PLANT BIOLOGY
ANIMAL BIOLOGY
SUBSCRIPTION
E-SUBSCRIPTION
 
MAP
MAIN PAGE

 

 

 

 

doi: 10.15389/agrobiology.2025.3.432eng

UDC: 633.111.1:632.112

Acknowledgements:
Supported financially by the grant of the Russian Science Foundation (project No. 23-26-00246, https://rscf.ru/project/23-26-00246/)

 

THE ROLE OF HORMONAL SYSTEM AND LECTIN IN THE PROTECTIVE EFFECT OF 24-EPIBRASSINOLIDE ON WHEAT (Triticum aestivum L.) SEEDLINGS DIFFERING IN DROUGHT ADAPTATION STRATEGIES UNDER WATER DEFICIT

A.M. Avalbaev, R.A. Yuldashev, Ch.R. Allagulova,
A.A. Plotnikov, O.V. Lastochkina

Institute of Biochemistry and Genetics — Subdivision of the Ufa Federal Research Center RAS, 71, pr. Oktyabrya, Ufa, Russia 450054, e-mail avalbaev@yahoo.com (✉ corresponding author),yuldashevra@gmail.com,
allagulova-chulpan@rambler.ru,plotnikow87@mail.ru,
oksana.lastochkina@ufaras.ru

ORCID:
Avalbaev A.M. orcid.org/0000-0002-4001-0700
Plotnikov A.A. orcid.org/0009-0006-2968-2262
Yuldashev R.A. orcid.org/0000-0001-9033-6867
Lastochkina O.V. orcid.org/0000-0003-3398-1493
Allagulova Ch.R. orcid.org/0000-0002-7547-8215

Final revision received October 01, 2024
Accepted November 28, 2024

A major challenge of modern plant science is unravelling the mechanisms of plant tolerance to drought which leads to disruption of all metabolic events and loss of productivity of plants. Two ecologo-geographical groups (ecotypes) of wheat have formed in the Russian Federation, which differ significantly in their adaptation strategies to drought — the forest-steppe West Siberian and steppe Volga ecotypes. The differences between ecotypes are especially characteristic in the initial stage of ontogenesis. The cultivars of the forest-steppe West Siberian ecotype are characterized by delayed germination and seedling growth. In contrast, seedlings of the steppe Volga ecotype develop rapidly and are more tolerant in comparison with plants of the forest-steppe West Siberian ecotype in the early stage of development. Growth regulators play an important role in regulation of drought tolerance in plants. There has been increasing amount of data demonstrating the involvement of steroidal phytohormones brassinosteroids, characterized by a combination of pronounced growth-stimulating and protective effects, in the regulation of wheat tolerance to water deficit. In this work, for the first time it was revealed the protective effect of 24-epibrassinolide (EBR) on wheat plants of the steppe Volga ecotype to drought, which is based on the mitigation of rapid stress-induced shifts in the content of endogenous phytohormones and the accumulation of protective protein wheat germ agglutinin (WGA). At the same time, the protective effect of EBR on plants of the forest-steppe West Siberian ecotype was not detected, which was due to preservation of stress-induced imbalance of the endogenous hormonal system and insignificant wheat germ agglutinin (WGA) accumulation. The aim of this work is to establish the role of changes in the hormonal system and the content of wheat lectin in the protective effect of 24-epibrassinolide on wheat plants of Zauralskaya Zhemchuzhina (forest-steppe West Siberian ecotype) and Ekada 70 (steppe Volga ecotype) cultivars in the initial stage of their ontogenesis under conditions of simulated soil drought. The work was conducted in 2024. Wheat seeds were pre-soaked for 3 hours in a solution of 0.4 µm of 24-epibrassinolide or distilled water (control) and sown on a soil in 15 liter pots (30 seeds per pot) and grown under controlled conditions. Then, some of the 3-day-old seedlings were exposed to early soil drought, which was modeled by limited watering until the soil moisture dropped to 30 % of the total water retention capacity of soil. In the control pots, the soil moisture was maintained at 70 % of the total water retention capacity of soil. Physiological and biochemical parameters were analyzed at the initial stage of wheat development (7-9 days). Growth was estimated by changes in the fresh and dry weights of untreated and EBR-pretreated seedlings under normal and drought conditions. The contents of abscisic acid (ABA), indolylacetic acid (IAA), cytokinins (CK) and WGA in the same 10 seedlings (0.9-1.0 g of fresh weight) on 7, 8 and 9 days were determined by enzyme immunoassay (ELISA) using specific to the studied phytohomones or WGA polyclonal rabbit antibodies and peroxidase-labeled anti-rabbit antibodies. Damage to the cell membranes of seedlings was assessed by the content of malondialdehyde (MDA), the end product of lipid peroxidation, on 9th day. It was revealed that the content of endogenous phytohormones in seedlings of Ekada 70 and Zauralskaya Zhemchuzhina cultivars underwent significant changes under drought. At the same time, more significant changes in the hormonal balance were found in the seedlings of the Zauralskaya Zhemchuzhina cultivar, which was reflected in a stronger inhibition of their growth. In conditions of drought, plants of the Ekada 70 variety were distinguished by an earlier and significantly higher accumulation of WGA (by 86% more than Zauralskaya Zhemchuzhina seedlings), which may indicate the involvement of wheat lectin in the formation of their drought tolerance. Pre-sowing EBR treatment mitigated the negative effect of drought on the growth and hormonal status of Ekada 70 seedlings during their germination under stress, which, however, was not typical for plants of the Zauralskaya Zhemchuzhina cultivar. At the same time, EBR pretreatment reduced by 30 % the stress-induced accumulation of WGA in Ekada 70 plants, which may indicate a decrease in the stress pressure on hormone-treated seedlings of this cultivar. This is supported by data on a decrease in the amount of malondialdehyde (MDA) by 26 % in the tissues of EBR-pretreated plants of the steppe Volga ecotype under drought. However, in the Zauralskaya Zhemchuzhina cultivar, the protective effect of EBR pretreatment on the content of WGA and membrane structures under stressful conditions was almost not expressed. The results obtained demonstrate the effectiveness of 24-epibrassinolide application in increasing the tolerance of wheat plants of the steppe Volga ecotype to early soil drought, whereas the weak protective effect of this phytohormone on the Zauralskaya Zhemchuzhina cultivar is apparently due to the insensitivity of plants of the West Siberian ecotype to pre-sowing EBR treatment.

