Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 55

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Physio-biochemical and molecular mechanism underlying the enhanced heavy metal tolerance in highland barley seedlings pre-treated with low-dose gamma irradiation

Wang, Xiaojie, Ma, Ruonan, Cui, Dongjie, Cao, Qing, Shan, Zhe, Jiao, Zhen·2017·Scientific Reports

Abstract

Heavy metal pollution, as a consequence of rapid industrialization and urbanization, poses a threat to highland barley grown in Tibet. This study investigates the effect of different doses of gamma irradiation (50–300 Gy) on the physio-biochemical and molecular mechanism of highland barley under heavy metal stress. Growth data showed that 50-Gy gamma irradiation had the maximal beneficial effects on the highland barley seedlings under lead/cadmium stress. The results of oxidative parameters demonstrated that 50-Gy gamma-irradiated seedlings had lower hydrogen peroxide and malondialdehyde contents under lead/cadmium stress compared to non-irradiated seedlings. Moreover, the activities of antioxidant enzyme and proline levels in 50-Gy gamma-irradiated seedlings were drastically higher than those in non-irradiated seedlings under lead/cadmium stress. Additionally, transmission electron microscopy results revealed that the 50-Gy gamma-irradiated seedlings exhibited improved chloroplasts ultrastructure compared with non-irradiated seedlings exposed to lead/cadmium stress. Notably, transcriptional expression analysis showed that 50-Gy gamma irradiation could significantly affect the expression of genes related to heavy metal transport and abscisic acid metabolism under lead/cadmium stress. Collectively, these results provide insights into the physio-biochemical and molecular mechanisms of low-dose-gamma-irradiation-enhanced heavy metal tolerance in highland barley seedlings, thus proposing gamma irradiation as a potential technology to mitigate heavy metal toxicity in crops.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1038/s41598-017-14601-8

