Skip to main content

Advertisement

Log in

The dehydrin gene of the Arctic plant Cerastium arcticum, CaDHN, increases tolerance to multiple stresses in Arabidopsis thaliana

  • Original Article
  • Published:
Plant Biotechnology Reports Aims and scope Submit manuscript

Abstract

Cerastium arcticum is one of the few flowering plants that thrives in the Arctic, suggesting that it possesses mechanisms for overcoming this extreme environment. To verify the functionality of C. arcticum dehydrin (CaDHN), known to play a protective role during cellular dehydration, the gene was introduced to Arabidopsis and Escherichia coli. Transgenic plants expressing CaDHN had significantly greater fresh weight and relative water content than wild-type plants under 15% PEG treatments, representing enhanced tolerance to drought. Under chilling conditions, transgenic plants remained vivid green, containing about 1.35-fold higher levels of chlorophyll than wild-type plants, and transgenic seeds germinated 2–3 days earlier with approximately threefold higher germination rates than wild-type seeds. Furthermore, oxidative stress under chilling conditions was 30% lower in transgenic plants than in wild-type plants. Transgenic plants also showed improved tolerance to various stresses, such as cold shock and salinity. In addition, transformed E. coli expressing CaDHN also showed enhanced tolerance to stress conditions, which suggests that CaDHN is conserved across taxa to provide tolerance to stress. These results indicate that CaDHN plays an important role in conferring tolerance to oxidative stress.

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

  • Allagulova CR, Gimalov F, Shakirova F, Vakhitov V (2003) The plant dehydrins: structure and putative functions. Biochemistry (Moscow) 68:945–951

    Article  CAS  Google Scholar 

  • Archambault A, Strömvik MV (2011) PR-10, defensin and cold dehydrin genes are among those over expressed in Oxytropis (Fabaceae) species adapted to the arctic. Funct Integr Genomics 11:497–505

    Article  CAS  Google Scholar 

  • Artus NN, Uemura M, Steponkus PL, Gilmour SJ, Lin C, Thomashow MF (1996) Constitutive expression of the cold-regulated Arabidopsis thaliana COR15a gene affects both chloroplast and protoplast freezing tolerance. Proc Natl Acad Sci 93:13404–13409

    Article  CAS  Google Scholar 

  • Battaglia M, Olvera-Carrillo Y, Garciarrubio A, Campos F, Covarrubias AA (2008) The enigmatic LEA proteins and other hydrophilins. Plant Physiol 148:6–24

    Article  CAS  Google Scholar 

  • Bokhorst S, Bjerke J, Bowles F, Melillo J, Callaghan T, Phoenix G (2008) Impacts of extreme winter warming in the sub-Arctic: growing season responses of dwarf shrub heathland. Glob Change Biol 14:2603–2612

    Google Scholar 

  • Brett OE (1953) Cerastium arcticum Lange. Nature 171:527–528

    Article  Google Scholar 

  • Brini F, Hanin M, Lumbreras V, Amara I, Khoudi H, Hassairi A, Pages M, Masmoudi K (2007) Overexpression of wheat dehydrin DHN-5 enhances tolerance to salt and osmotic stress in Arabidopsis thaliana. Plant Cell Rep 26:2017–2026

    Article  CAS  Google Scholar 

  • Campbell SA, Close TJ (1997) Dehydrins: genes, proteins, and associations with phenotypic traits. New Phytol 137:61–74

    Article  CAS  Google Scholar 

  • Cellier F, Conéjéro G, Breitler J-C, Casse F (1998) Molecular and physiological responses to water deficit in drought-tolerant and drought-sensitive lines of sunflower: accumulation of dehydrin transcripts correlates with tolerance. Plant Physiol 116:319–328

    Article  CAS  Google Scholar 

  • Chew O, Lelean S, John UP, Spangenberg GC (2012) Cold acclimation induces rapid and dynamic changes in freeze tolerance mechanisms in the cryophile Deschampsia antarctica E. Desv. Plant Cell Environ 35:829–837

    Article  CAS  Google Scholar 

  • Close TJ (1997) Dehydrins: a commonalty in the response of plants to dehydration and low temperature. Physiol Plant 100:291–296

    Article  CAS  Google Scholar 

  • Desikan R, Neill SJ, Hancock JT (2000) Hydrogen peroxide-induced gene expression in Arabidopsis thaliana. Free Radic Biol Med 28:773–778

    Article  CAS  Google Scholar 

  • Drira M, Saibi W, Amara I, Masmoudi K, Hanin M, Brini F (2015) Wheat dehydrin K-segments ensure bacterial stress tolerance, antiaggregation and antimicrobial effects. Appl Biochem Biotechnol 175:3310–3321

    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 

  • Hagen AR, Giese H, Brochmann C (2001) Trans-Atlantic dispersal and phylogeography of Cerastium arcticum (Caryophyllaceae) inferred from RAPD and SCAR markers. Am J Bot 88:103–112

    Article  CAS  Google Scholar 

  • Halder T, Upadhyaya G, Basak C, Das A, Chakraborty C, Ray S (2018) Dehydrins impart protection against oxidative stress in transgenic tobacco plants. Front Plant Sci 9:136

    Article  Google Scholar 

  • Hanin M, Brini F, Ebel C, Toda Y, Takeda S, Masmoudi K (2011) Plant dehydrins and stress tolerance: versatile proteins for complex mechanisms. Plant Signal Behav 6:1503–1509