Keywords: wheat, brassinosteroids, drought, hormonal balance, wheat germ agglutinin.

 

REFERENCES

  1. Munns R., Millar A.H. Seven plant capacities to adapt to abiotic stress. Journal of Experimental Botany, 2023, 74(15): 4308-4323 CrossRef
  2. Cao Y., Yang W., Ma J., Cheng Z., Zhang X., Liu X., Wu X., Zhang J. An integrated framework for drought stress in plants. International Journal of Molecular Sciences, 2024, 25(17): 9347 CrossRef
  3. Stallmann J., Schweiger R., Müller C. Effects of continuous versus pulsed drought stress on physiology and growth of wheat. Plant Biology, 2018, 20(6): 1005-1013 CrossRef
  4. Dietz K.-J., Zörb C., Geilfus C.-M. Drought and crop yield. Plant Biology, 2021, 23(6): 881-893 CrossRef
  5. González E.M. Drought stress tolerance in plants. International Journal of Molecular Sciences, 2023, 24(7): 6562 CrossRef
  6. Peer L.A., Bhat M.Y., Lone A.A., Dar Z.A., Mir B.A. Genetic, molecular and physiological crosstalk during drought tolerance in maize (Zea mays): pathways to resilient agriculture. Planta, 2024, 260(4): 81 CrossRef
  7. Tsigankov V.I. Izvestiya Orenburgskogo gosudarstvennogo agrarnogo universiteta, 2011, 2(30): 46-50 (in Russ.).
  8. Mukhitov L.A., Samuilov F.D. Vestnik Kazanskogo gosudarstvennogo agrarnogo universiteta, 2014, 9(3): 135-138 (in Russ.).
  9. Hong J.H., Seah S.W., Xu J. The root of ABA action in environmental stress response. Plant Cell Reports, 2013, 32: 971-983 CrossRef
  10. Zhang C., Wu F., Yan Q., Duan Z., Wang S., Ao B., Han Y., Zhang J. Genome-wide analysis of the Rab gene family in Melilotus albus reveals their role in salt tolerance. International Journal of Molecular Sciences, 2022, 24(1): 126 CrossRef
  11. Avalbaev A., Bezrukova M., Allagulova C., Lubyanova A., Kudoyarova G., Fedorova K., Maslennikova D., Yuldashev R., Shakirova F. Wheat germ agglutinin is involved in the protective action of 24-epibrassinolide on the roots of wheat seedlings under drought conditions. Plant Physiology and Biochemistry, 2020, 146: 420-427 CrossRef
  12. Jiang S.Y., Ma Z., Ramachandran S. Evolutionary history and stress regulation of the lectin superfamily in higher plants. BMC Evolutionary Biology, 2010, 10: 79 CrossRef
  13. Kumar D., Shekha S, Bisht S., Kumar V., Varma A., Kumar M. Ectopic overexpression of lectin in transgenic Brassica juncea plants exhibit resistance to fungal phytopathogen and showed alleviation to salt and drought stress. Journal of Bioengineering and Biomedical Science, 2015, 5: 147 CrossRef
  14. Faysal Ahmed F., Dola F.S., Zohra F.T., Rahman S.M., Konak J.N., Sarkar M.A.R. Genome-wide identification, classification, and characterization of lectin gene superfamily in sweet orange (Citrus sinensis L.). PLoS One, 2023, 18(11): e0294233 CrossRef
  15. Bogoeva V.P., Radeva M.A., Atanasova L.Y., Stoitsova S.R., Boteva R.N. Fluorescence analysis of hormone binding activities of wheat germ agglutinin. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics, 2004, 1698(2): 213-218 CrossRef
  16. Shakirova F.M., Kildibekova A.R., Bezrukova M.V., Avalbaev A.M. Wheat germ agglutinin regulates cell division in wheat seedling roots. Plant Growth Regulation, 2004, 42: 175-180 CrossRef
  17. Bezrukova M., Kildibekova A., Shakirova F. WGA reduces the level of oxidative stress in wheat seedlings under salinity. Plant Growth Regulation, 2008, 54: 195-201 CrossRef
