Skip to main content
Log in

Proline accumulation and related gene expression during spring regrowth in three rosaceae species

  • Research Report
  • Published:
Horticulture, Environment, and Biotechnology Aims and scope Submit manuscript

Abstract

Proline (Pro), one of amino acids, not only acts as an osmoprotectant but also is involved in plant developmental processes. We previously revealed that Pro levels increased in peach (Prunus persica) shoots during dehardening in response to warmer temperatures during spring or in controlled laboratory conditions. Our subsequent work suggested that such Pro accumulation is associated with the resumption of growth in eco-dormant shoots and mediated via the ornithine pathway in peach. The present study was conducted to explore whether the aforementioned Pro accumulation response also occurs in other species of the Rosaceae family. Our data indicate that the Pro content of peach and plum (P. salicina) shoots increased during the spring regrowth and were highly similar between these two related species. Whereas the ornithine-δ-aminotransferase (OAT) gene expression dynamics in peach were correlated with Pro accumulation pattern and with pyrroline-5-carboxylate reductase (P5CR) gene expression, OAT expression was not correlated with the Pro content in plum. For apple (Malus domestica), while the absolute amounts of Pro content differed from those of the two Prunus species, this species accumulated Pro during the spring warming/regrowth. These results suggest that Pro accumulation in response to higher temperatures during the spring regrowth is a more general phenomenon across Rosaceae fruit trees, and although peach shoots may accumulate Pro via the ornithine pathway during spring regrowth, there was no evidence for this in plum and apple.

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.

Similar content being viewed by others

Literature Cited

  • Armengaud P, Thiery L, Buhot N, March GG, Savouré A (2004) Transcriptional regulation of proline biosynthesis in Medicago truncatula reveals developmental and environmental specific features. Physiol Plant 120: 422–450

    Article  Google Scholar 

  • Arora R, Wisniewski ME, Scorza R (1992) Cold acclimation in genetically related (sibling) deciduous and evergreen peach (Prunus persica [L.] Batsch). I. Seasonal changes in cold hardiness and polypeptides of bark and xylem tissue. Plant Physiol 99: 1562–1568

    CAS  PubMed  Google Scholar 

  • Bagdi DL, Shaw BP (2013) Analysis of proline metabolic enzymes in Oryza sativa under NaCl stress. J Environ Biol 34: 677–681

    CAS  PubMed  Google Scholar 

  • Bates LS, Waldren RP, Teare ID (1973) Rapid determination of free proline for water-stress studies. Plant Soil 39: 205–207

    Article  CAS  Google Scholar 

  • Chiang HH, Dandekar AM (1995) Regulation of proline accumulation in Arabidopsis thaliana (L.) Heynh during development and in response to desiccation. Plant Cell Environ 18: 1280–1290

    Article  CAS  Google Scholar 

  • Chu TM, Aspinall D, Paleg LG (1974) Stress metabolism. VI. Temperature stress and the accumulation of proline in barley and radish. Aust J Plant Physiol 1: 87–97

    CAS  Google Scholar 

  • Delauney AJ, Hu CAA, Kavi Kishor PB, Verma DPS (1993) Cloning of ornithine d-aminotransferase cDNA from Vigna aconitifolia by trans-complementation in Escherichia coli and regulation of proline biosynthesis. J Biol Chem 268: 18673–18678

    CAS  PubMed  Google Scholar 

  • Duncan DR, Widholm JM (1987) Proline accumulation and its implication in cold tolerance of regenerable maize callus. Plant Physiol 83: 703–708

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Elthon TE, Stewart CR (1982) Proline oxidation in corn mitochondria. Plant Physiol 70: 567–572

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Handa S, Handa AK, Hasegawa PM, Bressan RA (1986) Proline accumulation and the adaptation of cultured plant cells to water stress. Plant Physiol 80: 938–945

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Hur J, Jung KH, Lee CH, An G (2004) Stress-inducible OsP5CS2 gene is essential for salt and cold tolerance in rice. Plant Sci 167: 417–426

    Article  CAS  Google Scholar 

  • Kavi Kishor PB, Sreenivasulu N (2014) Is proline accumulation per se correlated with stress tolerance or is proline homeostasis a more critical issue? Plant Cell Environ 37: 300–311

    Article  CAS  PubMed  Google Scholar 

  • Khalafalla MS, Palzkill DA (1990) Seasonal patterns of carbohydrates and proline in jojoba clones that differ in frost susceptibility. Hortic Sci 25: 103–105

    CAS  Google Scholar 

  • Kushad MM, Yelenosky G (1987) Evaluation of polyamine and proline levels during low temperature acclimation of citrus. Plant Physiol 84: 692–695

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Lee TM, Chang YC (1999) An increase of ornithine d-aminotransferasemediated proline synthesis in relation to high-temperature injury in Gracilaria tenuistipitata (Gigartinales, Rhodophyta). J Phycol 35: 84–88

    Article  Google Scholar 

  • Lehmann S, Funck D, Szabados L, Rentsch D (2010) Proline metabolism and transport in plant development. Amino Acids 39: 949–962

    Article  CAS  PubMed  Google Scholar 

  • Lutts S, Majerus V, Kinet JM (1999) NaCl effects on proline metabolism in rice (Oryza sativa) seedlings. Physiol Plant 105: 450–458