Cites

1 of 1 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 1 references

Research works printed but not linked: 64

  1. Hassan, Z. & Aarts, M. G. M. Opportunities and feasibilities for biotechnological improvement of Zn, Cd or Ni tolerance and accumulation in plants. Environ. Exp. Bot. 72, 53–63 (2011). · DOI · Paper page
  2. Hong, B. S. et al. Understanding molecular mechanisms for improving phytoremediation of heavy metal-contaminated soils. Crit. Rev. Biotechnol. 30, 23–30 (2010). · DOI
  3. Puig, S., Andrés-Colás, N., García-Molina, A. & Peñarrubia, L. Copper and iron homeostasis in Arabidopsis: responses to metal deficiencies, interactions and biotechnological applications. Plant Cell Environ. 30, 271–290 (2007). · DOI · Paper page
  4. Uraguchi, S. & Fujiwara, T. Cadmium transport and tolerance in rice: perspectives for reducing grain cadmium accumulation. Rice. 5, 1–8 (2012). · DOI · Paper page
  5. Zheng, Y. Y., Duo, J., Cheng, S. B., Gao, S. B. & Dai, F. H. Progress in porphyry copper exploration from the Gangdise belt, Tibet, China. Front Earth Sci. 1, 226–232 (2007). · doi:10.1007/s11707-007-0028-z
  6. Fu, S., Chu, S. & Xu, X. Organochlorine pesticide residue in soils from Tibet, China. B. Environ. Contam. Tox. 66, 171–177 (2001). · doi:10.1007/s0012800221
  7. Xiao, C. D., Qin, D. H., Yao, T. D., Ren, J. W. & Li, Y. F. Spread of lead pollution over remote regions and upper troposphere: glaciochemical evidence from Polar Regions and Tibetan Plateau. B. Environ. Contam. Tox. 66, 691–698 (2001). · doi:10.1007/s001280064
  8. Huang, X., Sillanpää, M., Duo, B. & Gjessing, E. T. Water quality in the Tibetan Plateau: Metal contents of four selected rivers. Environ. Pollut. 156, 270–277 (2008). · doi:10.1016/j.envpol.2008.02.014
  9. Xie, H. T. et al. Assessment of Heavy Metal Contents in Surface Soil in the Lhasa–Shigatse–Nam Co Area of the Tibetan Plateau, China. B. Environ. Contam. Tox. 93, 192–198 (2014). · doi:10.1007/s00128-014-1288-4
  10. Huang, X., Sillanpää, M., Gjessing, E. T., Peräniemi, S. & Vogt, R. D. Environmental impact of mining activities on the surface water quality in Tibet: Gyama valley. Sci. Total Environ. 408, 4177–4184 (2010). · DOI
  11. Wang, J. et al. Speciation, distribution, and bioavailability of soil selenium in the Tibetan Plateau kashin-beck disease area-a case study in Songpan County, Sichuan Province, China. Biol. Trace Elem. Res. 156, 367–375 (2013). · DOI · Paper page
  12. Dai, F. et al. Tibet is one of the centers of domestication of cultivated barley. Proc. Natl. Acad. Sci. 109, 16969–16973 (2012). · DOI · Paper page
  13. Zhang, G. P., Wang, J. M. & Chen, J. X. Analysis of beta-glucan content in barley cultivars from different locations of China. Food Chem. 79, 251–254 (2002). · DOI
  14. Thapa, G., Sadhukhan, A., Panda, S. K. & Sahoo, L. Molecular mechanistic model of plant heavy metal tolerance. Biometals. 25, 489–505 (2012). · DOI
  15. Sandalio, L. M., Dalurzo, H. C., Gómez, M., Romero-Puertas, M. C. & Del Río, L. A. Cadmium-induced changes in the growth and oxidative metabolism of pea plants. J. Exp. Bot. 52, 2115–2126 (2001). · DOI · Paper page
  16. Ortega–Villasante, C., Rellán-Álvarez, R., Del Campo, F. F., Carpena-Ruiz, R. O. & Hernández, L. E. Cellular damage induced by cadmium and mercury in Medicago sativa. J. Exp. Bot. 56, 2239–2251 (2005). · DOI · Paper page
  17. Raghavendra, A. S., Gonugunta, V. K., Christmann, A. & Grill, E. ABA perception and signalling. Trends Plant Sci. 15, 395–401 (2010). · DOI · Paper page
  18. Seiler, C. et al. ABA biosynthesis and degradation contributing to ABA homeostasis during barley seed development under control and terminal drought-stress conditions. J. Exp. Bot. 62, 2615–2632 (2011). · DOI · Paper page
  19. Gill, S. S. & Tuteja, N. Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol. Biochem. 48, 909–930 (2010). · DOI · Paper page
  20. Moussa, H. R. Role of gamma irradiation in regulation of NO3 level in rocket (Eruca vesicaria subsp. sativa) plants. Russ. J. Plant Physiol. 53, 193–197 (2006). · DOI
  21. Bala, M. & Singh, K. P. Mutagenesis of rose (L.) explants using gamma-radiation to induce novel flower colour mutations. J. Horti. Sci. Biotech. 88, 462–468 (2013). · doi:10.1080/14620316.2013.11512992
  22. He, S., Han, Y., Wang, Y., Zhai, H. & Liu, Q. In vitro selection and identification of sweetpotato (Ipomoea batatas (L.) Lam.) plants tolerant to NaCl. Plant Cell, Tiss. Org. 96, 69–74 (2009). · DOI
  23. Jamil, M. & Khan, U. Q. Study of genetic variation in yield components of wheat cultivar bukhtwar-92 as induced by gamma radiation. Asian J. Plant Sci. 1, 579–580 (2002). · doi:10.3923/ajps.2002.579.580
