 % in stress response, 9 % in carbohydrate metabolism, 1 % in secondary metabolism, 14 % in intracellular signaling, and 25 % in other metabolism, while 9 % were genes with unknown functions and 11 % were genes with no match in the database.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  • Abel S, Nguyen MD, Theologis A (1995) The PS-IAA4/5-like family of early auxin-inducible mRNAs in Arabidopsis thaliana. J Mol Biol 251:533–549

    Article  PubMed  CAS  Google Scholar 

  • Agarwal PK, Jha B (2010) Transcription factors in plants and ABA dependent and independent abiotic stress signaling. Biol Plant 54:201–2010

    Article  CAS  Google Scholar 

  • Ali AG, Lovatt CJ (1995) Relationship of polyamines to low-temperature stress-induced flowering of the ‘Washington’ navel orange (Citrus sinensis L. Osbeck). J Hortic Sci Biotech 70:491–498

    CAS  Google Scholar 

  • An HL, Roussot C, Suárez-López P, Corbesler L, Vincent C, Pineiro M, Hepworth S, Mouradov A, Justin S, Turnbull C, Coupland G (2004) CONSTANS acts in the phloem to regulate a systemic signal that induces photoperiodic flowering of Arabidopsis thaliana. Development 131:3615–3626

    Article  PubMed  CAS  Google Scholar 

  • Bañuelos GR, Argumedo R, Patel K, Ng V, Zhou F, Vellanoweth RL (2008) The developmental transition to flowering in Arabidopsis is associated with an increase in leaf chloroplastic lipoxygenase activity. Plant Sci 174:366–373

    Article  PubMed  Google Scholar 

  • Bartosz G (1997) Oxidative stress in plants. Acta Physiol Plant 19:47–64

    Article  CAS  Google Scholar 

  • Blilou I, Xu J, Wildwater M, Willemsen V, Paponov I, Friml J, Heidstra R, Aida M, Palme K, Scheres B (2005) The PIN auxin efflux facilitator network controls growth and patterning in Arabidopsis roots. Nature 433:39–44

    Article  PubMed  CAS  Google Scholar 

  • Chauhan N, Khurana AK, Tyagi JP, Khurana P (2011) Identification and characterization of high temperature stress responsive genes in bread wheat (Triticum aestivum L.) and their regulation at various stages of development. Plant Mol Biol 75:35–51

    Article  PubMed  CAS  Google Scholar 

  • Chen HB, Huang HB (2005) Low temperature requirements for floral induction in lychee. Acta Hortic 665:195–202

    Google Scholar 

  • Coruzzi G, Zhou L (2001) Carbon and nitrogen sensing and signaling in plants: emerging ‘matrix effects’. Curr Opin Plant Sci 4:247–253

    Article  CAS  Google Scholar 

  • Dat J, Vandenbeele S, Vranova E, van Montagu M, Inzé D, van Breusegem F (2000) Dual action of the active oxygen species during plant stress responses. Cell Mol Life Sci 57:779–795

    Article  PubMed  CAS  Google Scholar 

  • Davenport TL, Stern RA (2005) Flowering. In: Menzel CM, Waite GK (eds) Litchi and longan. CABI, UK, pp 87–105

    Chapter  Google Scholar 

  • Diatchenko L, Lau YFC, Campbell AP, Chenchik A, Moqadam F, Huang B, Lukyanov S, Lukyanov K, Gurskaya N, Sverdlov ED, Siebert PD (1996) Suppression subtractive hybridization: a method for generating differentially regulated or tissue-specific cDNA probes and libraries. Proc Natl Acad Sci USA 93:6025–6030

    Article  PubMed  CAS  Google Scholar 

  • Dodge AD (1971) The mode of action of bipyridylium herbicides, paraquat and diquat. Endeavour 30:30–135

    Article  Google Scholar 

  • Finley D, Bartel B, Varshavsky A (1989) The tails of ubiquitin precursors are ribosomal proteins whose fusion to ubiquitin facilitates ribosome biogenesis. Nature 338:394–401

    Article  PubMed  CAS  Google Scholar 

  • Gibson S (2005) Control of plant development and gene expression by sugar sensing. Curr Opin Plant Biol 8:93–102