  18. Wei Z., Li J. Brassinosteroids regulate root growth, development, and symbiosis. Molecular Plant, 2016, 9(1): 86-100 CrossRef
  19. Khan T.A., Kappachery S., Karumannil S., AlHosani M., Almansoori N., Almansoori H., Yusuf M., Tran L.P., Gururani M.A. Brassinosteroid signaling pathways: insights into plant responses under abiotic stress. International Journal of Molecular Sciences, 2023, 24(24): 17246 CrossRef
  20. Zebosi B., Vollbrecht E., Best N.B. Brassinosteroid biosynthesis and signaling: conserved and diversified functions of core genes across multiple plant species. Plant Communications, 2024, 5(9): 100982 CrossRef
  21. Shakirova F.M., Bezrukova M.V., Aval’baev A.M., Gimalov F.R. Fiziologiya rasteniy, 2002, 49: 253-256 (in Russ.).
  22. Bezrukova M.V., Aval’baev A.M., Kil’dibekova A.R., Fatkhutdinova R.A., Shakirova F.M. Dokladi Rossiyskoy akademii nauk, 2002, 387: 276-278 (in Russ.).
  23. Shakirova F.M., Bezrukova M.V. Fiziologiya rasteniy, 1998, 42: 451-455 (in Russ.).
  24. Sharipova G.V., Veselov D.S., Kudoyarova G.R., Timergalin M.D., Wilkinson S. Fiziologiya rasteniy, 2012, 59: 619-626 (in Russ.).
  25. Metodicheskie rekomendatsii po gigienicheskomu obosnovaniyu PDK khimicheskikh veshchestv v pochve [Methodological recommendations for the hygienic justification of MAC of chemical substances in soil]. Moscow, 1982 (in Russ.).
  26. Batigina T.B. Khlebnoe zerno: atlas [Bread grain: atlas]. Leningrad, 1987 (in Russ.).
  27. Hong Z., Lakkineni K., Zhang Z., Verma D.P.S. Removal of feedback inhibition of Δ1-pyrroline-5-carboxylate synthetase results in increased proline accumulation and protection of plants from osmotic stress. Plant Physiology, 2000, 122(4): 1129-1136 CrossRef
  28. Avalbaev A.M., Yuldashev R.A., Allagulova Ch.R., Plotnikov A.A., Lastochkina O.V. Drought tolerance of wheat Triticum aestivum L. plants differing in the drought adaptation strategies during early ontogenesis. Sel'skokhozyaistvennaya biologiya [Agricultural Biology], 2024, 59(1): 131-141 CrossRef
  29. Llanes A., Andrade A., Alemano S., Luna V. Alterations of endogenous hormonal levels in plants under drought and salinity. American Journal of Plant Sciences, 2016, 7(9): 1357-1371 CrossRef
  30. Li S.-M., Zheng H.-X., Zhang X.-S., Sui N. Cytokinins as central regulators during plant growth and stress response. Plant Cell Reports, 2021, 40(2): 271-282 CrossRef
  31. Rathor P., Upadhyay P., Ullah A., Gorim L.Y., Thilakarathna M.S. Humic acid improves wheat growth by modulating auxin and cytokinin biosynthesis pathways. AoB Plants, 2024, 16(2): plae018 CrossRef
  32. Allagulova C., Avalbaev A., Lubyanova A., Plotnikov A., Yuldashev R., Lastochkina O. Nitric oxide (NO) improves wheat growth under dehydration conditions by regulating phytohormone levels and induction of the expression of the TADHN dehydrin gene. Plants, 2023, 12(23): 4051 CrossRef
  33. Shakirova F.M., Bezrukova M.V., Shayakhmetov I.F. Effect of temperature shock on the dynamics of abscisic acid and wheat germ agglutinin accumulation in wheat cell culture. Plant Growth Regulation, 1996, 19: 85-87 CrossRef
  34. Singh P., Bhaglal P., Bhullar S. Wheat germ agglutinin (WGA) gene expression and ABA accumulation in the developing embryos of wheat (Triticum aestivum) in response to drought. PlantGrowthRegulation, 2000, 30: 145-150 CrossRef

 

back

 


CONTENTS

 

Full article PDF (Rus)