  24. Melki, M. & Dahmani, T. Gamma Irradiation Effects on Durum Wheat (Triticum durum Desf.) under Various Conditions. Pak. J. Biol. Sci. 12, 1531–1534 (2009). · doi:10.3923/pjbs.2009.1531.1534
  25. Macovei, A. et al. Synergistic exposure of rice seeds to different doses of γ-ray and salinity stress resulted in increased antioxidant enzyme activities and genespecific modulation of TC-NER pathway. Biomed Res. Int. 676934, 15 (2014).
  26. Moussa, H. R. Low dose of gamma irradiation enhanced drought tolerance in soybean. Bulg. J. Agric. Sci. 17, 63–72 (2011).
  27. Mohammed, A. H., Mohamed, H. I., Zaki, L. M. & Mogazy, A. M. Pre-exposure to gamma rays alleviates the harmful effect of salinity on cowpea plants. J. Stress Physiol. Biochem. 8, 199–217 (2012).
  28. Abo-Hamad, S. A. E. H., Allah, K. M. G. S. & Abo-Kassem, E. E. D. M. Effect of gamma irradiation or potassium on some primary and secondary metabolites of Brassica rapa (L.) root under cadmium stress. Int. Res. J. Agr. Sci. Soil Sci. 3, 408–415 (2013).
  29. Qi, W. C. et al. Pretreatment with low-dose gamma irradiation enhances tolerance to the stress of cadmium and lead in Arabidopsis thaliana seedlings. Ecotoxicol. Environ. Saf. 115, 243–249 (2015). · DOI
  30. Mostofa, M. G. et al. Hydrogen sulfide modulates cadmium-induced physiological and biochemical responses to alleviate cadmium toxicity in rice. Sci. Rep. 5, 14078 (2015). · DOI · Paper page
  31. Mittler, R. Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci. 7, 405–410 (2002). · DOI · Paper page
  32. Qi, W. C., Zhang, L., Xu, H. B., Wang, L. & Jiao, Z. Physiological and molecular characterization of the enhanced salt tolerance induced by low-dose gamma irradiation in Arabidopsis seedlings. Biochem Biophys Res Commun. 450, 1010–1015 (2014). · doi:10.1016/j.bbrc.2014.06.086
  33. Marcu, D., Cristea, V. & Daraban, L. Dose-dependent effects of gamma radiation on lettuce (Lactuca sativa var. capitata) seedlings. Int. J. Radiat. Biol. 89, 219–223 (2013). · doi:10.3109/09553002.2013.734946
  34. Melki, M. & Sallami, D. Studies the effects of low dose of gamma rays on the behaviour of chickpea under various conditions. Pak. J. Biol. Sci. 11, 2326–2330 (2008). · doi:10.3923/pjbs.2008.2326.2330
  35. Maity, J. P., Mishra, D. & Chakraborty, A. Modulation of some quantitative and qualitative characteristics in rice (Oryza sativa L.) and mung (Phaseolus mungo L.) by ionizing radiation. Radiat. Phys. Chem. 74, 391–394 (2005). · doi:10.1016/j.radphyschem.2004.08.005
  36. Bhosale, U. P. & Hallale, B. V. Gamma Radiation Induced Mutations in Black gram (Vigna mungo (L.) Hepper). Asian J. Plant Sci. Res. 1, 96–100 (2011).
  37. Hegazi, A. Z. & Hamideldin, N. The effect of gamma irradiation on enhancement of growth and seed yield of okra [Abelmoschus esculentus (L.) Monech] and associated molecular changes. Journal of Horticulture and Forestry. 2, 38–51 (2010).
  38. Marcu, D., Damian, G., Cosma, C. & Cristea, V. Gamma radiation effects on seed germination, growth and pigment content, and ESR study of induced free radicals in maize (Zea mays). J. Biol. Phys. 39, 625–634 (2013). · doi:10.1007/s10867-013-9322-z
  39. Akshatha Chandrashekar, K. R., Somashekarappa, H. M. & Souframanien, J. Effect of gamma irradiation on germination, growth, and biochemical parameters of Terminalia arjuna Roxb. Radiation Protection and Environment 36, 38–44 (2014). · doi:10.4103/0972-0464.121826
  40. Beyaz, R., Kahramanogullari, C. T., Yildiz, C., Darcin, E. S. & Yildiz, M. The effect of gamma radiation on seed germination and seedling growth of Lathyrus chrysanthus Boiss. under invitro conditions. J. Environ. Radioactiv. 162–163, 129–133 (2016). · doi:10.1016/j.jenvrad.2016.05.006
  41. Kuzin, A. M., Vagabova, M. E. & Revin, A. F. Molecular mechanisms of the stimulating action of ionizing radiation on seeds part 2 activation of protein and high molecular rna synthesis. Radiobiology. 16, 259–261 (1976).
  42. Kovalchuk, I., Molinier, J., Yao, Y., Arkhipov, A. & Kovalchuk, O. Transcriptome analysis reveals fundamental differences in plant response to acute and chronic exposure to ionizing radiation. Mutat. Res. 624, 101–113 (2007). · DOI
  43. Kim, D. S. et al. Antioxidant response of Arabidopsis plants to gamma irradiation: genome-wide expression profiling of the ROS scavenging and signal transduction pathways. J. Plant Physiol. 168, 1960–1971 (2011). · DOI