    Article  CAS  Google Scholar 

  • Nanjo T, Kobayashi M, Yoshiba Y, Sanada Y, Wada K, Tsukaya H, Kakubari H, Yamagushi-Shinozaki K, Shinozaki K (1999) Biological functions of proline in morphogenesis and osmotolerance revealed in antisense transgenic Arabidopsis thaliana. Plant J 18: 185–193

    Article  CAS  PubMed  Google Scholar 

  • Patton AJ, Cunningham SM, Volence JJ, Reicher ZJ (2007) Differences in freeze tolerance of zoysiagrasses: II. Carbohydrate and proline accumulation. Crop Sci 47: 2170–2181

    CAS  Google Scholar 

  • Rocha IMA, Vitorello VA, Silva JS, Ferreira-Silva SL, Viégas RA, Silva EN, Silveira JAG (2012) Exogenous ornithine is an effective precursor and the d-ornithine amino transferase pathway contributes to proline accumulation under high N recycling in salt-stressed cashew leaves. J Plant Physiol 169: 41–49

    Article  PubMed  Google Scholar 

  • Roosens NH, Thu TT, Iskandar HM, Jacobs M (1998) Isolation of the ornithine-delta-aminotransferase cDNA and effect of salt stress on its expression in Arabidopsis thaliana. Plant Physiol 117: 263–271

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Savouré A, Hua XJ, Bertauche N, van Montagu M, Verbruggen N (1997) Abscisic acid-independent and abscisic acid-dependent regulation of proline biosynthesis following cold and osmotic stresses in Arabidopsis thaliana. Mol Gen Genet 254: 104–109

    Article  PubMed  Google Scholar 

  • Schwacke R, Grallath S, Breitkrewz KE, Stransky H, Frommer WB, Rentsch D (1999) LeProT1, a transporter for proline, glycine betaine, and amino butyric acid in tomato pollen. Plant Cell 11: 337–391

    Google Scholar 

  • Shin H, Kim K, Oh Y, Yun SK, Oh SI, Sung J, Kim D (2015a) Carbohydrate changes in peach shoot tissues and their relationship to cold acclimation and deacclimation. Horticult J 84: 24–29

    Article  Google Scholar 

  • Shin H, Oh S, Arora R, Kim D (2016a) Proline accumulation in response to high temperature in winter-acclimated shoots of Prunus persica: a response associated with growth resumption or heat stress? Can J Plant Sci 96: 630–638

    Article  Google Scholar 

  • Shin H, Oh S, Kim K, Kim D (2016b) Proline accumulates in response to higher temperatures during dehardening in peach shoot tissues. Horticult J 85: 37–45

    Article  Google Scholar 

  • Shin H, Oh SI, Kim MA, Yun SK, Oh Y, Son IC, Kim HS, Kim D (2015b) Relationship between cold hardiness and dehydrin gene expression in peach shoot tissues under field conditions. Hortic Environ Biotechnol 56: 280–287

    Article  CAS  Google Scholar 

  • Shin H, Oh Y, Kim D (2015c) Differences in cold hardiness, carbohydrates, dehydrins and related gene expressions under an experimental deacclimation and reacclimation in Prunus persica. Physiol Plant 154: 485–499

    Article  CAS  PubMed  Google Scholar 

  • Smirnoff N, Cumbes QJ (1989) Hydroxyl radical scavenging activity of compatible solutes. Phytochemistry 28: 1057–1060

    Article  CAS  Google Scholar 

  • Szabados L, Savouré A (2010) Proline: a multifunctional amino acid. Trends Plant Sci 15: 89–97

    Article  CAS  PubMed  Google Scholar 

  • Tong Z, Gao Z, Wang F, Zhou J, Zhang Z (2009) Selection of reliable reference genes for gene expression studies in peach using real-time PCR. BMC Mol Biol 10: 71–83

    Article  PubMed  PubMed Central  Google Scholar 

  • Xue X, Liu A, Hua X (2009) Proline accumulation and transcriptional regulation of proline biosynthesis and degradation in Brassica napus. BMB Rep 42: 28–34

    Article  CAS  PubMed  Google Scholar 

  • Yelenosky G (1979) Accumulation of free proline in citrus leaves during cold hardening of young trees in controlled temperature regimes. Plant Physiol 64: 425–427

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Yoshiba Y, Kiyosue T, Nakashima K, Yamaguchi-Shinozaki K, Shinozaki K (1997) Regulation of levels of proline as an osmolyte in plants under water stress. Plant Cell Physiol 38: 1095–1102

    Article  CAS  PubMed  Google Scholar 

  • Zhang X, Wang K, Ervin EH, Waltz C, Murphy T (2011) Metabolic changes during cold acclimation and deacclimation in five bermudagrass varieties. I. Proline, total amino acid, protein, and dehydrin expression. Crop Sci 51: 838–846

    CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Daeil Kim.

Additional information

These authors contributed equally to this work.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Oh, S., Shin, H., Arora, R. et al. Proline accumulation and related gene expression during spring regrowth in three rosaceae species. Hortic. Environ. Biotechnol. 58, 21–26 (2017). https://doi.org/10.1007/s13580-017-0101-9

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s13580-017-0101-9

Additional key words

Navigation