    Article  PubMed  CAS  Google Scholar 

  • Gulyani V, Khurana P (2011) Identification and expression profiling of drought-regulated genes in mulberry (Morus sp.) by suppression subtractive hybridization of susceptible and tolerant cultivars. Tree Genet Genomics 7:725–738

    Article  Google Scholar 

  • Hemerly AS, Ferreira P, de Almeida Engler J, van Montagu M, Engler G, Inzé D (1993) Cdc2a expression in Arabidopsis is linked with competence for cell division. Plant Cell Online 5:1711–1723

    CAS  Google Scholar 

  • Hobbie L (1998) Auxin: molecular genetic approaches in Arabidopsis. Plant Physiol Biochem 36:91–102

    Article  CAS  Google Scholar 

  • Huang HB, Chen HB (2005) A phase approach towards floral formation in lychee. Acta Hortic 665:185–194

    Google Scholar 

  • Inzé D, de Veylder L (2006) Cell cycle regulation in plant development. Annu Rev Genet 40:77–105

    Article  PubMed  Google Scholar 

  • Ito A, Hayama H, Kashimura Y (2002) Sugar metabolism in buds during flower bud formation: a comparison of two Japanese pear [Pyrus pyrifolia (Burm.) Nak.] cultivars possessing different flowering habits. Sci Hortic 96:163–175

    Article  CAS  Google Scholar 

  • Janssens V, Goris J (2001) Protein phosphatase 2A: a highly regulated family of serine/threonine phosphatases implicated in cell growth and signaling. Biochem J 353:417–439

    Article  PubMed  CAS  Google Scholar 

  • Kraus TE, Fletcher RA (1994) Paclobutrazol protects wheat seedlings from heat and paraquat injury. Is detoxification of active oxygen involved? Plant Cell Physiol 35:45–52

    CAS  Google Scholar 

  • Ku SJ, Park JY, Ha SB, Kim J (2009) Overexpression of IAA1 with domain II mutation impairs cell elongation and cell division in inflorescences and leaves of Arabidopsis. J Plant Physiol 166:548–553

    Article  PubMed  CAS  Google Scholar 

  • Liang W, Liang L, Ji Z, Li P (1987) The fluctuation of endogenous gibberellin and indole-3-acetic acid in Litchi chinensis shoot tips during floral initiation. Acta Hortic Sin 14:145–150

    Google Scholar 

  • Liu W (2012) Effects of sodium nitroprusside and paraquat on the litchi flowering and their related construction of SSH-cDNA libraries. Dissertation, South China Agricultural University

  • Lü J, Gao X, Dong Z, An L (2012) Expression of mitochondrial malate dehydrogenase in Escherichia coli improves phosphate solubilization. Ann Microbiol 62:607–614

    Article  Google Scholar 

  • Manochai P, Sruamsiri P, Wiriya-alongkorn W, Naphrom D, Hegele M, Bangerth F (2005) Year around off season flower induction in longan (Dimocarpus longan Lour.) trees by KClO3 applications: potentials and problems. Sci Hortic 104:379–390

    Article  CAS  Google Scholar 

  • Masura SS, Parveez GKA, Ismail I (2010) Isolation and characterization of oil palm constitutive promoter derived from ubiquitin extension protein (uep1) gene. New Biotechnol 27:289–299

    Article  CAS  Google Scholar 

  • Matsumoto TK (2006) Genes uniquely expressed in vegetative and potassium chlorate induced floral buds of Dimocarpus longan. Plant Sci 170:500–510

    Article  CAS  Google Scholar 

  • Menzel CM, Simpson DX (1988) Effect of temperature on growth and flowering of litchi (Litchi chinensis Sonn.) cultivars. J Hortic Sci 63:349–360

    CAS  Google Scholar 

  • Michaels SD (2009) Flowering time regulation produces much fruit. Curr Opin Plant Biol 12:75–80

    Article  PubMed  CAS  Google Scholar 

  • Nowack MK, Harashima H, Dissmeyer N, Zhao XA, Bouyer D, Weimer AK, De Winter F, Yang F, Schnittger A (2012) Genetic framework of cyclin-dependent kinase function in Arabidopsis. Dev Cell 22:1030–1040

    Article  PubMed  CAS  Google Scholar 

  • Nunez-Elisea R, Davenport TL (1994) Flowering of mango trees in containers as influenced by seasonal temperature and water stress. Sci Hortic 58:57–66