  44. Fan, X., Toivonen, P. M. A., Rajkowski, K. T. & Sokorai, K. J. B. Warm water treatment in combination with modified atmosphere packaging reduces undesirable effects of irradiation on the quality of fresh-cut iceberg lettuce. J. Agr. Food Chem. 51, 1231–1236 (2003). · doi:10.1021/jf020600c
  45. Hameed, A., Shah, T. M., Atta, M. B., Haq, M. A. & Sayed, H. Gamma irradiation effects on seed germination and growth, protein content, peroxidase and protease activity, lipid peroxidation in desi and kabuli chickpea. Pak. J. Bot. 40, 1033–1041 (2008).
  46. Mittler, R., Vanderauwera, S., Gollery, M. & Breusegem, F. V. Reactive oxygen gene network of plants. Trends Plant Sci. 9, 490–498 (2004). · DOI · Paper page
  47. Arora, A., Sairam, R. K. & Srivastava, G. C. Oxidative stress and antioxidative system in plants. Curr. Sci. Association. 82, 1227–1238 (2002).
  48. Wi, S. G. et al. Effects of gamma irradiation on morphological changes and biological responses in plants. Micron. 38, 553–564 (2007). · DOI · Paper page
  49. Esnault, M. A., Legue, F. & Chenal, C. Ionizing radiation: Advances in plant response. Environ. Exp. Bot. 68, 231–237 (2010). · DOI · Paper page
  50. Ashraf, M. & Foolad, M. R. Roles of glycinebetaine and proline in improving plant abiotic stress resistance. Environ. Exp. Bot. 59, 206–216 (2007). · DOI · Paper page
  51. Islam, M. M. et al. Exogenous proline and glycinebetaine increase antioxidant enzyme activities and confer tolerance to cadmium stress in cultured tobacco cells. J. Plant Physiol. 166, 1587–1597 (2009). · DOI · Paper page
  52. Abo-Hamad, S. A. E. H., Allah, K. M. G. S. & Abo-Kassem, E. E. D. M. Effect of gamma irradiation or potassium on some primary and secondary metabolites of Brassica rapa (L.) root under cadmium stress. Int. Res. J. Agric. Sci. Soil Sci. 3, 408–415 (2013).
  53. Virgin, H. I. 1–The Chloroplast as Site of Chlorophyll Formation and Photosynthesis: A Short History. Pigment–protein Complexes in Plastids. 1–23 (1993). · doi:10.1016/b978-0-12-676960-9.50006-7
  54. Hou, W. H., Chen, X., Song, G. L., Wang, Q. H. & Chang, C. C. Effects of copper and cadmium on heavy metal polluted waterbody restoration by duckweed (Lemna minor). Plant Physiol. Bioch. 45, 62–69 (2007). · DOI
  55. Singh, V. P. Toxic metal cadmium: phytotoxicity and tolerance in plants, In R. K. Trivedy (Ed.). Adv. Environ. Sci. Tech. 225–256 (1995).
  56. Matsuoka, M. & Igisu, H. Effects of Heavy Metals on Mitogen-Activated protein kinase pathways. Environ. Health Prev. Medicine. 6, 210–217 (2002). · DOI
  57. Qi, W. C. et al. ROS and ABA signaling are involved in the growth stimulation induced by low-dose gamma irradiation in Arabidopsis seedling. Appl Biochem Biotechnol. 175, 1490–1506 (2015). · doi:10.1007/s12010-014-1372-6
  58. Patterson, B. D., MacRae, E. A. & Ferguson, I. B. Estimation of hydrogen peroxide in plant extracts using titanium(IV). Anal. Biochem. 139, 487–492 (1984). · DOI · Paper page
  59. Shalata, A. & Neumann, P. M. Exogenous ascorbic acid (vitamin C) increases resistance to salt stress and reduces lipid peroxidation. J. Exp. Bot. 52, 2207–2211 (2001). · DOI · Paper page
  60. Giannopolitis, C. N. & Ries, S. K. Superoxide dismutases: I. Occurrence in higher plants. Plant Physiol. 59, 309–314 (1977). · DOI · Paper page
  61. Bergmeyer, N. Methoden der enzymatischen Analyse. Akademie-Verlag, Berlin (1970). · DOI
  62. Zhang, J. & Kirkham, M. B. Drought-stress-induced changes in activities of superoxide dismutase, catalase, and peroxidase in wheat species. Plant Cell Physiol. 35, 785–791 (1994). · DOI · Paper page
  63. Bates, L. S., Waldren, R. P. & Teare, I. D. Rapid determination of free proline for water-stress studies. Plant Soil. 39, 205–207 (1973). · DOI · Paper page
  64. Schmittgen, T. D. & Livak, K. J. Analyzing real-time PCR data by the comparative C(T) method. Nat. Protoc. 3, 1101–1108 (2008). · DOI · Paper page

Cited by

See all 55

Metadata

Authors
Wang, X., Ma, R., Cui, D., Cao, Q., Shan, Z., & Jiao, Z.
Venue
Scientific Reports
Published
2017-10-27
Volume
7
Issue
1
ISSN
2045-2322
Cited by
55
References
1
Language
en
Licence

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: Physio-biochemical and molecular mechanism underlying the enhanced heavy metal tolerance in highland barley seedlings pre-treated with low-dose gamma irradiation. https://app.cochat.ai/papers/10.1038/s41598-017-14601-8
The paper
Wang, X., Ma, R., Cui, D., Cao, Q., Shan, Z., & Jiao, Z. (2017). Physio-biochemical and molecular mechanism underlying the enhanced heavy metal tolerance in highland barley seedlings pre-treated with low-dose gamma irradiation. Scientific Reports. https://doi.org/10.1038/s41598-017-14601-8

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.