    Article  CAS  Google Scholar 

  • Hara M, Fujinaga M, Kuboi T (2004) Radical scavenging activity and oxidative modification of citrus dehydrin. Plant Physiol Biochem 42:657–662

    Article  CAS  Google Scholar 

  • Hara M, Fujinaga M, Kuboi T (2005) Metal binding by citrus dehydrin with histidine-rich domains. J Exp Bot 56:2695–2703

    Article  CAS  Google Scholar 

  • Hara M, Kondo M, Kato T (2013) A KS-type dehydrin and its related domains reduce Cu-promoted radical generation and the histidine residues contribute to the radical-reducing activities. J Exp Bot 64:1615–1624

    Article  CAS  Google Scholar 

  • Hara M, Monna S, Murata T, Nakano T, Amano S, Nachbar M, Wätzig H (2016) The Arabidopsis KS-type dehydrin recovers lactate dehydrogenase activity inhibited by copper with the contribution of His residues. Plant Sci 245:135–142

    Article  CAS  Google Scholar 

  • Kim I-S, Kim H-Y, Kim Y-S, Choi H-G, Kang S-H, Yoon H-S (2013) Expression of dehydrin gene from Arctic Cerastium arcticum increases abiotic stress tolerance and enhances the fermentation capacity of a genetically engineered Saccharomyces cerevisiae laboratory strain. Appl Microbiol Biotechnol 97:8997–9009

    Article  CAS  Google Scholar 

  • Liu Y, Liang J, Sun L, Yang X, Li D (2016) Group 3 LEA protein, ZmLEA3, is involved in protection from low temperature stress. Front Plant Sci 7:1011

    PubMed  PubMed Central  Google Scholar 

  • Liu Y, Song Q, Li D, Yang X, Li D (2017) Multifunctional roles of plant dehydrins in response to environmental stresses. Front Plant Sci 8:1018

    Article  Google Scholar 

  • Lopez CG, Banowetz GM, Peterson CJ, Kronstad WE (2003) Dehydrin expression and drought tolerance in seven wheat cultivars. Crop Sci 43:577–582

    Article  CAS  Google Scholar 

  • Moon S-J, Min MK, Kim J, Kim DY, Yoon IS, Kwon TR, Byun MO, Kim B-G (2019) Ectopic expression of OsDREB1G, a member of the OsDREB1 subfamily, confers cold stress tolerance in rice. Front Plant Sci 10:297

    Article  Google Scholar 

  • Murashige T, Skoog F (1962) A revised medium for rapid growth and bio assays with tobacco tissue cultures. Physiol Plant 15:473–497

    Article  CAS  Google Scholar 

  • Olave-Concha N, Ruiz-Lara S, Munoz X, Bravo LA, Corcuera LJ (2004) Accumulation of dehydrin transcripts and proteins in response to abiotic stresses in Deschampsia antarctica. Antarct Sci 16:175–184

    Article  Google Scholar 

  • Orozco-Cárdenas ML, Narváez-Vásquez J, Ryan CA (2001) Hydrogen peroxide acts as a second messenger for the induction of defense genes in tomato plants in response to wounding, systemin, and methyl jasmonate. Plant Cell 13:179–191

    Article  Google Scholar 

  • Puhakainen T, Hess MW, Mäkelä P, Svensson J, Heino P, Palva ET (2004) Overexpression of multiple dehydrin genes enhances tolerance to freezing stress in Arabidopsis. Plant Mol Biol 54:743–753

    Article  CAS  Google Scholar 

  • Rorat T (2006) Plant dehydrins—tissue location, structure and function. Cell Mol Biol Lett 11:536

    Article  CAS  Google Scholar 

  • Shekhawat UKS, Srinivas L, Ganapathi TR (2011) MusaDHN-1, a novel multiple stress-inducible SK3-type dehydrin gene, contributes affirmatively to drought-and salt-stress tolerance in banana. Planta 234:915

    Article  CAS  Google Scholar 

  • Shultz RW, Settlage SB, Hanley-Bowdoin L, Thompson WF (2005) A trichloroacetic acid-acetone method greatly reduces infrared autofluorescence of protein extracts from plant tissue. Plant Mol Biol Rep 23:405–409

    Article  CAS  Google Scholar 

  • Tjokrokusumo D, Heinrich T, Wylie S, Potter R, McComb J (2000) Vacuum infiltration of Petunia hybrida pollen with Agrobacterium tumefaciens to achieve plant transformation. Plant Cell Rep 19:792–797

    Article  CAS  Google Scholar 

  • Wolff SP (1994) [18]Ferrous ion oxidation in presence of ferric ion indicator xylenol orange for measurement of hydroperoxides. Methods in enzymology. Elsevier, Amsterdam, pp 182–189

    Google Scholar 

Download references

Funding

This research was supported by Kyungpook National University Research Fund 2017.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Ho-Sung Yoon.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary file1 (DOCX 1962 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Shin, SY., Kim, HY., Kim, IS. et al. The dehydrin gene of the Arctic plant Cerastium arcticum, CaDHN, increases tolerance to multiple stresses in Arabidopsis thaliana. Plant Biotechnol Rep 14, 387–395 (2020). https://doi.org/10.1007/s11816-020-00611-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11816-020-00611-y

Keywords

Navigation