    Article  Google Scholar 

  • Park JY, Kim HJ, Kim J (2002) Mutation in domain II of IAA1 confers diverse auxin-related phenotypes and represses auxin-activated expression of Aux/IAA genes in steroid regulator-inducible system. Plant J 32:669–683

    Article  PubMed  CAS  Google Scholar 

  • Peng T, Zhu XF, Fan QJ, Sun PP, Liu JH (2012) Identification and characterization of low temperature stress responsive genes in Poncirus trifoliata by suppression subtractive hybridization. Gene 492:220–228

    Article  PubMed  CAS  Google Scholar 

  • Sauer M, Luschnig C, Wisniewska J, Reinohl V, Friml J, Benkova E (2006) Canalization of auxin flow by Aux/IAA-ARF-dependent feedback regulation of PIN polarity. Genes Dev 20:2902–2911

    Article  PubMed  CAS  Google Scholar 

  • Sheen J, Zhou L, Jang JC (1999) Sugars as signaling molecules. Curr Opin Plant Biol 2:410–418

    Article  PubMed  CAS  Google Scholar 

  • Vieten A, Vanneste S, Wisniewska J, Benkova E, Benjamins R, Beeckman T, Luschnig C, Friml J (2005) Functional redundancy of PIN proteins is accompanied by auxin-dependent cross-regulation of PIN expression. Development 132:4521–4531

    Article  PubMed  CAS  Google Scholar 

  • Wilkie JD, Sedgley M, Olesen T (2008) Regulation of floral initiation in horticultural trees. J Exp Bot 59:3215–3228

    Article  PubMed  CAS  Google Scholar 

  • Wisniewska J, Xu J, Seifertova D, Brewer PB, Ruzicka K, Blilou I, Rouquie D, Benkova E, Scheres B, Friml J (2006) Polar PIN localization directs auxin flow in plants. Science 312:883

    Article  PubMed  CAS  Google Scholar 

  • Zhang JZ, Ai XY, Sun LM, Zhang DL, Guo WW, Deng XX, Hu CG (2011) Molecular cloning and functional characterization of genes associated with flowering in citrus using an early-flowering trifoliate orange (Poncirus trifoliata L. Raf.) mutant. Plant Mol Biol 76:187–204

    Article  PubMed  CAS  Google Scholar 

  • Zhou JH, Pesacreta TC, Brown RC (1999) RNA isolation without gel formation from oligosaccharide rich onion epidermis. Plant Mol Bio Rep 17:397–407

    Article  CAS  Google Scholar 

  • Zhou B, Chen H, Huang X, Li N, Hu Z, Gao Z, Lu Y (2008) Rudimentary leaf abortion with the development of panicle in litchi: changes in ultrastructure, antioxidant enzymes and phytohormones. Sci Hortic 117:288–296

    Article  CAS  Google Scholar 

  • Zhou B, Chen H, Huang X, Wu G, Hu Z, Gao Z (2010) Changes of antioxidant enzyme activity and hydrogen peroxide concentration in Litchi chinensis during floral differentiation. Acta Hortic 863:453–460

    CAS  Google Scholar 

  • Zhou B, Li N, Zhang Z, Huang X, Chen H, Hu Z, Pang X, Liu W, Lu Y (2012) Hydrogen peroxide and nitric oxide promote reproductive growth in Litchi chinensis. Biol Plant 56:321–329

    Article  CAS  Google Scholar 

  • Zimmermann P, Heinlein C, Orendi G, Zentgraf U (2006) Senescence-specific regulation of catalases in Arabidopsis thaliana (L.) Heynh. Plant Cell Environ 29:1049–1060

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

We thank Md. Faruque Hossain for proofreading. This study was funded by the National Natural Science Foundation (31071760) and the Agricultural Industry Project (CARS-33-08) by the Ministry of Agriculture.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Bi-Yan Zhou.

Additional information

Communicated by J. Register.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Liu, WW., Kim, HJ., Chen, HB. et al. Identification of MV-generated ROS responsive EST clones in floral buds of Litchi chinensis Sonn.. Plant Cell Rep 32, 1361–1372 (2013). https://doi.org/10.1007/s00299-013-1448-8

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00299-013-1448-8

Keywords

Navigation